<?xml version="1.0" encoding="utf-8"?>
<source><publisher>Team Horizon</publisher><company>Team Horizon</company><publisherurl>http://www.teamhorizon.ie/</publisherurl><job><title><![CDATA[Recruitment Consultant]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2021-11-01 11:35:17]]></date><referencenumber><![CDATA[303]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=303&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Are you an outgoing, highly organised person who enjoys helping people find their dream job. If you are an experienced recruiter looking to develop your skills beyond what you expected within an amazing company, we are looking for you!
&amp;nbsp;
Why you should apply:

	
		Every day is different and you can enjoy supporting a range of roles.
	
		The role is generously compensated, and attracts a competitive base salary.
	
		Excellent career progression opportunities.

&amp;nbsp;
What you will bedoing:

	
		Working with clients and hiring managers looking at current and future recruitment requirements
	
		Developing sourcing strategies to attract and promote top talent
	
		Leading interviews for key partners
	
		Partnering with hiring managers on complete recruiting life cycle
	
		Communicating with candidates to ensure efficiency and ongoing brand awareness
	
		Working with clients in identifying the right fit candidates
	
		Executing sourcing strategies for talent pipeline campaigns


What you need to apply:

	
		Relevant 3rd level qualification
	
		2+ years recruitment experience either in house or with a 3rd party agency
	
		Pharma industry related experience is preferred
	
		Brilliant communications skills
	
		Customer focused attitude
	
		Ability to engage with multiple customers
	
		Remote working experience
	
		Great relationship building skills

]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[Senior MES Automation Integration Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2022-04-11 18:39:54]]></date><referencenumber><![CDATA[499]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=499&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Senior MES Automation Integration&amp;nbsp;Specialist &amp;ndash; Team Horizon
We are now recruiting a Senior MES Automation Integration Specialist to be part of our team on our client&amp;rsquo;s pharmaceutical site in Sligo. You would be responsible for aligning technology solutions with business strategies around integration of Manufacturing Execution Systems (MES). You will be working with senior management to drive LRP Roadmap and Standardization of the integration efforts with the sites engineers and system owners. Acts as the principal designer for major systems and their subsystems utilizing a thorough understanding of available technology, tools, and existing designs. As a member of the global BTS Manufacturing Operations team, you will be helping define standards/best practices for integration, working with site and vendor resources to identify requirements, trends, and new capabilities.
Why you should apply:

	
		Our client has developed a stand-out culture of innovation, inclusion, and development, and consistently features as a great place to work.
	
		The role is generously compensated and attracts a competitive base salary and highly attractive benefits package.
	
		Excellent career progression opportunities.

&amp;nbsp;
What you will bedoing:

	
		Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
	
		Serve as technical expert or lead projects/programs and technical staff to develop, test and implement significant new products, or operational improvements or devise new approaches to problems at the division/business unit.
	
		Conduct investigation activity/research and give technical advice to the adoption or integration of new technologies and their business impact.
	
		Lead in the development of standards and procedures and publish/communicate findings via IOI&amp;rsquo;s, presentations, white papers, etc.
	
		Review, validate &amp;amp; enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.
	
		Partner with the functional groups within the IT organization to communicate and clarify business needs, contribute to development of long-range system plans, and ensure products and services are aligned with business needs.
	
		Provides strategic consultancy support to customers in defining or designing business processes and researching and identifying enabling technologies based on customer requirements.
	
		Actively seek ways to apply technology to business processes, researching and providing information on technical trends and competitors&amp;#39; practices relevant to the assigned client business.
	
		Ally with other IT functional areas to remain apprised of project status, and inform customer management of progress; conversely, keep the IT group&amp;#39;s technology and service managers aware of user issues and potential potholes or resolve conflicts.
	
		Develop, motivate, and provide direction to technical team in a way that facilitates the creation of a team environment and enables team to fulfill the department&amp;#39;s operation objectives.
	
		Accountable for total project scope, budget, completion within budget constraints and schedules completion date.
	
		Accountable for successful and timely completion of all tasks/projects under direct and matrix control.
	
		Post completion audit of project after implementation to verify expected benefits vs. costs, both development and operating.
	
		Project success is critical to the continued business success of the corporation.

What you need to apply:

	
		Four-year degree or equivalent experience in Process Control Engineering, Manufacturing Execution Systems (MES), Information Technology, Computer Science or Computer engineering. Equivalent experience is defined as six years combined experience in the above areas.
	
		5-8 years of combined experience in Process Control System Integration (in addition to equivalent experience listed above, if applicable).
	
		Experience with MES/POMSnet, OSI-PI Historian (or equivalent data historian) or DeltaV and/or Foxboro Distributed Control System (DCS) (or equivalent DCS systems) preferred.

]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific, IT/Software]]></category></job><job><title><![CDATA[CAD Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2024-06-04 16:44:15]]></date><referencenumber><![CDATA[1354]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1354&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[







3315 - CAD Engineer
 
Team Horizon has an opportunity for a CAD Engineer. An experienced CAD Engineer is required to support our clients design effort for their manufacturing facility. The successful candidate will be motivated, driven and be capable of working effectively in a pressured team environment.
 
Why you should apply:

Opportunity to work with cutting edge technology in a high performance work environment
Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Sligo.

 
 
What you will be doing:

Adherence to the site safety and quality systems at all times.
Management of Drawing Management system, for the site.
Create new and update existing site drawings using AutoCAD.
2-3 years AutoCAD experience.
Will support day-to-day and projects work.
Needs to be proficient in AutoCAD, background in pharma or Engineering Consultancy ideally.
Quality and safety focused with an understanding of electro/mechanical systems and the ability to understand drawings.
Ability to work in a fast paced regulated and project environment.
Excellent timekeeping and attention to detail.
Any other duties as required

 
What you need to apply:

Relevant AutoCAD Qualification
A minimum of 2 years of experience in a relevant industry at an equivalent position.
Strong IT knowledge is required. 
Strong documentation skills.








]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Associate Director, Technical Product Development Science &amp; Tech]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2024-11-12 09:35:32]]></date><referencenumber><![CDATA[1448]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1448&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking an Associate Director, Technical PDS&amp;T for our client based in Mayo. The Product Development Science &amp; Technology (PDS&amp;T) organization will lead the PDS&amp;T Analytical organization at Mayo Ireland, and is responsible for providing technical leadership, direction and management of the Analytical PDS&amp;T team and global initiatives and development programs.
The Analytical PDS&amp;T team develops, validates, transfers and maintains analytical methods for New Biological Entities and marketed products and defines global analytical strategies. The Associate Director leads these activities using state-of-the-art development approaches resulting in high-performing and robust analytical methods that ensure successful late-stage development for pipeline programs, submission of global regulatory filings and assurance of supply of on-market products.
The Associate Director recruits and manages department personnel, sets priorities, and manages employee development. The Associate Director ensures that the function’s deliverables are completed within established timelines, budgets, resource allocation and in accordance with regulatory, quality, and safety requirements.
 
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

The Associate Director provides technical leadership for multiple late-phase pipeline projects and commercial products that are marketed globally.
Guiding cross-functional late-stage development and validation of analytical methods, global method transfers to troubleshooting and life-cycle management of test methods used for commercial products.
The portfolio of analytical technologies includes physico-chemical methods but also complex cell-based potency assays.
Leads and supports global and local project teams, liaises with early development functions in R&amp;D, interacting with other functions in Operations, Regulatory as well as relevant technical plant functions.
Leads activities executed at global external partners (CDMOs, Third-party laboratories) and method transfers to global regulatory agency laboratories.
The Associate Director leads global initiatives, defines CMC/analytical strategies for global product development programs and can represent the company in discussions with various regulatory agencies. 
Due to nature of the projects and support of marketed products, the impacts of decisions are significant to pharmaceutical Operations to ensure successful regulatory filings and global market launches and to minimize regulatory risks and back orders.
Managing a team of scientists ranging from scientist to principal level scientists which includes goal setting, performance management, people development, promotion recommendations and salary management.
Responsibility/ownership for content of quality and global regulatory submission documents, responses to health agency requests and post approval filings.
Perform financial planning and execute budget responsibility.

 
What you need to apply:

BSc degree in a scientific or technical field preferably in Life sciences, chemistry or pharmacy required. Masters degree and/or PhD is preferred. The following combinations of education and experience are required:  BSc and 10+ years of experience; or MSc and 6+ years of experience; or PhD and 4+ years of experience. Must have 4+ years of experience in pharmaceutical industry in the field of analytical chemistry preferably for CMC development of biological products.
Must have a record of demonstrated successful development or commercialization of products. Expertise with development of cell-based bioassays and modern analytical development approaches per ICH-Q14, and statistics skills are a plus.
Sound knowledge of applicable global regulations and standards affecting Pharmaceutical Products (e.g. CFR 210/211, cGMP).
Must display managerial ability via leadership, supervisory experience and administration in a cross-functional and global setting.
Previous experience in leading people is required. Has strong management and long-term planning skills. Must be goal oriented, able to work within a team environment, self-motivated and understand the business needs to meet timelines.
Able to work in a fast-paced, multi-disciplinary and dynamic environment with potential for changing priorities, with flexibility to support multiple development programs simultaneously.
Very good verbal and written communication skills and the ability to interface with multiple areas within a global organization are essential.

 
 ]]></description><salary><![CDATA[Upto £10,000]]></salary><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Management, Laboratory/Scientific]]></category></job><job><title><![CDATA[Visual Inspections Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-05-07 12:15:25]]></date><referencenumber><![CDATA[1566]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1566&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Visual Inspections Engineer
 Team Horizon is seeking a Visual Inspections Engineer for a Visual Inspections Engineer. This person will be responsible for supporting strategy to qualify samples /streamlining processes and taking part in threshold studies.
 Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 What you will be doing:

To work as a team member to support Visual Inspection operations in line with all safety, regulatory and organizational requirements.
Develop and modify procedures as needed to support the manufacturing operation.
Participate in process, equipment, and facilities validations efforts and projects implementations.
Review and approve process related commissioning, qualification and validation protocols for completeness and accuracy.
Execute protocols in a timely basis to meet the project schedule requirements.
Participate and lead (as required) Process FMEAs for Visual Inspection
Establish, Lead and Optimize the process for certification of technicians for visual inspection.
Establish and maintain the defect library.
Establish and execute the process for the trending of Visual Inspection Defects
 Ensure all Site Visual Inspection procedures are aligned with Global Guidance Documents and Regulatory Requirements
Provide Technical Input to guide the development of SOPs for Visual Inspection.
Leadership of manufacturing and validation activities during project life cycle.
Coordination with internal/external stakeholders for the evaluation of particles/defects
Support of technical transfers for future product introductions to the site.
Investigate process exceptions or malfunction incidents affecting the process.
To liaise with Internal/External Engineering Personnel and Internal/External Quality personnel as required.
Support the Production Team in ensuring that manufacturing process is enabled and maintained to meet the output and yield requirements.
May be required to support Cross functional teams and cost improvement projects.
 Provide technical leadership to functional areas and collaborates with key stakeholders.
 Leads the delivery of new training initiatives

 What you need to apply:

A relevant third level qualification in an engineering, science or technical discipline (Degree Level or Masters Preferable)
At least three (3) years of total combined experience in Technical/Operations/Operations/Quality or equivalent in a Pharmaceutical and Health Care Organization.
At least three (3) years of experience in the manufacturing environment of a biotechnology, pharmaceutical or health care plant.
Previous experience in manufacturing processes of biotechnological drugs, parenteral drugs, solutions preparation, fill finish, Lyophilisation, sterilisation operations preferable. 
 Experience in clean utilities is desirable.
Requires a very high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders.
Understands and supports the principles of Perfect Performance.
 Requires good knowledge of Company Policies and Procedures and involves working towards general results to achieve organizational needs.
Expected to handle all day-to-day training, learning &amp;amp; development queries, if major problem can refer to Team Manager.
Comply with the EHS policy and procedures and demonstrate EHS best practices in all work activities.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Project Coordinator ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-05-20 12:01:55]]></date><referencenumber><![CDATA[1580]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1580&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Coordinator for our client’s manufacturing facility in Sligo. In this role you will manage the development and implementation process of the company's products and services involving cross-functional teams focused on the delivery of new products.
 
 
Why you should apply:

This is an exciting opportunity to join a leading biopharmaceutical manufacturing company who work across several therapeutic areas.
Excellent opportunity to leverage your organisation and project management experience by providing admin support to facilitate meetings, work with the SME to identify tasks and timelines, set up tasks and meeting follow ups, &amp;amp; identify critical path.

 
What you will be doing:

Manages the development and implementation process of company's products and services involving cross-functional teams focused on the delivery of new products.
Estimates project levels of effort and resource requirements by using standard estimating techniques and tools, and by working with appropriate staff to understand scope of effort.
Prepares project plans, schedules and budgets by using project management tools such as Microsoft Project and by working with appropriate staff to understand tasks necessary to complete project.
Directs project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans.
Assures project quality by using standard development methodologies and by working with SQA to develop and execute project quality plans.
Communicates project status by preparing standard status reports, and by leading and participating in departmental and customer project status update meetings.
Resolves project issues by working with team members, project customers (internal and external), and others as appropriate.
Consults with internal project groups by sharing project management knowledge and assisting other project team stakeholders in project management processes and techniques.
Responsible to raise Change Plan: drive impact assessment, present CP to CFT meetings and drive approval up to Change review board
Prepares, edits, files, assembles documentation such as reports or technical documents, records, or correspondence.
Maintains numerical, alphabetical, chronological and/or subject filing system.
Responsible for file maintenance and record keeping; locates and removes file material upon request.

 
What you need to apply:

Degree plus 5 years of related work experience with a good understanding of specified functional area
Working technical knowledge and application of concepts, practices and procedures. General understanding of business unit/group function.
Will perform this job in a quality system environment.
Failure to adequately perform tasks can result in noncompliance with governmental regulations. 
Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors.
Exercises judgment within defined procedures and practices to determine appropriate action.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[QP (Qualified Person) ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-05-22 17:14:19]]></date><referencenumber><![CDATA[1588]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1588&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QP for our Clients manufacturing facility in the West of Ireland. In this role you will be responsible for ensuring the compliance and quality of pharmaceutical products. This role requires expertise in quality assurance practices within an FDA and EMEA approved environment to maintain product safety and integrity.
As a QP for the site, you will work closely with our products throughout their manufacturing lifecycle, up until release from the site.
 
Why you should apply:

This is an excellent opportunity to join a company who put their people &amp;amp; their patients first.
You will have the resources and a global reach to empower your innovative mindset and make ground-breaking advancements happen.
Make a lasting impact that's felt within healthcare and beyond.

 
 
What you will be doing:

Ensure compliance with EudraLex Volume 4 EU Guidelines for Good Manufacturing Practice and Annex 16 requirements.
Certify that each batch is manufactured and checked according to relevant laws, GMPs, and product specifications
Oversee the disposition of bulk products, determining release or rejection based on manufacturing and testing data.
Assess and resolve day-to-day quality issues, ensuring products meet quality and safety standards.
Support cross-functional teams in process improvement and cost efficiency initiatives.
Provide technical leadership and collaborate with stakeholders to enhance product quality and process optimization.
Make informed decisions within quality systems, adhering to regulatory standards, and handle quality queries from the operations team.
Promote a culture of excellence in quality and compliance throughout the organization.
Participate in internal and external audits, ensuring readiness and compliance with quality standards.

 
What you need to apply:

Bachelor's degree in a science discipline and a minimum of 5 years of experience in the pharmaceutical industry.
MSc in Industrial Pharmaceutical Science or equivalent recognized for QP status under Directive 2001/83/EC, Article 49.
Experience as a QP on a license preferrable
Experience in aseptic processing and quality functions.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Validation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-05-28 16:02:52]]></date><referencenumber><![CDATA[1591]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1591&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Validation Engineers our client’s facility. In this role, you will be responsible for delivering on the qualification and validation program, which will include planning and execution of validation/requalification activities on critical equipment.
 
Why you should apply:

Join a fast paced and diverse team, in a company who are committed to  discovering, developing, &amp;amp; manufacturing innovative human therapeutics
Flexibility around remote working when the role allows

 
What you will be doing:

In this role, you will be responsible for delivering on the qualification and validation program which will include planning and execution of validation/requalification activities on critical equipment.
Provide technical validation support to meet site objectives, comprising the full validation lifecycle process.
Develop, review, and approve validation plans, protocols, and discrepancy summary reports. Lead the execution of airflow visualization, filter integrity, velocity, and particle monitoring testing activities
Lead the execution of cycle development, performance qualifications, and requalification programs for VPHP isolators.
Collate and report relevant validation data and metrics.
Assist in the development and improvement of the validation lifecycle process while ensuring compliance with all applicable regulations and standards.
Provide validation support for quality management system, including change control, deviation, and CAPA processes.
Coordinate projects and prioritize workload in line with site priorities.
Participate in multidisciplinary site and multisite teams, such as cross-functional investigation teams and change control
Update and maintain validation Standard Operating Procedures (SOPs) in accordance with site and corporate requirements.
Attend and contribute to staff meetings and training sessions as required.
Comply with the responsibilities outlined in the Site Safety Statement and champion safe working practices.
Perform all tasks with due care and attention in accordance with Good Manufacturing Practices and  requirements, policies, and procedures.

 
What you need to apply:

Bachelor of Science/Engineering degree or equivalent.
Knowledge of cGMPs and other worldwide regulatory requirements.
Problem-solving ability and excellent oral and written communication skills
5+ years’ experience in a similar role. 
Experience qualifying HVAC systems and/or executing VPHP qualifications.
Familiarity with Quality and Document Management Systems, including Trackwise Deviations, CAPA and Change Controls, Maximo, CDOCs, Kneat.
Independent, self-motivated, proactive, organized, able to multi-task in project environments, and skilled in communication and collaboration.
Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineers]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-06-11 13:02:06]]></date><referencenumber><![CDATA[1601]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1601&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Validation Engineer
 
Team Horizon is seeking a Validation Engineers for a leading pharmaceutical company in South Dublin.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Validation Engineer responsible for ensuring that the Validation activities associated with a Syringe Filling Line for a Sterile fill finish facility are in compliance with GMP and Quality Requirements.
Generation, execution, review and approval of CQV test Documentation (Factor Acceptance Testing (FAT), Instillation Verification (IV’s), Functional Testing (FT’s), Site Acceptance Testing (SAT) and Performance Qualifications (PQ’s) associated with a Syringe Filling Line.
Pre-Approve and Post-Approve validation protocols.
Input into site Validation Master Plans and Standard Operating Procedures (SOP’s)
Collate and Report on relevant validation data/metrics.
Assist in exceptions and deviation resolution and root cause analysis.
Reviews Validation planning documents detailing overall strategy for the project.
Reviews and Approves Qualification summary reports (QSR)
Generates Validation Summary reports.
Assist in the development of User Requirement Specifications (URS’s) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).
Any other duties as assigned.

 
What you need to apply:

6+ years experience in Engineering or Validation Technical qualification at third level or equivalent in Engineering.
Extensive knowledge and demonstrated experience executing Validation activities for Pharmaceutical / Biotechnology projects Experience of sterile / biotech equipment within the pharmaceutical industry is preferred.
Knowledge of safety and GMP requirements.
Demonstrated strong Communication skills.
Experience using Paperless Qualification Systems is preferred.
Strong understanding of a risk-based approach to commissioning, qualification and validation within the biotechnology industry
]]></description><salary><![CDATA[Upto £10,000]]></salary><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior MES Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-07-08 12:16:16]]></date><referencenumber><![CDATA[1620]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1620&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Senior MES
 
Team Horizon is seeking a Senior MES Engineer for our client who are a global leader in the biopharmaceutical industry for their Mayo site.
 
The purpose of this role is to Maintain the MES (POMSnet) environment; to author and maintain recipes and worksheets and providing technical guidance and solutioning to the other MES Engineers. The MES Engineer will also Act as site escalation point for complex or challenging troubleshooting or recipe design. As well as providing project management guidance and expertise to the MES function.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
 
What you will be doing:

Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material spec's including phase transition logic
Design, create, write and execute, test and validation protocols, risk assessments, and system documentation.
Design, create, write and/or make all required changes to ensure cleaning, equipment and product procedures are aligned to MES processes and vice versa.
Design, create, write and provide training for all other site personnel on their related MES roles and arrange system access.
Participate in MES knowledge exchanges, MES Governance meetings, and manage issues, work-arounds and fixes identified.
Liaise with the Global MES on the sites required system improvements.
Provide support to other MES system users as required to ensure business continuity.
Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.
Keep other recipe authors up to date on MES changes
Documentation of all activities in line with cGMP requirements.
Cross training within the team and training of new team members.
Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
Adheres to and supports all EHS standards, procedures and policies. 

 
What you need to apply:

Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.
A minimum of 7 years authoring experience and has led or was technical lead on multiple implementation projects.
Be proficient with MES application and configuration rules and requirements including interfacing (preferably POMSnet).
Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.
A good knowledge of IT systems is required for this role.
SAP knowledge/experience in MM, PP and IM modules.
Proven attention to detail and mental concentration, to always ensure total compliance with procedures.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[IT/Software]]></category></job><job><title><![CDATA[Micro Analyst]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-07-10 16:35:05]]></date><referencenumber><![CDATA[1621]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1621&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QC Microbiology (Senior) for our client based in Dublin. The successful candidate would contribute to team by ensuring the quality of the tasks/services provided by self and contribute to the completion of milestones associated with specific projects or activities within team. 
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Endotoxin testing of water, in-process and drug product release samples
Bioburden testing of water &amp;amp; in-process drug product samples
Sterility testing
Water sampling
Lab Support duties such as Biological Indicator testing, Growth Promotion, Media Preparation,

Identifications and Autoclave.

Writing technical reports
Media fill reconciliation and inspection
Weekend bioburden cover
Perform analytical testing as a main priority with efficiency and accuracy
Report, evaluate, archive, trend and approve analytical dat
Troubleshoot, solve problems and communicate with stakeholders
Initiate and/or implement changes in controlled documents
Participate in audits, initiatives, and projects that may be departmental or organizational in scope
Write protocols and perform assay validation
Introduce new techniques to the lab, including method transfers, reports, validations and protocols.?

 
What you need to apply:

Bachelors degree in a science discipline
Biopharmaceutical QC experience in a microbiology lab?
Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products? 

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Sr Associate QC (Senior)]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-08-19 15:59:48]]></date><referencenumber><![CDATA[1638]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1638&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Sr Associate QC (Senior) for our client in Dublin.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Planning and conducting routine calibration, requalification and maintenance of laboratory equipment ensuring calibration and maintenance schedules are adhered to as per CMMS Maximo.
Reviewing &amp;amp; filing of QC calibration &amp;amp; maintenance documentation.
Planning, executing and documenting the qualification of new laboratory equipment in a cGMP regulated environment, including the writing of equipment validation protocols and associated summary reports.
Conduct periodic reviews of instrument validation as part of validation life cycle.
Alerting Quality Control Management in the event of equipment failing to meet calibration or qualification requirements and conducting impact assessments/investigations as required
Scheduling and coordination of equipment repairs and maintenance with vendors/contractors, while minimizing level of down-time for lab equipment, and disruption to laboratory activities.
Participation in technical project teams to act as a subject matter expert on instrument validation regulations and procedures.
Where applicable, owns and project manages change controls and adherence to Change Control metrics
Supporting and managing the addition of project components to CMMA Maximo
Act as a key contributor and sponsor to Data Integrity Assessments for Lab systems
Any other tasks/projects assigned as per manger’s request

 
What you need to apply:

Bachelor’s degree in a Science related field is required.
Minimum of 3 years of laboratory experience in a cGMP laboratory environment including exposure to analytical instrument validation and data integrity assessments.
Detailed knowledge of the methodology, and instrumentation and analytical techniques used for biopharmaceutical testing.
Understanding of current regulatory requirements for cGMP laboratory equipment validation and electronic record integrity.
Demonstrated success in managing an equipment qualification or maintenance program advantageous.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Technical Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-08-28 09:16:25]]></date><referencenumber><![CDATA[1645]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1645&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a ADC Technical Manager for our client based in Sligo. We are looking for an ADC Technical Manager to provide technical support and day-to-day program management to all new product introductions (NPIs) sitewide across 3 departments. Reports to  the Technical Operations Manager. The successful candidate will provide team leadership to the NPI product team, process team and ADC team. This is an exciting time to join the team as we continue to introduce new products and innovation.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Lead and support NPI activities for product, processes and technology from early-stage development through to PPQ.
Lead and manage cross functional teams across different skillsets and disciplines to perform activities required to deliver NPI's.
Collaborate with cross functional teams including Process Development, Science &amp;amp; Technology (PDS&amp;amp;T), Quality, Manufacturing, Supply Chain and ECM to facilitate the smooth transition of new products from development to commercialization.
Complete all site fit assessments for all the products from pipeline and ECM opportunities
Provide technical direction and oversight and coordinate support for NPI activities across the entire biological manufacturing area
Work closely with internal and external program management to ensure alignment on NPI schedules
Ensure resource availability for all NPI related activities
Build and maintain a mindset of innovation and continuous improvement withing the function.
Provide leadership and mentoring for operations personnel during NPI activities
Collaborate with external parties to ensure engagement and alignment and open communication throughout NPI activities
Engage with external and internal partners to influence the design and implementation of robust process control strategies on process risk assessments
Generate product transfer documentation to attest the completion of product transfer deliverables in advance of the application product transfer stage gate review provide technical input, review\ approval for documentation associated with NPI activities
Ensure ongoing compliance with CGMP and EHS practices new
Participate in NPI project gate reviews Interface with internal auditors and outside regulatory agencies\ auditors as the subject matter expert for new products and technology transfers

 
What you need to apply:

Ph.D in Chemistry, Biochemistry, Chemical Engineering or related field Minimum 10 years experience in pharmaceutical or biotechnology industry
Proven strategic leadership experience with the ability to inspire and motivate a diverse and global team.
Extensive experience from working in an international organisation and across borders.
Extensive and in-depth knowledge about clinical and commercial manufacturing, CMC process and analytical development.
CMC technical lifecycle management In-depth understanding of regulatory and quality requirements in relevant area
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[QA Specialist - Supplier &amp; Vendor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-04 16:34:05]]></date><referencenumber><![CDATA[1649]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1649&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Specialist to join our client’s team on a permanent basis. In this role you will have responsibility for GxP Supplier and Vendor Oversight.
 
 
Why you should apply:

Opportunity to be part a diverse team and an established company which offer career progression opportunities.
They put their people first and live their diversity and inclusion values embracing all perspectives.
Competitive salary &amp;amp; benefits package.

 
 
What you will be doing:

Act as the global QA SME for qualification and oversight of GxP-relevant suppliers, including GMP, GLP, GCP, GDP etc., service providers.
Lead the development, implementation, and continuous improvement of the supplier qualification program, including risk-based classification, audit planning, and ongoing performance monitoring.
Conduct supplier audits (initial, routine, for-cause), prepare audit reports, track CAPAs, and verify implementation effectiveness.
Review and approve supplier quality documentation, such as Technical/Quality Agreements, audit responses, change notifications, and deviation reports.
Evaluate supplier quality systems and compliance with applicable international regulatory requirements (e.g., EMA, OECD GLP, VICH GCP, ISO/IEC 17025, HACCP, etc.).
Provide QA input into procurement decisions and cross-functional sourcing teams to ensure GxP compliance is considered in supplier selection.
Support internal stakeholders (e.g., R&amp;amp;D, Manufacturing, QC, Regulatory Affairs, Procurement) in supplier-related investigations and risk assessments.
Develop and deliver internal training on supplier qualification procedures and regulatory expectations.
Represent QA in cross-functional teams involving outsourced activities, ensuring the integrity of GxP-related data and deliverables.
Maintain accurate and current records in eQMS systems and supplier management databases.

 
What you need to apply:

Bachelor’s degree or higher in Life Sciences, Pharmacy, Biotechnology, or a related scientific discipline.
Minimum of 7–10 years of QA experience in the pharmaceutical, biologics, or veterinary vaccine industry.
At least 5 years of hands-on experience in GxP supplier qualification and auditing, with demonstrated expertise in GMP and at least one of the following: GLP, GCP, GDP.
Experience with laboratory testing, contract manufacturing, and/or clinical service providers preferred.
Proficiency in English (written and oral); additional languages are an asset.
Solid knowledge of EU GMP, FDA regulations, OECD GLP, VICH GCP, and ICH guidelines.
Proven ability to plan, conduct, and report external audits independently.
Strong understanding of quality systems, technical agreements, and risk-based approaches to supplier qualification.
Experience with quality investigations, CAPA management, and change control.
Proficiency with QMS tools, audit tracking systems, and MS Office; experience with eQMS platforms preferred.
Critical thinking, strong attention to detail, and ability to interpret complex regulations into operational requirements.
Excellent communication and interpersonal skills; capable of engaging with diverse stakeholders globally.
Willingness to travel domestically and internationally up to 25%

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[QA Specialist - Supplier &amp; Vendor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-04 16:34:05]]></date><referencenumber><![CDATA[1649-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1649&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Specialist to join our client’s team on a permanent basis. In this role you will have responsibility for GxP Supplier and Vendor Oversight.
 
 
Why you should apply:

Opportunity to be part a diverse team and an established company which offer career progression opportunities.
They put their people first and live their diversity and inclusion values embracing all perspectives.
Competitive salary &amp;amp; benefits package.

 
 
What you will be doing:

Act as the global QA SME for qualification and oversight of GxP-relevant suppliers, including GMP, GLP, GCP, GDP etc., service providers.
Lead the development, implementation, and continuous improvement of the supplier qualification program, including risk-based classification, audit planning, and ongoing performance monitoring.
Conduct supplier audits (initial, routine, for-cause), prepare audit reports, track CAPAs, and verify implementation effectiveness.
Review and approve supplier quality documentation, such as Technical/Quality Agreements, audit responses, change notifications, and deviation reports.
Evaluate supplier quality systems and compliance with applicable international regulatory requirements (e.g., EMA, OECD GLP, VICH GCP, ISO/IEC 17025, HACCP, etc.).
Provide QA input into procurement decisions and cross-functional sourcing teams to ensure GxP compliance is considered in supplier selection.
Support internal stakeholders (e.g., R&amp;amp;D, Manufacturing, QC, Regulatory Affairs, Procurement) in supplier-related investigations and risk assessments.
Develop and deliver internal training on supplier qualification procedures and regulatory expectations.
Represent QA in cross-functional teams involving outsourced activities, ensuring the integrity of GxP-related data and deliverables.
Maintain accurate and current records in eQMS systems and supplier management databases.

 
What you need to apply:

Bachelor’s degree or higher in Life Sciences, Pharmacy, Biotechnology, or a related scientific discipline.
Minimum of 7–10 years of QA experience in the pharmaceutical, biologics, or veterinary vaccine industry.
At least 5 years of hands-on experience in GxP supplier qualification and auditing, with demonstrated expertise in GMP and at least one of the following: GLP, GCP, GDP.
Experience with laboratory testing, contract manufacturing, and/or clinical service providers preferred.
Proficiency in English (written and oral); additional languages are an asset.
Solid knowledge of EU GMP, FDA regulations, OECD GLP, VICH GCP, and ICH guidelines.
Proven ability to plan, conduct, and report external audits independently.
Strong understanding of quality systems, technical agreements, and risk-based approaches to supplier qualification.
Experience with quality investigations, CAPA management, and change control.
Proficiency with QMS tools, audit tracking systems, and MS Office; experience with eQMS platforms preferred.
Critical thinking, strong attention to detail, and ability to interpret complex regulations into operational requirements.
Excellent communication and interpersonal skills; capable of engaging with diverse stakeholders globally.
Willingness to travel domestically and internationally up to 25%

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[QA Specialist - Supplier &amp; Vendor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-04 16:34:05]]></date><referencenumber><![CDATA[1649-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1649&amp;Itemid=986]]></url><city><![CDATA[Leitrim]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Specialist to join our client’s team on a permanent basis. In this role you will have responsibility for GxP Supplier and Vendor Oversight.
 
 
Why you should apply:

Opportunity to be part a diverse team and an established company which offer career progression opportunities.
They put their people first and live their diversity and inclusion values embracing all perspectives.
Competitive salary &amp;amp; benefits package.

 
 
What you will be doing:

Act as the global QA SME for qualification and oversight of GxP-relevant suppliers, including GMP, GLP, GCP, GDP etc., service providers.
Lead the development, implementation, and continuous improvement of the supplier qualification program, including risk-based classification, audit planning, and ongoing performance monitoring.
Conduct supplier audits (initial, routine, for-cause), prepare audit reports, track CAPAs, and verify implementation effectiveness.
Review and approve supplier quality documentation, such as Technical/Quality Agreements, audit responses, change notifications, and deviation reports.
Evaluate supplier quality systems and compliance with applicable international regulatory requirements (e.g., EMA, OECD GLP, VICH GCP, ISO/IEC 17025, HACCP, etc.).
Provide QA input into procurement decisions and cross-functional sourcing teams to ensure GxP compliance is considered in supplier selection.
Support internal stakeholders (e.g., R&amp;amp;D, Manufacturing, QC, Regulatory Affairs, Procurement) in supplier-related investigations and risk assessments.
Develop and deliver internal training on supplier qualification procedures and regulatory expectations.
Represent QA in cross-functional teams involving outsourced activities, ensuring the integrity of GxP-related data and deliverables.
Maintain accurate and current records in eQMS systems and supplier management databases.

 
What you need to apply:

Bachelor’s degree or higher in Life Sciences, Pharmacy, Biotechnology, or a related scientific discipline.
Minimum of 7–10 years of QA experience in the pharmaceutical, biologics, or veterinary vaccine industry.
At least 5 years of hands-on experience in GxP supplier qualification and auditing, with demonstrated expertise in GMP and at least one of the following: GLP, GCP, GDP.
Experience with laboratory testing, contract manufacturing, and/or clinical service providers preferred.
Proficiency in English (written and oral); additional languages are an asset.
Solid knowledge of EU GMP, FDA regulations, OECD GLP, VICH GCP, and ICH guidelines.
Proven ability to plan, conduct, and report external audits independently.
Strong understanding of quality systems, technical agreements, and risk-based approaches to supplier qualification.
Experience with quality investigations, CAPA management, and change control.
Proficiency with QMS tools, audit tracking systems, and MS Office; experience with eQMS platforms preferred.
Critical thinking, strong attention to detail, and ability to interpret complex regulations into operational requirements.
Excellent communication and interpersonal skills; capable of engaging with diverse stakeholders globally.
Willingness to travel domestically and internationally up to 25%

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Project Engineer (Senior) ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-12 11:35:00]]></date><referencenumber><![CDATA[1653]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1653&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer (Senior)  for our client based in Dublin. This role will require the candidate to support manufacturing at various aseptic drug product contract manufacturing sites around Europe. Assignments may include support for new product introductions, lifecycle changes and ongoing commercial production
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

 Develop as a drug product technical expert, to provide leadership and solutions troubleshooting parenteral drug product manufacturing, for all processing stages from drug substance thawing, formulation, filling, lyophilisation, inspection, and transportation of vials, syringes and devices for parenteral products through the new product introduction (NPI) or commercial phases.
Work with contract manufacturing partner SME’s, Global Operations, Contract Manufacturing Quality and drug product process teams.
Work as a member of cross site teams to support contract manufacturers and to identify and resolve potential issues
Provide process development expertise for commercial drug product processing in specific areas such as aseptic processing, process characterisation, technology transfer, and process validation.
Troubleshoot issues with drug product processing technologies and equipment.
Identify and implement operational improvements for current and new sterile operations.
Support commercial drug product manufacturing operations and contract manufacturing quality with technical evaluation of NC/CAPA.
Visit contract manufacturing sites to observe production operations and build relationships

 
What you need to apply:

3 -5 years' pharmaceutical manufacturing experience in either a drug product or drug substance manufacturing environment
Masters or PhD in a Science or Engineering or related discipline
Experience with aseptic drug product processes such as; component preparation (siliconization, autoclaving, depyrogenation), sterile filtration, filter integrity testing, filling, freeze drying, capping, manual and automated visual inspection
Experience with different aseptic drug product presentations such as pre-filled syringes, cartridges, lyophilised vials and liquid vials
Experience with the quality testing methods and interpretation of results for biological molecules
Aseptic drug product validation experience such as; media fill, sterilisation validation, equipment qualification, process validation
Experience dealing with contract manufacturing organisations

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Microbiology Medical Scientist – Part Time]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-22 14:14:30]]></date><referencenumber><![CDATA[1659]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1659&amp;Itemid=986]]></url><city><![CDATA[Limerick]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Microbiology Medical Scientist for our client based in Limerick. This is a part time position. he Microbiology Medical Scientist will play a critical role in supporting the daily operations of microbiology laboratory, ensuring a safe, compliant, and efficient working environment.
This hands-on, lab-based position involves maintaining laboratory safety standards, preparing microbial cultures and reagents, performing microbiological tests, and supporting non-scientific staff in handling live organisms.
The scientist is also responsible for operating and maintaining lab equipment, managing inventory and supplies, conducting routine safety checks, and maintaining detailed records to uphold GLP and biosafety protocols. Collaboration with EHS, Facilities, and cross-functional teams is essential to ensure consistent adherence to health, safety, and quality standards.
 
 
Why you should apply:

Join inspiring leaders and passionate colleagues committed to creating an inclusive, growth-focused, and rewarding workplace culture.
Enjoy outstanding career development and progression opportunities.
Highly competitive salary along with an excellent benefits package.

 
 
What you will be doing:

Supporting the safe and efficient operation of BD’s microbiology laboratory and ensuring adherence to all requisite health, safety, and quality standards at all times during the operation of these laboratories.
To write, maintain and enforce procedures relating to all areas of the microbiology laboratory and its related testing equipment.
To assist in training a team of non-scientific staff and facilitate arrangements to introduce professional visitors to the laboratory.
To operate and maintain laboratory equipment and perform microbiological testing to aid the non-scientific/ software associates
To support and contribute to effective execution of audit activities.
To assist in identifying and implementing operational procedures up to “best practice” standard in order to optimise use of resources.
To co-operate with the relevant staff in developing and leading the introduction of new ideas and technologies
Maintain inventory logs, monitor and restock lab supplies
Ensure adherence to all codes of and guidelines relating to professional practice and including the maintenance of Quality Assurance standards.
Conduct routine safety checks and walkthroughs to adhere to biosafety regulations.

 
What you need to apply:

Be registered on the Medical Scientists Register - Maintened by the Medical Scientists Registration Board at CORU 
Possess the fellowship or be eligible for fellowship of the Academy of Medical Laboratory Science (FAMLS) or equivalent. 
Posses membership or be eligible for membershipof the Academy of Medical Laboratory Science (MAMLS) or equivalent.
Experience in a Hospital Laboratory Microbiology Setting  2+ years of Satisfactory post-qualification experience. 
Excellent communication skills including the ability to present information in a clear and concise manner  Demonstrate effective team and interpersonal skills 
Excellent planning and organising skills  Demonstrate up-to-date knowledge of best practice in delivering a quality laboratory service and awareness of the requirements of ISO 15189 
Demonstrate up-to-date knowledge of antimicrobial susceptibility testing and guidelines 
Be familiar with laboratory information systems

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Sr Project Manager (Senior) - Process Development]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-01 10:21:22]]></date><referencenumber><![CDATA[1666]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1666&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Sr Project Manager (Senior) for our client based in Dublin. The Snr Project Manager – Process Development will report to the Sr. Manager Process Development in the Portfolio Management and Delivery (PMD) group and will be responsible for managing new product introduction and lifecycle management projects for drug product (DP) and finished drug products (FDP).
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Arrange agreement among the project team, customers, and management on the goals of the project
Develops and maintains the Project schedule/plan that addresses quality, objective, scope, cost, schedule, resources, and responsibilities - to deliver the project, and measure progress against schedule and budget
Effectively communicate with everyone involved in the project
Have a controlled scope in place, that is understood by all stakeholders and maintained throughout completion of the project
Execute prudent risk and issue management.
Maintains Actions/Risk and Decision logs
Generates and owns the GMP change control.
Motivate, support and direct project team members to deliver on project plan.
Leads Team meetings and cross functional collaboration
Works with resource managers from across the organisation to effectively obtain and allocate resources to complete programs and projects on time

 
What you need to apply:

Technical Degree and/or Masters’ or equivalent
5-8 years of experience (including min of 3yrs as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment
Preferred Experience: Portfolio Management, Portfolio Resource Management, Business Case Development  
Smartsheet, MS Office, MS Project, MS PowerPoint and MS Visio,
Trackwise Change Control &amp;amp; Document Management Systems
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[QC Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-13 12:14:01]]></date><referencenumber><![CDATA[1673]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1673&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QC Manager  for our client based in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
Conduct and supervise all aspects of API and OSD analytical testing.
Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
Participate in internal and external audits and address audit findings.
Prepare technical reports, lead investigations, and implement CAPAs.
Provide training and support to lab team to achieve daily and long-term goals.
Present technical data to stakeholders to facilitate prompt decision-making.
Report to the Senior QC Manager.

 
What you need to apply:

M.Sc./B.Sc. in Chemistry or a related discipline.
Minimum 4 years of experience in people management within a pharmaceutical lab setting.
Strong knowledge of QA/QC operations, analytical testing for API and OSD.
Excellent presentation and technical report writing skills.
Strong communication and interpersonal skills, with a commitment to quality and compliance.

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Management, Laboratory/Scientific]]></category></job><job><title><![CDATA[QA Validation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-14 11:32:45]]></date><referencenumber><![CDATA[1675]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1675&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Validation Engineer to join our Clients Quality team and take the lead in ensuring the site validation program meets global regulatory and compliance standards.   You’ll coordinate and execute validation activities for equipment, utilities, processes, and software—ensuring full compliance with FDA, EU cGMP, and GAMP standards. You’ll also support broader QA initiatives and drive continuous improvement across the site.
 
 
Why you should apply:

Work on high-impact projects, grow your career, and be part of a global team dedicated to quality, safety, and innovation.

 
What you will be doing:

Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance/execution of the Site Validation Master Plan.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards.
Generation of validation investigations and implementation of corrective actions
Creation/Review/Approval of various quality documents and test data.
Management of validation, exception event, and change control processes. Maintenance and tracking of validation equipment, if applicable.
Completing all required training before executing a task.
Documenting all activities in line with cGMP requirements.
Updating of validation procedures, job instructions and batch documentation to reflect current best practices.
Performing cross training within the team and training of new team members.
Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team members.
Maintaining the overall cGMP compliance of the production areas.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Qualification and/or degree in engineering or scientific discipline.
3 years plus validation/Quality experience.
3 years plus of knowledge of cGMP and regulatory requirements relating to the medical device industry.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[QA Validation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-14 11:32:45]]></date><referencenumber><![CDATA[1675-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1675&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Validation Engineer to join our Clients Quality team and take the lead in ensuring the site validation program meets global regulatory and compliance standards.   You’ll coordinate and execute validation activities for equipment, utilities, processes, and software—ensuring full compliance with FDA, EU cGMP, and GAMP standards. You’ll also support broader QA initiatives and drive continuous improvement across the site.
 
 
Why you should apply:

Work on high-impact projects, grow your career, and be part of a global team dedicated to quality, safety, and innovation.

 
What you will be doing:

Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance/execution of the Site Validation Master Plan.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards.
Generation of validation investigations and implementation of corrective actions
Creation/Review/Approval of various quality documents and test data.
Management of validation, exception event, and change control processes. Maintenance and tracking of validation equipment, if applicable.
Completing all required training before executing a task.
Documenting all activities in line with cGMP requirements.
Updating of validation procedures, job instructions and batch documentation to reflect current best practices.
Performing cross training within the team and training of new team members.
Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team members.
Maintaining the overall cGMP compliance of the production areas.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Qualification and/or degree in engineering or scientific discipline.
3 years plus validation/Quality experience.
3 years plus of knowledge of cGMP and regulatory requirements relating to the medical device industry.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[QA Validation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-14 11:32:45]]></date><referencenumber><![CDATA[1675-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1675&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Validation Engineer to join our Clients Quality team and take the lead in ensuring the site validation program meets global regulatory and compliance standards.   You’ll coordinate and execute validation activities for equipment, utilities, processes, and software—ensuring full compliance with FDA, EU cGMP, and GAMP standards. You’ll also support broader QA initiatives and drive continuous improvement across the site.
 
 
Why you should apply:

Work on high-impact projects, grow your career, and be part of a global team dedicated to quality, safety, and innovation.

 
What you will be doing:

Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance/execution of the Site Validation Master Plan.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards.
Generation of validation investigations and implementation of corrective actions
Creation/Review/Approval of various quality documents and test data.
Management of validation, exception event, and change control processes. Maintenance and tracking of validation equipment, if applicable.
Completing all required training before executing a task.
Documenting all activities in line with cGMP requirements.
Updating of validation procedures, job instructions and batch documentation to reflect current best practices.
Performing cross training within the team and training of new team members.
Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team members.
Maintaining the overall cGMP compliance of the production areas.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Qualification and/or degree in engineering or scientific discipline.
3 years plus validation/Quality experience.
3 years plus of knowledge of cGMP and regulatory requirements relating to the medical device industry.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[QA Validation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-14 11:32:45]]></date><referencenumber><![CDATA[1675-4]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1675&amp;Itemid=986]]></url><city><![CDATA[Leitrim]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Validation Engineer to join our Clients Quality team and take the lead in ensuring the site validation program meets global regulatory and compliance standards.   You’ll coordinate and execute validation activities for equipment, utilities, processes, and software—ensuring full compliance with FDA, EU cGMP, and GAMP standards. You’ll also support broader QA initiatives and drive continuous improvement across the site.
 
 
Why you should apply:

Work on high-impact projects, grow your career, and be part of a global team dedicated to quality, safety, and innovation.

 
What you will be doing:

Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance/execution of the Site Validation Master Plan.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards.
Generation of validation investigations and implementation of corrective actions
Creation/Review/Approval of various quality documents and test data.
Management of validation, exception event, and change control processes. Maintenance and tracking of validation equipment, if applicable.
Completing all required training before executing a task.
Documenting all activities in line with cGMP requirements.
Updating of validation procedures, job instructions and batch documentation to reflect current best practices.
Performing cross training within the team and training of new team members.
Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team members.
Maintaining the overall cGMP compliance of the production areas.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Qualification and/or degree in engineering or scientific discipline.
3 years plus validation/Quality experience.
3 years plus of knowledge of cGMP and regulatory requirements relating to the medical device industry.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[QA Validation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-14 11:32:45]]></date><referencenumber><![CDATA[1675-5]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1675&amp;Itemid=986]]></url><city><![CDATA[Donegal]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Validation Engineer to join our Clients Quality team and take the lead in ensuring the site validation program meets global regulatory and compliance standards.   You’ll coordinate and execute validation activities for equipment, utilities, processes, and software—ensuring full compliance with FDA, EU cGMP, and GAMP standards. You’ll also support broader QA initiatives and drive continuous improvement across the site.
 
 
Why you should apply:

Work on high-impact projects, grow your career, and be part of a global team dedicated to quality, safety, and innovation.

 
What you will be doing:

Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance/execution of the Site Validation Master Plan.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards.
Generation of validation investigations and implementation of corrective actions
Creation/Review/Approval of various quality documents and test data.
Management of validation, exception event, and change control processes. Maintenance and tracking of validation equipment, if applicable.
Completing all required training before executing a task.
Documenting all activities in line with cGMP requirements.
Updating of validation procedures, job instructions and batch documentation to reflect current best practices.
Performing cross training within the team and training of new team members.
Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team members.
Maintaining the overall cGMP compliance of the production areas.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Qualification and/or degree in engineering or scientific discipline.
3 years plus validation/Quality experience.
3 years plus of knowledge of cGMP and regulatory requirements relating to the medical device industry.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Automation Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-29 10:31:51]]></date><referencenumber><![CDATA[1681]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1681&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Automation Engineer (NPI)
Team Horizon is seeking a Automation Engineer (NPI) for a client in Mayo to provide technical support and program management to all manufacturing operations and NPI’s.
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Provide technical support to all control system related issues. Tasks include, daily trouble shooting, optimisation, and documentation control.
Leadership of control system qualification activities during project start-up.
Life cycle management of the onsite control systems, to GAMP-5 requirements.
Project management of control system elements of continuous improvement projects. Work closely with process engineers/ technical support chemists and other departments to deliver these continuous improvement projects.
Project management and technical development of future integrations of the control systems, with planned MES and ERP systems.
Adheres to and supports all EHS &amp;amp; E standards, procedures and policies.
Define proposals for long term plans for control system maintenance and improvements for management.
Comply with the EHS policy and procedures and demonstrate EHS best practices in all work activities

 What you need to apply:

B.Sc or B. Eng Degree or Post Graduate Diploma in a relevant technical discipline.(Masters desirable) Technical/Business Knowledge
 • 3+ years experience in process automation, with relevant experience of Vendor Packaged Equipment in a GMP environment in the pharmaceutical industry.
3 years experience of the 21 CFR Part 11 and EU Annex 11 requirements for automated systems in the pharmaceutical industry.
3 years plus experience of plant start-ups and/or new product introductions to GMP facilities. Must be able to lead these activities in a start-up environment.
Strong knowledge and experience of configuring and troubleshooting complex equipment control systems including PLC systems, and SCADA/HMI applications.
Knowledge and experience control system networks, e.g. Profinet, Profibus, Modbus or CANBus.
Knowledge and experience of Ethernet based networks, and network architecture models.
Knowledge and experience of interfacing systems with plant historians such as Ignition &amp;amp; OSI-PI using OPC interfaces.
Knowledge and experience of the life cycle management of control systems, including backup, recovery, user access controls, configuration management and change management.
Knowledge and experience of Windows operating system administration.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-03 10:45:07]]></date><referencenumber><![CDATA[1684]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1684&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Manager to lead the QA function at our clients manufacturing facility in Connaught. This position is responsible for ensuring that all products manufactured on site meet GMP requirements, regulatory expectations, and end-user standards, and will oversee team performance, manage compliance activities, and play a key role in preparing for and supporting audits and inspections.
 
 
Why you should apply:

This role offers the chance to lead a talented QA team within a highly regulated, dynamic, and collaborative environment, while playing a key role in ensuring that all products meet the highest standards of GMP, regulatory, and  quality requirements.
A great opportunity for someone who thrives in a leadership role, enjoys influencing quality strategy, and is passionate about driving continuous improvemenT

 
What you will be doing:

Ensure products manufactured meet requirements of end users, Regulatory Authorities, and company standards.
Lead and manage the Quality Assurance team, providing guidance and support on quality and compliance matters.
Act as a site contact for regulatory and customer audits/inspections (FDA, HPRA, etc.) and prepare site teams for successful outcomes.
Manage CAPA (Corrective and Preventive Action) implementation, and follow-up activities.
Collaborate cross-functionally to resolve quality issues, improve processes, and ensure continuous compliance with cGMP and other relevant regulations.
Promote department goals by attracting, developing, and retaining capable QA staff.
Contribute to talent management and professional development of QA personnel.  Develop, review, and approve QA documentation as related to general QA activities.
Provide oversight of batch record review, deviation investigations, change controls, and product release decisions.
Support quality meetings and key quality metrics and trends.
Communicate effectively with internal and external stakeholders, including the Quality and Compliance Group and regulatory bodies.
Serve as a designee for the Quality Director as required

 
What you need to apply:

Bachelor's degree in science, Quality, Engineering, or related field (
Minimum of 8 years’ experience in the healthcare, pharmaceutical, or biopharmaceutical industry 
At least 3 years’ supervisory/people management experience 
Demonstrated experience with audits and/or inspections (FDA, HPRA, etc.) 
High level of expertise in day-to-day quality and compliance decision-making In-depth knowledge of GMP requirements and regulatory frameworks 
Strong attention to detail and commitment to compliance and quality standards 
Ability to facilitate quality decision-making while maintaining a strong patient focus and upholding company reputation

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management]]></category></job><job><title><![CDATA[QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-03 10:45:07]]></date><referencenumber><![CDATA[1684-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1684&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Manager to lead the QA function at our clients manufacturing facility in Connaught. This position is responsible for ensuring that all products manufactured on site meet GMP requirements, regulatory expectations, and end-user standards, and will oversee team performance, manage compliance activities, and play a key role in preparing for and supporting audits and inspections.
 
 
Why you should apply:

This role offers the chance to lead a talented QA team within a highly regulated, dynamic, and collaborative environment, while playing a key role in ensuring that all products meet the highest standards of GMP, regulatory, and  quality requirements.
A great opportunity for someone who thrives in a leadership role, enjoys influencing quality strategy, and is passionate about driving continuous improvemenT

 
What you will be doing:

Ensure products manufactured meet requirements of end users, Regulatory Authorities, and company standards.
Lead and manage the Quality Assurance team, providing guidance and support on quality and compliance matters.
Act as a site contact for regulatory and customer audits/inspections (FDA, HPRA, etc.) and prepare site teams for successful outcomes.
Manage CAPA (Corrective and Preventive Action) implementation, and follow-up activities.
Collaborate cross-functionally to resolve quality issues, improve processes, and ensure continuous compliance with cGMP and other relevant regulations.
Promote department goals by attracting, developing, and retaining capable QA staff.
Contribute to talent management and professional development of QA personnel.  Develop, review, and approve QA documentation as related to general QA activities.
Provide oversight of batch record review, deviation investigations, change controls, and product release decisions.
Support quality meetings and key quality metrics and trends.
Communicate effectively with internal and external stakeholders, including the Quality and Compliance Group and regulatory bodies.
Serve as a designee for the Quality Director as required

 
What you need to apply:

Bachelor's degree in science, Quality, Engineering, or related field (
Minimum of 8 years’ experience in the healthcare, pharmaceutical, or biopharmaceutical industry 
At least 3 years’ supervisory/people management experience 
Demonstrated experience with audits and/or inspections (FDA, HPRA, etc.) 
High level of expertise in day-to-day quality and compliance decision-making In-depth knowledge of GMP requirements and regulatory frameworks 
Strong attention to detail and commitment to compliance and quality standards 
Ability to facilitate quality decision-making while maintaining a strong patient focus and upholding company reputation

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management]]></category></job><job><title><![CDATA[QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-03 10:45:07]]></date><referencenumber><![CDATA[1684-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1684&amp;Itemid=986]]></url><city><![CDATA[Leitrim]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Manager to lead the QA function at our clients manufacturing facility in Connaught. This position is responsible for ensuring that all products manufactured on site meet GMP requirements, regulatory expectations, and end-user standards, and will oversee team performance, manage compliance activities, and play a key role in preparing for and supporting audits and inspections.
 
 
Why you should apply:

This role offers the chance to lead a talented QA team within a highly regulated, dynamic, and collaborative environment, while playing a key role in ensuring that all products meet the highest standards of GMP, regulatory, and  quality requirements.
A great opportunity for someone who thrives in a leadership role, enjoys influencing quality strategy, and is passionate about driving continuous improvemenT

 
What you will be doing:

Ensure products manufactured meet requirements of end users, Regulatory Authorities, and company standards.
Lead and manage the Quality Assurance team, providing guidance and support on quality and compliance matters.
Act as a site contact for regulatory and customer audits/inspections (FDA, HPRA, etc.) and prepare site teams for successful outcomes.
Manage CAPA (Corrective and Preventive Action) implementation, and follow-up activities.
Collaborate cross-functionally to resolve quality issues, improve processes, and ensure continuous compliance with cGMP and other relevant regulations.
Promote department goals by attracting, developing, and retaining capable QA staff.
Contribute to talent management and professional development of QA personnel.  Develop, review, and approve QA documentation as related to general QA activities.
Provide oversight of batch record review, deviation investigations, change controls, and product release decisions.
Support quality meetings and key quality metrics and trends.
Communicate effectively with internal and external stakeholders, including the Quality and Compliance Group and regulatory bodies.
Serve as a designee for the Quality Director as required

 
What you need to apply:

Bachelor's degree in science, Quality, Engineering, or related field (
Minimum of 8 years’ experience in the healthcare, pharmaceutical, or biopharmaceutical industry 
At least 3 years’ supervisory/people management experience 
Demonstrated experience with audits and/or inspections (FDA, HPRA, etc.) 
High level of expertise in day-to-day quality and compliance decision-making In-depth knowledge of GMP requirements and regulatory frameworks 
Strong attention to detail and commitment to compliance and quality standards 
Ability to facilitate quality decision-making while maintaining a strong patient focus and upholding company reputation

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management]]></category></job><job><title><![CDATA[QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-03 10:45:07]]></date><referencenumber><![CDATA[1684-4]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1684&amp;Itemid=986]]></url><city><![CDATA[Donegal]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Manager to lead the QA function at our clients manufacturing facility in Connaught. This position is responsible for ensuring that all products manufactured on site meet GMP requirements, regulatory expectations, and end-user standards, and will oversee team performance, manage compliance activities, and play a key role in preparing for and supporting audits and inspections.
 
 
Why you should apply:

This role offers the chance to lead a talented QA team within a highly regulated, dynamic, and collaborative environment, while playing a key role in ensuring that all products meet the highest standards of GMP, regulatory, and  quality requirements.
A great opportunity for someone who thrives in a leadership role, enjoys influencing quality strategy, and is passionate about driving continuous improvemenT

 
What you will be doing:

Ensure products manufactured meet requirements of end users, Regulatory Authorities, and company standards.
Lead and manage the Quality Assurance team, providing guidance and support on quality and compliance matters.
Act as a site contact for regulatory and customer audits/inspections (FDA, HPRA, etc.) and prepare site teams for successful outcomes.
Manage CAPA (Corrective and Preventive Action) implementation, and follow-up activities.
Collaborate cross-functionally to resolve quality issues, improve processes, and ensure continuous compliance with cGMP and other relevant regulations.
Promote department goals by attracting, developing, and retaining capable QA staff.
Contribute to talent management and professional development of QA personnel.  Develop, review, and approve QA documentation as related to general QA activities.
Provide oversight of batch record review, deviation investigations, change controls, and product release decisions.
Support quality meetings and key quality metrics and trends.
Communicate effectively with internal and external stakeholders, including the Quality and Compliance Group and regulatory bodies.
Serve as a designee for the Quality Director as required

 
What you need to apply:

Bachelor's degree in science, Quality, Engineering, or related field (
Minimum of 8 years’ experience in the healthcare, pharmaceutical, or biopharmaceutical industry 
At least 3 years’ supervisory/people management experience 
Demonstrated experience with audits and/or inspections (FDA, HPRA, etc.) 
High level of expertise in day-to-day quality and compliance decision-making In-depth knowledge of GMP requirements and regulatory frameworks 
Strong attention to detail and commitment to compliance and quality standards 
Ability to facilitate quality decision-making while maintaining a strong patient focus and upholding company reputation

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management]]></category></job><job><title><![CDATA[Automation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-05 14:17:48]]></date><referencenumber><![CDATA[1688]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1688&amp;Itemid=986]]></url><city><![CDATA[Remote]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Automation Engineer  
Team Horizon is seeking an Automation Engineer for a client in the pharmaceutical industry who has proven expertise in Ignition SCADA and hands-on experience using Ignition SCADA across multiple pharmaceutical projects.
The successful candidate will play a key role in deploying, configuring, and supporting Ignition SCADA systems across various global manufacturing sites, while working collaboratively to improve operational efficiency and compliance.
 Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives
Fully remote role with occasional travel to sites in Ireland.

 What you will be doing:

Lead and support the deployment of Ignition SCADA solutions across multiple sites within the organization.
Maintain, standardize, and optimize global use case templates for consistent SCADA deployment.
Roll out global templates, ensuring uniformity and best practices across all deployments.
Collaborate closely with IT and engineering teams to develop interfaces between Ignition and various enterprise-level systems (ERP/MES/LIMS/etc.).
Develop, update, and enforce engineering standards and procedures related to automation and SCADA implementations.
Troubleshoot, maintain, and optimize Ignition SCADA systems for maximum uptime and performance.
Train and support local engineering/operations personnel on Ignition system best practices.

 What you need to apply:

Bachelor’s degree in Engineering, Computer Science, or a related field.
3-5 years experience working on pharmaceutical automation projects, with expert hands-on knowledge of Ignition SCADA.
Understanding of regulatory requirements (GMP, FDA, etc.) within the pharmaceutical industry.
Proven track record of deploying SCADA solutions globally and maintaining standard templates or design assets.
Experience delivering interfaces between SCADA and enterprise platforms (such as ERP, MES, SQL databases).
Strong communication and collaboration skills to work effectively with cross-functional teams.
Knowledge of engineering documentation standards and ability to author procedures.
]]></description><jobtype><![CDATA[Remote, Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Sr Project Manager (Senior) ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-18 09:40:47]]></date><referencenumber><![CDATA[1696]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1696&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[ 
Team Horizon is seeking a Sr Project Manager (Senior) for our client based in Dublin (Hybrid). The Senior Project Manager — Manufacturing Support is responsible for a broad variety of project management activities that support both Direct Manufacturing and Manufacturing Support across vial and syringe drug-product (DP) and finished drug-product (FDP) operations.
The role will help plan, coordinate and deliver New Product Introductions (NPIs), deviation lifecycle development, operational and strategic projects (including capital, reliability and process-improvement / volume initiatives). Embedded in Manufacturing Support, the post will partner closely with Direct Manufacturing, Process &amp;amp; Aseptic Owners, Quality, Engineering, Validation, MES/, Technical Writing and other site and global stakeholders to establish safe, compliant and sustainable project management that maintain supply continuity.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Support both Direct Manufacturing and Manufacturing Support across vial and syringe drug-product (DP) and finished drug-product (FDP) operations.
Project manage timelines associated with complex investigations (deviations, aseptic excursions, batch issues, equipment failures) owning timelines, meeting scheduling, communications and lifecycle visualisations / tracking.
Maintain daily/weekly project momentum with clear project controls, ensuring on-site presence and hands-on leadership of cross-functional teams.
Lead and facilitate project meetings and governance forums to accurately capture and nd track actions, timelines, deliverables, milestones and decision-points; clarify and document roles and responsibilities and ensure timely closure and verification of action owners’ commitments.
Provide timely escalation of project risks and issues and make decisions that enable progress within the contract timeline.
Effectively communicate with everyone involved in the project
Have a controlled scope in place, that is understood by all stakeholders maintained throughout completion of the project
Maintains Actions/Risk and Decision logs
Works with resource managers from across the organisation to effectively obtain and allocate resources to complete programs and projects on timeScope of role
Define and align project objectives with Direct Manufacturing customers and site leadership. Create and maintain comprehensive project plans that address quality, scope, cost, schedule, resources and manufacturing readiness.
Project Manage medium to large technical projects (capital, reliability, NPI, lifecycle) from concept through design reviews, build, validation readiness and handover to operations.  

 
 
 
What you need to apply:

Technical Degree and/or Masters’ or equivalent 
5-8 years of experience (including min of 3yrs as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment 
Portfolio Management, Portfolio Resource Management, Business Case Development    
PMP or PRINCE2 certification. 
Experience with Lean Six Sigma methodologies. 
Knowledge of industry-specific regulations and standards.    
Smartsheet, MS Office, MS Project, MS PowerPoint and MS Visio, 
Trackwise Change Control &amp;amp; Document Management Systems

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Operations Shift Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-24 17:29:13]]></date><referencenumber><![CDATA[1699]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1699&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Operations Shift Manager for our client based in Mayo.
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Mayo

 
What you will be doing:

Manage, lead and motivate a multi-skilled Operations group in an empowered team-based environment, ensuring full engagement of team members.
Ensure daily operations are carried out in compliance with all appropriate safety, quality and environmental standards.
Execute daily and weekly production plans to meet all Business Plan commitments.
Ensure timely completion of all corrective and preventive actions to avoid repeats of Service and Quality defects, and all audit non-conformances.
Ensure a consistently high level of communication with the Operations team members through daily, weekly, and monthly routines.
Drive, manage and embed operational excellence and a continuous improvement culture within the team to deliver improvements through lean principles and systems.

 
What you need to apply:

Third level qualification, diploma or degree in a business or technical discipline required.
A minimum of 5 years’ experience in a high-volume manufacturing environment.
Demonstrated experience in people management in a people focused, team-based environment.
Excellent analytical, problem solving and decision-making skills.
Excellent communication and interpersonal skills.
Comfortable working in a team based, matrixed, ambiguous environment.
Ability to manage multiple conflicting demands and to prioritize accordingly.
High level of PC literacy. 
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Senior Software Quality Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-25 16:51:27]]></date><referencenumber><![CDATA[1700]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1700&amp;Itemid=986]]></url><city><![CDATA[Limerick]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Software Quality Engineer for a global medical technology company.
 
 
Why you should apply:

Learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. 

 
 
What you will be doing:

Develop, enhance and maintain strategies and plans to improve the overall quality of software, including test coverage and system performance.
Provides strategic and tactical support of the Quality Engineering Function, based on an understanding of 21 CFR Part 820 and ISO Requirements.
Owns and facilitates the Design Review and Functional Review Process for software products.
Collaborates with Manufacturing and R&amp;amp;D to support software products, driving design improvements and monitoring measurable enhancements. Routinely interacts with multifunctional groups.
Ensures  PI Systems divisional, departmental policies, procedures, practices, and facilities are in compliance with all applicable regulatory guidelines.
Represent the Quality Function for New Product Development Core Teams and/or Technology Transfer Core Team
Plays a key role as a core team member in software development projects, handling various tasks such as requirements, SW development planning, risk management, V&amp;amp;V, and other work.
Remediates software-related audit findings and CAPAs.

 
What you need to apply:

Bachelor’s degree in Electrical, Mechanical, Software or Biomedical Engineering or other relevant technical area with 6 to 7 years of experience, where 4 of those years are progressive experience in software development or lifecycle management.
Or MS/MBA with 7 years of experience, where 5 of those years are progressive experience in software development or lifecycle management. 
Ability and skill to effectively manage multiple tasks and lead execution of change management plans
Ability and skill to handle the Quality function for design projects, reliability concepts for complex systems, validation planning and statistical sampling, Six Sigma root cause analysis tools and project management techniques 
Ability to effectively write communications that ensure clarity, accuracy and consideration of the audience 
Ability to speak with clarity and express points of view in a variety of settings: one-on-one interactions, group meetings, and formal presentations 
Ability to listen to others, including associates, managers, peers and customers, when making decisions and solving problems 
Ability and skill to analyse using systematic analysis tools that include root cause, failure analysis and risk assessment to gather critical information and diagnose 
Ability to drive for results and effectively work through conflicts in working teams by facilitating conflict resolution 
Working knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO).

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, IT/Software]]></category></job><job><title><![CDATA[Validation Engineer - Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-02 09:36:37]]></date><referencenumber><![CDATA[1702]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1702&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Validation Engineer for our Clients manufacturing facility in Connaught on a 6-month initial contract. You will coordinate, implement, and actively contribute to the site’s Validation Program—ensuring full compliance with regulatory, data integrity, and company requirements.
 
 
Why you should apply:

This is a high-impact role with autonomy and visibility across multiple functions.

 
What you will be doing:

Ensure all Computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements.
Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance of the Validation Master Plans.
Generation/maintenance of Project Validation Plans.
Generation of validation plans, protocols and final reports to cGMP standard.
Understanding of Risk based equipment qualification, Equipment Risk Assessments, Critical Elements Test Plan development
Review / approval of all protocols and final reports.
Management of validation change control process.
Adheres to and supports all EHS &amp;amp; E standards, procedures and policies

 
What you need to apply:

A minimum of 5-10 years’ experience in a cGMP regulated environment.
A good understanding of regulatory requirements.
Must have hands on experience of execution of IQ/OQ/PQ for Facilities/ Utilities/ Equipment in Pharmaceuticals or Medical Devices or Diagnostics 
Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
Requires proven problem-solving skills and the ability to adapt to new regulatory requirements.
Requires innovative thinking, where new and untested solutions are proposed, demonstrated and implemented on a regular basis.
Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders.
Requires total commitment to quality and maintaining a high standard of work at all times.
Demonstrates the highest levels of integrity and a strong work ethic at all times
Strong communication skills both verbal and written are required for the execution of this role.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineer - Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-02 09:36:37]]></date><referencenumber><![CDATA[1702-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1702&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Validation Engineer for our Clients manufacturing facility in Connaught on a 6-month initial contract. You will coordinate, implement, and actively contribute to the site’s Validation Program—ensuring full compliance with regulatory, data integrity, and company requirements.
 
 
Why you should apply:

This is a high-impact role with autonomy and visibility across multiple functions.

 
What you will be doing:

Ensure all Computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements.
Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance of the Validation Master Plans.
Generation/maintenance of Project Validation Plans.
Generation of validation plans, protocols and final reports to cGMP standard.
Understanding of Risk based equipment qualification, Equipment Risk Assessments, Critical Elements Test Plan development
Review / approval of all protocols and final reports.
Management of validation change control process.
Adheres to and supports all EHS &amp;amp; E standards, procedures and policies

 
What you need to apply:

A minimum of 5-10 years’ experience in a cGMP regulated environment.
A good understanding of regulatory requirements.
Must have hands on experience of execution of IQ/OQ/PQ for Facilities/ Utilities/ Equipment in Pharmaceuticals or Medical Devices or Diagnostics 
Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
Requires proven problem-solving skills and the ability to adapt to new regulatory requirements.
Requires innovative thinking, where new and untested solutions are proposed, demonstrated and implemented on a regular basis.
Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders.
Requires total commitment to quality and maintaining a high standard of work at all times.
Demonstrates the highest levels of integrity and a strong work ethic at all times
Strong communication skills both verbal and written are required for the execution of this role.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineer - Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-02 09:36:37]]></date><referencenumber><![CDATA[1702-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1702&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Validation Engineer for our Clients manufacturing facility in Connaught on a 6-month initial contract. You will coordinate, implement, and actively contribute to the site’s Validation Program—ensuring full compliance with regulatory, data integrity, and company requirements.
 
 
Why you should apply:

This is a high-impact role with autonomy and visibility across multiple functions.

 
What you will be doing:

Ensure all Computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements.
Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance of the Validation Master Plans.
Generation/maintenance of Project Validation Plans.
Generation of validation plans, protocols and final reports to cGMP standard.
Understanding of Risk based equipment qualification, Equipment Risk Assessments, Critical Elements Test Plan development
Review / approval of all protocols and final reports.
Management of validation change control process.
Adheres to and supports all EHS &amp;amp; E standards, procedures and policies

 
What you need to apply:

A minimum of 5-10 years’ experience in a cGMP regulated environment.
A good understanding of regulatory requirements.
Must have hands on experience of execution of IQ/OQ/PQ for Facilities/ Utilities/ Equipment in Pharmaceuticals or Medical Devices or Diagnostics 
Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
Requires proven problem-solving skills and the ability to adapt to new regulatory requirements.
Requires innovative thinking, where new and untested solutions are proposed, demonstrated and implemented on a regular basis.
Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders.
Requires total commitment to quality and maintaining a high standard of work at all times.
Demonstrates the highest levels of integrity and a strong work ethic at all times
Strong communication skills both verbal and written are required for the execution of this role.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineer - Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-02 09:36:37]]></date><referencenumber><![CDATA[1702-4]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1702&amp;Itemid=986]]></url><city><![CDATA[Leitrim]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Validation Engineer for our Clients manufacturing facility in Connaught on a 6-month initial contract. You will coordinate, implement, and actively contribute to the site’s Validation Program—ensuring full compliance with regulatory, data integrity, and company requirements.
 
 
Why you should apply:

This is a high-impact role with autonomy and visibility across multiple functions.

 
What you will be doing:

Ensure all Computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements.
Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance of the Validation Master Plans.
Generation/maintenance of Project Validation Plans.
Generation of validation plans, protocols and final reports to cGMP standard.
Understanding of Risk based equipment qualification, Equipment Risk Assessments, Critical Elements Test Plan development
Review / approval of all protocols and final reports.
Management of validation change control process.
Adheres to and supports all EHS &amp;amp; E standards, procedures and policies

 
What you need to apply:

A minimum of 5-10 years’ experience in a cGMP regulated environment.
A good understanding of regulatory requirements.
Must have hands on experience of execution of IQ/OQ/PQ for Facilities/ Utilities/ Equipment in Pharmaceuticals or Medical Devices or Diagnostics 
Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
Requires proven problem-solving skills and the ability to adapt to new regulatory requirements.
Requires innovative thinking, where new and untested solutions are proposed, demonstrated and implemented on a regular basis.
Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders.
Requires total commitment to quality and maintaining a high standard of work at all times.
Demonstrates the highest levels of integrity and a strong work ethic at all times
Strong communication skills both verbal and written are required for the execution of this role.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineer - Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-02 09:36:37]]></date><referencenumber><![CDATA[1702-5]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1702&amp;Itemid=986]]></url><city><![CDATA[Donegal]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Validation Engineer for our Clients manufacturing facility in Connaught on a 6-month initial contract. You will coordinate, implement, and actively contribute to the site’s Validation Program—ensuring full compliance with regulatory, data integrity, and company requirements.
 
 
Why you should apply:

This is a high-impact role with autonomy and visibility across multiple functions.

 
What you will be doing:

Ensure all Computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements.
Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generation/maintenance of the Validation Master Plans.
Generation/maintenance of Project Validation Plans.
Generation of validation plans, protocols and final reports to cGMP standard.
Understanding of Risk based equipment qualification, Equipment Risk Assessments, Critical Elements Test Plan development
Review / approval of all protocols and final reports.
Management of validation change control process.
Adheres to and supports all EHS &amp;amp; E standards, procedures and policies

 
What you need to apply:

A minimum of 5-10 years’ experience in a cGMP regulated environment.
A good understanding of regulatory requirements.
Must have hands on experience of execution of IQ/OQ/PQ for Facilities/ Utilities/ Equipment in Pharmaceuticals or Medical Devices or Diagnostics 
Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
Requires proven problem-solving skills and the ability to adapt to new regulatory requirements.
Requires innovative thinking, where new and untested solutions are proposed, demonstrated and implemented on a regular basis.
Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders.
Requires total commitment to quality and maintaining a high standard of work at all times.
Demonstrates the highest levels of integrity and a strong work ethic at all times
Strong communication skills both verbal and written are required for the execution of this role.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Sr Validation Engineer - Hybrid]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-18 11:45:58]]></date><referencenumber><![CDATA[1705]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1705&amp;Itemid=986]]></url><city><![CDATA[Dublin / Hybrid ]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Sr Validation Engineer for various capital and equipment lifecycle projects joining a dynamic team. This role will be responsible for equipment validation in Sterile Fill Finish to ensure the maximum levels of performance and compliance are maintained.
 
Why you should apply:

Direct ownership of end-to-end CQV activities across high-impact capital and equipment lifecycle projects.
Working within a dynamic, cross-functional team on complex, regulated systems also provides opportunity for excellent professional growth, visibility, and the chance to influence best-practice validation strategies in a critical manufacturing environment.

 
What you will be doing:

Ensure the activities are completed safely, as per schedule and in compliance with GMP and Quality Requirements.
Provide expert technical validation support to meet site objectives, comprising of the full validation lifecycles process from initial design through qualification to validation maintenance (eg. Periodic review)
Coordinates the qualification activities and maintain Equipment and utility systems in a validated state
Development or qualification approaches and equipment family strategies
Assist in the development of User Requirement Specifications (URS’s) and Quality Risk Assessment for Equipment and Automated Systems (QRAES)
Development and approval of C&amp;amp;Q / Validation Plans, FAT, SAT IV/FTs, QRAES, IOQ’s, PQ’s etc. for the Vial and Syringe filling, formulation, inspection and utility areas in line with GMP’s, regulatory requirements and corporate standards.
Ensures Startup of equipment/utilities is completed in a safe and coordinated manner. Ensures the safe startup of equipment and utilities.
Liaise with Engineering, Commissioning and Qualification, manufacturing, planning and PD and external vendors regarding equipment User Requirement Specifications, Factory Acceptance Tests to ensure the quality by design principles are being followed.
Assist in the development and improvements of the equipment validation lifecycle process while ensuring continued compliance to all necessary regulations.
Participate in regulatory inspections, regulatory filings and RTQ’s (response to questions).
Update and maintain Standard Operating Procedures (SOP's) in accordance with site and corporate requirements.
Take ownership for quality compliance in all activities you are responsible for, Ensuring approaches are aligned with current guidelines (ICH/ASTM)
Ensure the site change control procedure is adhered to.

 
What you need to apply:

6+ years experience in Science, Engineering or Validation, Commissioning and Qualification Management
Technical qualification at third level or equivalent in Engineering or science.
Extensive knowledge and demonstrated experience managing Commissioning and Qualification for Pharmaceutical / Biotechnology projects
Strong understanding of a risk-based approach to commissioning and qualification within the biotechnology industry
Experience of sterile / biotech equipment within the pharmaceutical industry is preferred.
Experience qualifying filling, formulation and utility systems within the sterile manufacturing environment of drug product.
Knowledge of safety, GMP and environmental regulatory requirements.
Participate, when required, as a member of a multidisciplinary site and multisite teams, e.g. Cross Functional Investigation Team or NPI regulatory marketing applications.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Sr Validation Engineer - Hybrid]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-18 11:45:58]]></date><referencenumber><![CDATA[1705-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1705&amp;Itemid=986]]></url><city><![CDATA[Dublin / Hybrid ]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Sr Validation Engineer for various capital and equipment lifecycle projects joining a dynamic team. This role will be responsible for equipment validation in Sterile Fill Finish to ensure the maximum levels of performance and compliance are maintained.
 
Why you should apply:

Direct ownership of end-to-end CQV activities across high-impact capital and equipment lifecycle projects.
Working within a dynamic, cross-functional team on complex, regulated systems also provides opportunity for excellent professional growth, visibility, and the chance to influence best-practice validation strategies in a critical manufacturing environment.

 
What you will be doing:

Ensure the activities are completed safely, as per schedule and in compliance with GMP and Quality Requirements.
Provide expert technical validation support to meet site objectives, comprising of the full validation lifecycles process from initial design through qualification to validation maintenance (eg. Periodic review)
Coordinates the qualification activities and maintain Equipment and utility systems in a validated state
Development or qualification approaches and equipment family strategies
Assist in the development of User Requirement Specifications (URS’s) and Quality Risk Assessment for Equipment and Automated Systems (QRAES)
Development and approval of C&amp;amp;Q / Validation Plans, FAT, SAT IV/FTs, QRAES, IOQ’s, PQ’s etc. for the Vial and Syringe filling, formulation, inspection and utility areas in line with GMP’s, regulatory requirements and corporate standards.
Ensures Startup of equipment/utilities is completed in a safe and coordinated manner. Ensures the safe startup of equipment and utilities.
Liaise with Engineering, Commissioning and Qualification, manufacturing, planning and PD and external vendors regarding equipment User Requirement Specifications, Factory Acceptance Tests to ensure the quality by design principles are being followed.
Assist in the development and improvements of the equipment validation lifecycle process while ensuring continued compliance to all necessary regulations.
Participate in regulatory inspections, regulatory filings and RTQ’s (response to questions).
Update and maintain Standard Operating Procedures (SOP's) in accordance with site and corporate requirements.
Take ownership for quality compliance in all activities you are responsible for, Ensuring approaches are aligned with current guidelines (ICH/ASTM)
Ensure the site change control procedure is adhered to.

 
What you need to apply:

6+ years experience in Science, Engineering or Validation, Commissioning and Qualification Management
Technical qualification at third level or equivalent in Engineering or science.
Extensive knowledge and demonstrated experience managing Commissioning and Qualification for Pharmaceutical / Biotechnology projects
Strong understanding of a risk-based approach to commissioning and qualification within the biotechnology industry
Experience of sterile / biotech equipment within the pharmaceutical industry is preferred.
Experience qualifying filling, formulation and utility systems within the sterile manufacturing environment of drug product.
Knowledge of safety, GMP and environmental regulatory requirements.
Participate, when required, as a member of a multidisciplinary site and multisite teams, e.g. Cross Functional Investigation Team or NPI regulatory marketing applications.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Sr Validation Engineer - Hybrid]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-18 11:45:58]]></date><referencenumber><![CDATA[1705-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1705&amp;Itemid=986]]></url><city><![CDATA[Dublin / Hybrid ]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Sr Validation Engineer for various capital and equipment lifecycle projects joining a dynamic team. This role will be responsible for equipment validation in Sterile Fill Finish to ensure the maximum levels of performance and compliance are maintained.
 
Why you should apply:

Direct ownership of end-to-end CQV activities across high-impact capital and equipment lifecycle projects.
Working within a dynamic, cross-functional team on complex, regulated systems also provides opportunity for excellent professional growth, visibility, and the chance to influence best-practice validation strategies in a critical manufacturing environment.

 
What you will be doing:

Ensure the activities are completed safely, as per schedule and in compliance with GMP and Quality Requirements.
Provide expert technical validation support to meet site objectives, comprising of the full validation lifecycles process from initial design through qualification to validation maintenance (eg. Periodic review)
Coordinates the qualification activities and maintain Equipment and utility systems in a validated state
Development or qualification approaches and equipment family strategies
Assist in the development of User Requirement Specifications (URS’s) and Quality Risk Assessment for Equipment and Automated Systems (QRAES)
Development and approval of C&amp;amp;Q / Validation Plans, FAT, SAT IV/FTs, QRAES, IOQ’s, PQ’s etc. for the Vial and Syringe filling, formulation, inspection and utility areas in line with GMP’s, regulatory requirements and corporate standards.
Ensures Startup of equipment/utilities is completed in a safe and coordinated manner. Ensures the safe startup of equipment and utilities.
Liaise with Engineering, Commissioning and Qualification, manufacturing, planning and PD and external vendors regarding equipment User Requirement Specifications, Factory Acceptance Tests to ensure the quality by design principles are being followed.
Assist in the development and improvements of the equipment validation lifecycle process while ensuring continued compliance to all necessary regulations.
Participate in regulatory inspections, regulatory filings and RTQ’s (response to questions).
Update and maintain Standard Operating Procedures (SOP's) in accordance with site and corporate requirements.
Take ownership for quality compliance in all activities you are responsible for, Ensuring approaches are aligned with current guidelines (ICH/ASTM)
Ensure the site change control procedure is adhered to.

 
What you need to apply:

6+ years experience in Science, Engineering or Validation, Commissioning and Qualification Management
Technical qualification at third level or equivalent in Engineering or science.
Extensive knowledge and demonstrated experience managing Commissioning and Qualification for Pharmaceutical / Biotechnology projects
Strong understanding of a risk-based approach to commissioning and qualification within the biotechnology industry
Experience of sterile / biotech equipment within the pharmaceutical industry is preferred.
Experience qualifying filling, formulation and utility systems within the sterile manufacturing environment of drug product.
Knowledge of safety, GMP and environmental regulatory requirements.
Participate, when required, as a member of a multidisciplinary site and multisite teams, e.g. Cross Functional Investigation Team or NPI regulatory marketing applications.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Quality Assurance Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-18 12:50:53]]></date><referencenumber><![CDATA[1706]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1706&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking an experienced Quality Assurance Specialist to play a key role in a high-impact project, providing QA oversight for operational readiness, validation, and technology transfer activities supporting the introduction of new component combinations and aseptic filling operations.
 
Why you should apply:

This role is an excellent opportunity because it places you in a influential QA position where your expertise directly shapes the quality and compliance of aseptic drug products that reach patients worldwide.
You’ll act as a key quality decision-maker for new product introductions, tech transfers, and process validation giving you real ownership, visibility, and impact across the, site.
 

What you will be doing:

This role will ensure quality and compliance across integrated line qualification, media fill execution, and product introduction activities, working closely with Engineering, Operations, and Process Development teams.
Operational Readiness, Validation &amp;amp; Documentation •          Provide QA leadership duringdesign of new rooms, development of materials/people/waste flows and contamination controls (gowning, cleaning, desinfection)ensuring operational robustness. QA review/approve associated risk assestments and SOP.  •          Review and approve validation documentation including integrated line PQs, media fills, and environmental monitoring qualifications. •          Support QA review of MBR and recipe creation for filling, lyophilisation, and associated aseptic operations. •          Ensure readiness of operational documentation including SOPs, batch records, and contamination control strategies. •          Contribute to the review of contamination control, isolator qualification (including smoke studies and VHP qualification), and environmental monitoring performance qualification (EMPQ). •          Maintain oversight of validation and readiness documentation to ensure it is audit-ready, scientifically sound, and compliant with standards and cGMP.
Technology Transfer &amp;amp; New Product Introduction (NPI) •          Serve as the QA Lead for technology transfer and NPI activities, providing quality oversight throughout process validation and product lifecycle introduction. •          Review and approve technology transfer documentation including process descriptions, PPQ protocols, validation reports, and risk assessments. •          Partner cross-functionally with Technical, Engineering, and Operations teams to ensure all NPI activities are compliant with regulatory and site quality requirements. •          Ensure alignment of transfer activities with global validation and quality system standards.
Quality Systems, Risk Management &amp;amp; Compliance •          Lead and support deviation, CAPA, and change control management related to operational readiness, validation, and tech transfer activities. •          Conduct quality risk assessments for new processes, interventions, and aseptic operations. •          Ensure data integrity and right-first-time execution across all readiness and validation deliverables. •          Support inspection readiness and regulatory audits, representing QA for validation and NPI areas

 
What you need to apply:

Bachelor’s or Master’s degree in Science, Engineering, Biotechnology, or related discipline.
Minimum 8 years’ experience in pharmaceutical or biotechnology manufacturing 
Proven expertise in facility startup and Quality Oversight of Operational Readiness and technology transfer activities.
In-depth knowledge of applicable regulatory requirements and experience with regulatory inspections including EU/FDA GMP, Annex 1, and process validation lifecycle requirements.       Experience working in aseptic operations, relating to vial and syringe filling.
Experience managing change control, deviations, and CAPAs through electronic QMS systems (e.g., TrackWise, Veeva Vault, PAS-X, SAP).

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Contract Development &amp; Mfg Mgr]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-06 10:32:49]]></date><referencenumber><![CDATA[1711]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1711&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Contract Development &amp;amp; Mfg Mgr for our client based in Dublin. This is a hybrid position. They are seeking an external contract worker to join the External Process Development Organization initially for a 12 month period . The Contract Testing Laboratory (CTL) will work with CRO’s/CTLs’s to deliver on pipeline molecules. The CTL team will develop the external sourcing strategy for commercial and development portfolio for external contract testing laboratory. The CTL team is part of the External Supply organization is accountable for the execution of testing activities associated with the laboratory within scope.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Laboratory Supplier relationship management, including development and reporting of metrics and monitoring performance to continuously improve efficiency and effectiveness of suppliers.
Building and maintaining strong partnerships with all external laboratory functions to increase overall effectiveness and success of programs.
Ability to operate in highly matrixed teams.
Project management of a portfolio of cross-disciplinary external projects traversing the areas of Drug Product, Drug Substance, and Attribute Sciences.
Primary focus will be to manage delivery of analytical work packages (method qualification, method transfer, release testing, stability testing, characterization sample management ) with external contract laboratories
Actively participate in cross-functional teams with clear accountability for performance and ensure the quality, cost, and delivery of products from  Contract Testing Laboratory sites are consistently met, as well as lead issue resolution, problem solving and serve as an escalation agent.
Responsible to ensure analytical escalations are captured and communicated accurately and timely - Identification of project optimization opportunities (timeline, budget, technical execution), prioritization of a rolling portfolio of projects
Ensure that designated lead programs meet compliance, speed, quality, and cost targets through strong scientific and technical understanding of the programs and drug product development.
Identification of project optimization opportunities (timeline, budget, technical execution), prioritization of a rolling portfolio of projects
Supplier evaluation and selection
This position will require occasional domestic and international travel

 
What you need to apply:

Advanced degree in engineering or the sciences.
Experience in large molecule analytical development including method development, method qualifications/transfers/validations, release, stability and characterization testing.
Self-starter with a high-level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality results
Experience interfacing with domestic and international CTL /CRO organizations
Strong understanding of cGMP, Regulatory/CMC, legal, Quality requirements and import/export policies
Demonstrated understanding of drug development and commercialization for synthetic and/or biologic therapeutics
Experience as team member/leader of cross-functional and matrixed teams including effective writing, presentation, organizational and interpersonal skills to address a broad scope of audiences
Proven business acumen, high level strategic thinking, and strong analytical skills with the ability to structure, pragmatically scope, and solve complex problems
Demonstrated quantitative skills including experience in business process development, continuous improvement, operational excellence and performance management
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Management, Laboratory/Scientific, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Supply Chain Project Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-07 10:17:17]]></date><referencenumber><![CDATA[1715]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1715&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Supply Chain Project Manager to support our clients External Supply team based in Dublin. As Project Manager you will support projects in readiness for launch of high-volume supply of Medical Devices to the commercial market. 
 
 
 
Why you should apply:

This is an opportunity to lead high-impact, cross-functional supply chain projects that directly support the successful delivery of medical devices to patients
You will work at a strategic level, partnering closely with senior leadership and global stakeholders to shape and implement critical supply chain initiatives
The role offers exposure to end-to-end device supply operations, from supplier readiness and manufacturing through distribution and scale-up

 
What you will be doing:

Understand the scope of work for each project as defined by the Director for Device Supply
Develop project charters aligned with scope of project
Establish resources required for successful execution of project
Develop and manage project plans with clear objectives and milestone dates
Engage with internal and external stakeholders for successful execution of projects
Establish and maintain dashboards / scoreboards for each project to manage and communicate status
 Apply lean methodologies in execution of projects and apply a lesson learned approach in the interest of continuous improvements
Examples of projects to be managed include:
Defining and implementing an appropriate SKU strategy
Ensuring device specification requirements are met during manufacturing, storage, handling and transport
Implement an injection molding tooling maintenance and replacement strategy
Identify and implement improvements for volume scale up project
Ensure suppliers meet receiving sites requirements
Streamlined procurement, manufacture, supply and payment processes

 
What you need to apply:

Bachelor’s Degree in a Science, Engineering or Supply Chain discipline
Project management experience in pharmaceutical operations
Experience in medical devices with specific understanding of MDR’s
Knowledge and experience in application of continuous improvement, operational excellence methodologies such as lean six sigma

 
 ]]></description><jobtype><![CDATA[Remote, Contractor]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[Technical Services Specialist (Upstream and Downstream) ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-07 11:41:09]]></date><referencenumber><![CDATA[1716]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1716&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Technical Services Specialist (Upstream and Downstream) for our client based in Dublin.
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Excellent contracting rates on offer.

 
 
What you will be doing:

To provide process expertise in one, or both of the following disciplines:
 Upstream (Cell culture focus) to include media preparation, large scale cell culture bulk drug substance manufacturing process (vial thaw, scale up, seed reactors and production bioreactors and harvest centrifugation/clarification.
Downstream to include buffer preparation, purification and viral reduction steps including chromatography, ultrafiltration, viral reduction filtration and viral inactivation technologies and DS formulation, bulk fill and storage.
To author and review process transfer documentation, gap assessments, technical protocols and reports, clinical manufacturing documentation, process validation documentation, strategy documents etc...
To identify requirements for laboratory studies to support process fit, decisions or process transfer, and to liaise closely with Global Process Development to oversee the design and execution of studies.
To support the introduction of new raw materials and consumables through the generation of materials lists, Bills of Materials, material specifications and outline testing requirements
To work closely with colleagues in Quality, Supply Chain and Manufacturing Operations to ensure availability and release of materials to meet technology transfer and routine manufacturing timelines.
To identify and implement process improvements, e.g. yield, cycle time reduction
To generate documentation protocols and lead the execution of plant supporting studies and technical studies on the manufacturing floor at commercial scale.
May be required to work periodically out of normal business hours (temporary shift working) during periods of engineering and validation batch execution and provide on-call support to manufacturing.
To provide on the floor support for troubleshooting processing issues and to lead manufacturing investigations into process deviations and resolution.Lead any key process changes using change control system.
Adherence to highest standards for Compliance (Quality and Safety), implement corporate standards and liaise effectively with global groups and provide technical support during audits.
Ensure compliance with site EHS policy, cGMP and other business regulations and participate in risk assessments, audits, and incident investigations.
To author and review common technical document (CTD) sections and reports for regulatory agency submissions.
To serve as a subject-matter expert (SME) on technology transfer and process support during regulatory agency inspections.

 
 
What you need to apply:

Minimum 3+ years’ experience in Technical Services / Process Development / Manufacturing Support in a biological bulk drug substance manufacturing organization
Technical and operational knowledge of multiple unit operations in cell culture and or downstream purification processing
Comprehensive understanding of cGMP requirements for biopharmaceutical manufacturing
Good interpersonal skills coupled with demonstrated ability to effectively work in a matrix organization, and in local group settings
Ability to present and defend technical and scientific approaches in both written and verbal form
Ability to drive for results independently and adapt to rapidly changing priorities
Experience of Technology Transfer activities is advantageous
Experience of clinical manufacturing activities is advantageous
Knowledge or experience of start-up or systems would be ideal
Technical writing competency  
B.Sc. in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Engineering
M.Sc. or other postgraduate qualification in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Engineering.
Experience of authoring CMC sections of regulatory submissions

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Site Process and Cleaning Validation Lead]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-12 12:58:58]]></date><referencenumber><![CDATA[1718]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1718&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Site Process and Cleaning Validation Lead for a world-class, innovation-driven pharmaceutical manufacturing site. This role offers the opportunity to lead critical validation activities at a high-performing, globally regulated facility, working with advanced technologies and strong quality systems. The successful candidate will provide hands-on technical leadership across process and cleaning validation while influencing cross-functional teams, supporting audits, and driving continuous improvement in a patient-focused environment.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Develop and implement site-wide master plans for process and cleaning validation activities.
Lead the development, planning, and execution of validation strategies and PPQ protocols, including risk assessments, data evaluation, and technology transfer support.
Oversee the review, approval, and maintenance of validation documentation, reports, and change control records.
Partner cross-functionally with manufacturing, engineering, and quality teams to support continuous improvement initiatives.
Ensure full compliance with global regulatory standards (e.g., FDA, EMA) and internal quality policies.
Manage validation-related investigations, deviations, and the implementation of corrective and preventive actions (CAPAs).
Deliver training to site personnel on validation processes, expectations, and best practices.
Serve as the validation representative during internal audits, external audits, and regulatory inspections.
Participate in risk assessments and design reviews across all business units.
Track, analyze, and report weekly performance metrics (e.g., GTW, QMS, EHS, ComplianceWire).
Support audit readiness activities, actively engage during audits, and contribute to audit responses and follow-up actions, including participation in internal and external audit programs.
Manage revalidation schedules, regulatory response support, laboratory validation document reviews, and APR reporting in collaboration with business unit owners.
Coach, develop, and upskill direct reports to ensure strong technical capability and leadership support at the site level.
Lead, motivate, and communicate effectively with team members and management to drive engagement and performance.
Conduct performance evaluations in line with company policies, including individual development planning.
Maintain appropriate staffing levels aligned with business needs, including recruitment and selection.
Develop and manage departmental budgets to achieve organizational objectives.
Address underperforming KPIs by implementing robust and sustainable preventive action plans.

 
What you need to apply:

Minimum of 9+ years of experience with a Bachelor’s degree, 7+ years with a Master’s degree, or 5+ years with a PhD in a scientific or engineering discipline (e.g., Chemistry, Microbiology, Pharmacy, Chemical Engineering, or a related field). 
At least 7+ years of hands-on experience in pharmaceutical validation, including process and/or cleaning validation. 
Strong working knowledge of validation-related regulatory requirements and guidelines (cGMP, FDA, EMA, ICH Q7, Q8, Q9, Q10). 
Demonstrated strengths in project management, problem-solving, and organizational skills. 
Proven ability to work effectively in cross-functional teams while managing multiple priorities and projects. 
Excellent conflict resolution and stakeholder management skills. 
Subject matter expertise in key validation areas such as cleaning validation, CSV, aseptic processing, process validation, and CPV. 
Solid understanding of process validation, computer system validation, SCADA systems, continued process verification (CPV), sterilization, packaging systems, and associated technologies. 
Strong awareness of current data integrity expectations is highly desirable. 
Excellent written and verbal communication and presentation skills, with the ability to clearly and concisely present data to team members and senior management when required.
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[MES Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-22 09:34:41]]></date><referencenumber><![CDATA[1730]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1730&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[MES Engineer
 Team Horizon is seeking a MES Engineer for a client in Mayo. The purpose of this role is to maintain the MES environment; to author and maintain recipes &amp;amp; worksheets. As well as troubleshooting ad providing solutions for MES and SAP problems in recipe execution and recipe authoring.
 Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 What you will be doing:

Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material spec's including phase transition logic
Design, create, write and execute, test and validation protocols, risk assessments, and system documentation.
Design, create, write and/or make all required changes to ensure cleaning, equipment and product procedures are aligned to MES processes and vice versa.
Design, create, write and provide training for all other site personnel on their related MES roles and arrange system access.
Participate in MES knowledge exchanges, MES Governance meetings and manage issues, work-arounds and fixes identified.
Liaise with the Global MES on the sites required system improvements.
Provide support to other MES system users as required to ensure business continuity.
Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.
Keep other recipe authors up to date on MES changes
Documentation of all activities in line with cGMP requirements.
Cross training within the team and training of new team members.
Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
Adheres to and supports all EHS standards, procedures and policies. 

What you need to apply:

Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.
A minimum of  2 years authoring experience preferably using POMSnet.
Be familiar with MES application and configuration rules and requirements including interfacing (preferably POMSnet).
Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.
A good knowledge of IT systems is required for this role.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Digital Transformation Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-22 09:52:32]]></date><referencenumber><![CDATA[1731]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1731&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Digital Transformation Project Manager
Team Horizon is seeking a Digital Transformation Project Manager for a client in Mayo. This role oversees a portfolio of digital transformation initiatives designed to enhance operational efficiency, optimize manufacturing processes, and drive a culture of innovation and excellence.
The ideal candidate brings a strong understanding of digital technologies, project management methodologies, and the biopharmaceutical industry, with the ability to translate strategy into impactful execution.
 Why you should apply:

Contribute your passion and expertise in digital transformation to impact the future of manufacturing and set new standards for operational excellence. You will play a key role in my clients digital transformation journey.
You’ll work in a dynamic, collaborative environment where your ideas are valued, your voice matters, and your expertise directly shapes the future of the organisation.
Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.

What you will be doing:

Coordinate a portfolio of digital transformation projects, liaising with above-site teams and SMEs to represent the Westport site.
Collaborate with leadership to develop and implement digital strategies supporting operational and business goals.
Collaborate with cross-functional teams, including IT, operations, regulatory affairs, and quality assurance, to gather requirements and ensure alignment of project goals.
Drive value analysis and business case development for both new and existing digitalization projects
Communicate project status, risks, and milestones to stakeholders at various levels.
Develop and implement change management strategies to ensure broad user acceptance and successful adoption of initiatives.
Represent the Business/Site in the deployment of digital tools and technologies, including system architecture and configuration discussions, acting as the operations/business voice in technical forums.
Lead cross-functional teams in project delivery, ensuring projects are completed on time, within scope, and with clear stakeholder engagement.
Establish and monitor KPIs to measure the success and performance of digital transformation initiatives.
Ensure all initiatives comply with relevant regulations and standards.

 What you need to apply:

Bachelor’s degree in Business Administration, Information Technology, Engineering, or a related field.
Proven experience in digital transformation and project management, preferably in a manufacturing or biopharmaceutical environment.
Experience in Lean, Six Sigma, or other process improvement methodologies.
Knowledge of or strong interest in digitalization, technology, and operational excellence principles (e.g., IoT, AI, robotics).
Excellent project and portfolio management skills, with the ability to multitask and manage cross-functional resources.
Strong communication, analytical, and problem-solving skills; demonstrated ability to influence stakeholders at all levels.

Preferred qualifications

Master’s degree in a related area is advantageous.
Certifications such as Lean Six Sigma Black Belt, PMP, or credentials related to Industry 4.0.
Experience with Industry 4.0 technologies and leading digital manufacturing projects.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Automation Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-12 10:18:26]]></date><referencenumber><![CDATA[1739]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1739&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Automation Engineer
Team Horizon is seeking an Automation Engineer for a pharmaceutical client in Dublin who will support day to day operation of complex automation systems.
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Safety: Support a safe working environment by complying with all pertinent environmental health/safety practice and regulations.
Maintain: Be the System Owner for automation systems in a GMP-regulated manufacturing setting ensuring systems are maintained in the validated state.
Investigate: Lead and support incident investigations and troubleshooting efforts related to manufacturing automation systems.
Improve: Implement improvements related to corrective or preventative actions; including software changes, and updates to design documentation and standard operating procedures.
Innovate: Analyse the design of current systems, to recommend continuous improvements in line with the latest technology and regulatory standards. Support new product or technology introductions by performing engineering assessments, implementing automation system changes, and supporting engineering runs.

What you need to apply:

Bachelor’s degree in Automation Engineering, Electrical Engineering, Computer Science, Chemical Engineering, Biotech Engineering, or related life science engineering with 5+ years’ experience in operations/manufacturing environment.
Background in automation design, installation, programming. Experience with validation and lifecycle maintenance is an advantage.
Experience in one of the following automation specialties is an advantage:

Building Management Systems (Siemens Desigo)
Clean Utilities generation and distribution (Rockwell or Siemens PLCs)
Biopharmaceutical Formulation and/or Fill/Finish (Rockwell or Siemens PLCs)
Inspection or Packaging facilities (Rockwell / B&amp;amp;R / Siemens PLCs)
Experience in programming and troubleshooting of PLC, HMI, SCADA, Serialisation and Vision Systems. The systems include:

PLCs: Siemens S7-300/400/1500, B&amp;amp;R, and Rockwell
HMIs: Siemens and Rockwell.
SCADA: iFix, InTouch, Zenon, PCS7, and Rockwell FTView. FT Batch.
Fieldbus: ControlNet, DeviceNet, Profibus, Profinet, AS-I, BACnet etc.
 Vision Systems: Cognex, Keyence


Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards, 21 CFR Part 11 and Annex 11.
Working knowledge of network architecture technologies including TCP/IP and Firewalls.
Independent, self-motivated, organised, and able to multi-task in a manufacturing environment
Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
Solid technical writing, and communication/presentation skills.
Proficient in managing relationships with stakeholders; coordinating and collaborating with teams from different departments to achieve common goals.
Travel at various times may be required to support training and vendor visits.


]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Sr Associate QC (Senior) -Equipment Support Role]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-24 09:31:21]]></date><referencenumber><![CDATA[1744]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1744&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a IE CW Sr Associate QC (Senior) -Equipment Support Role with our client based in Dublin. Responsible for planning, executing and documenting the qualification, calibration and routine maintenance of laboratory systems for cGMP Quality Control laboratory facilities. Responsible for ensuring that all maintenance &amp;amp; calibration activities carried out by Calibration Technicians are tracked &amp;amp; managed through the Computerised Maintenance Management System (CMMS) Maximo. Responsible for authoring/owning and approving Validation Life Cycle documents for computer related systems including responsibility for Data Integrity testing and business administration of Laboratory Computer Related systems. Responsible for the execution of protocols once approved.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

 Planning and conducting routine calibration, requalification and maintenance of laboratory equipment ensuring calibration and maintenance schedules are adhered to as per CMMS Maximo
Reviewing &amp;amp; filing of QC calibration &amp;amp; maintenance documentation.
Planning, executing and documenting the qualification of new laboratory equipment in a cGMP regulated environment, including the writing of equipment validation protocols and associated summary reports.
Conduct periodic reviews of instrument validation as part of validation life cycle.
Alerting Quality Control Management in the event of equipment failing to meet calibration or qualification requirements and conducting impact assessments/investigations as required.
Scheduling and coordination of equipment repairs and maintenance with vendors/contractors, while minimizing level of down-time for lab equipment, and disruption to laboratory activities.
Participation in technical project teams to act as a subject matter expert on instrument validation regulations and procedures.
Where applicable, owns and project manages change controls and adherence to Change Control metrics
Supporting and managing the addition of project components to CMMA Maximo
Act as a key contributor and sponsor to Data Integrity Assessments for Lab systems
Any other tasks/projects assigned as per manger’s request

 
What you need to apply:

Bachelor’s degree in a Science related field is required.
Minimum of 3 years of laboratory experience in a cGMP laboratory environment including exposure to analytical instrument validation and data integrity assessments.
Detailed knowledge of the methodology, and instrumentation and analytical techniques used for biopharmaceutical testing.
Understanding of current regulatory requirements for cGMP laboratory equipment validation and electronic record integrity.
Demonstrated success in managing an equipment qualification or maintenance program advantageous.
]]></description><jobtype><![CDATA[Remote, Contractor]]></jobtype><category><![CDATA[Engineering, Laboratory/Scientific]]></category></job><job><title><![CDATA[QC Biochemistry]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-24 09:40:24]]></date><referencenumber><![CDATA[1745]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1745&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QC Biochemistry for our client based in Dublin. The individual in this position should have a working knowledge of the cGMP QC laboratory environment and laboratory equipment associated with biopharmaceutical analysis. The QC Biochemistry Senior Analyst is responsible for providing technical and laboratory support to the QC analysts in Dublin specifically working with the team to troubleshoot issues that may arise. The position requires the ability to understand and follow written SOPs, to accurately and legibly record work in real time, and pay close attention to detail. The individual must be able to perform routine tasks with a minimum of supervision.
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Excellent contracting rates on offer.

 
What you will be doing:

Perform all lab functions in compliance with cGMP
Follow written procedures for the following tests, as trained and qualified: Gel electrophoresis (SDS-PAGE, IEF), ELISA and plate based assays (potency and residual assays such as HCP and ProA)
Stability scheduling and testing.
Recognize and report aberrant test results and sample conditions.
Provide QC SME and day to day technical guidance to QC biochemistry analysts.
Training of new analysts in specific assays.
Drive continuous improvement initiatives within the QC department.
Lead and complete execution of investigations/CAPAs in a timely manner.
Provide lab support including reagent preparation, cleaning, and routine equipment maintenance.
Ensure training is current for all job functions performed.
Order, stock and receive laboratory supplies.
Complete all required documentation legibly and accurately.

 
What you need to apply:

BSc in Chemistry or a biological science, with 4-7 years’ experience, or equivalent combination of education and experience.
A working knowledge of the cGMP QC laboratory environment, and equipment associated with testing of biopharmaceutical products
Ability to follow written procedures with close attention to detail
Ability to function with minimal supervision for routine job duties.

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Operations Aseptic Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-24 09:46:17]]></date><referencenumber><![CDATA[1746]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1746&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Engineering Aseptic Specialist for our client based in Sligo. As an Aseptic Operations Specialist, you will act as a site subject matter expert for aseptic manufacturing and sterility assurance. You will provide technical and operational support across aseptic processes, partner closely with cross-functional teams, and help ensure that manufacturing activities are carried out in line with regulatory requirements, site procedures, and standards.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Act as a site subject matter expert for aseptic manufacturing.
Provide key input into manufacturing process setup and batch record design.

Ensure operations procedures for aseptic manufacturing are compliant with relevant safety, environmental, GMP, and regulatory requirements, as well as network aseptic best practice.

Apply risk management tools to drive aseptic performance and sterility assurance, including pFMEA and What If/HAZOP assessments.
Partner with Quality, Engineering, Aseptic MQA, Aseptic Mentors, and other site SMEs to support manufacturing shifts and ensure safe, timely, and quality completion of product batches.
Observe aseptic technique and behaviors on the floor and provide coaching and feedback where appropriate, particularly during critical activities such as cleaning, sanitization, aseptic setup, EM plate handling, and interventions.
Lead and support investigations into sterility, media fill, environmental monitoring excursions, and EMPQ issues, and help establish root cause and CAPA.
Own the analysis and trending of environmental monitoring data, including facility and personnel monitoring, and develop action plans in response to trends.
Contribute to the ongoing development and implementation of best practices in aseptic manufacturing.
Support the site contamination control strategy, aseptic processing strategy, and long-range planning related to aseptic manufacturing.
Provide input into cleanroom, equipment, and utility design, qualification and re-qualification, preventive maintenance strategies, and real-time monitoring.
Support regulatory audits and inspections as an aseptic and sterility assurance subject matter expert.
Support training of operations personnel in aseptic technique and aseptic processing procedures
Participate in routine leadership GEMBAs in manufacturing and testing areas.
Perform other duties as assigned.

 
What you need to apply:

Level 8 NFQ degree in Science, Quality, or Engineering.
Minimum 5 years’ experience in a GMP environment.
Minimum 3 years’ experience supporting aseptic manufacturing.
Strong knowledge of regulatory requirements.
Strong communication skills, both written and verbal
Project management experience. Experience supporting regulatory inspections, including HPRA and FDA.
Experience in microbiology.
Experience working in a sterile, aseptic, or pharmaceutical environment.  
Strong knowledge of aseptic and sterile processes.
Working knowledge of current EU, FDA, ICH, HPRA, and Annex 1 requirements.
High attention to detail and strong concentration.
Proven problem-solving skills and ability to adapt to changing requirements. Innovative mindset with the ability to propose and implement new solutions.
Results-driven with a commitment to meeting targets and metrics. Strong prioritization and time management skills.
Excellent interpersonal and collaboration skills.
A strong commitment to quality, integrity, and right-first-time performance.
Ability to work independently in a largely self-managed environment while engaging effectively with the wider team.
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Site Validation Lead ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-24 11:50:47]]></date><referencenumber><![CDATA[1747]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1747&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Site Process and Cleaning Validation Lead for a world-class, innovation-driven pharmaceutical manufacturing site. This role offers the opportunity to lead critical validation activities at a high-performing, globally regulated facility, working with advanced technologies and strong quality systems. The successful candidate will provide hands-on technical leadership across process and cleaning validation while influencing cross-functional teams, supporting audits, and driving continuous improvement in a patient-focused environment.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Develop and implement site-wide master plans for process and cleaning validation activities.
Lead the development, planning, and execution of validation strategies and PPQ protocols, including risk assessments, data evaluation, and technology transfer support.
Oversee the review, approval, and maintenance of validation documentation, reports, and change control records.
Partner cross-functionally with manufacturing, engineering, and quality teams to support continuous improvement initiatives.
Ensure full compliance with global regulatory standards (e.g., FDA, EMA) and internal quality policies.
Manage validation-related investigations, deviations, and the implementation of corrective and preventive actions (CAPAs).
Deliver training to site personnel on validation processes, expectations, and best practices.
Serve as the validation representative during internal audits, external audits, and regulatory inspections.
Participate in risk assessments and design reviews across all business units.
Track, analyze, and report weekly performance metrics (e.g., GTW, QMS, EHS, ComplianceWire).
Support audit readiness activities, actively engage during audits, and contribute to audit responses and follow-up actions, including participation in internal and external audit programs.
Manage revalidation schedules, regulatory response support, laboratory validation document reviews, and APR reporting in collaboration with business unit owners.
Coach, develop, and upskill direct reports to ensure strong technical capability and leadership support at the site level.
Lead, motivate, and communicate effectively with team members and management to drive engagement and performance.
Conduct performance evaluations in line with company policies, including individual development planning.
Maintain appropriate staffing levels aligned with business needs, including recruitment and selection.
Develop and manage departmental budgets to achieve organizational objectives.
Address underperforming KPIs by implementing robust and sustainable preventive action plans.

 
What you need to apply:

Minimum of 9+ years of experience with a Bachelor’s degree, 7+ years with a Master’s degree, or 5+ years with a PhD in a scientific or engineering discipline (e.g., Chemistry, Microbiology, Pharmacy, Chemical Engineering, or a related field). 
At least 7+ years of hands-on experience in pharmaceutical validation, including process and/or cleaning validation. 
Strong working knowledge of validation-related regulatory requirements and guidelines (cGMP, FDA, EMA, ICH Q7, Q8, Q9, Q10). 
Demonstrated strengths in project management, problem-solving, and organizational skills. 
Proven ability to work effectively in cross-functional teams while managing multiple priorities and projects. 
Excellent conflict resolution and stakeholder management skills. 
Subject matter expertise in key validation areas such as cleaning validation, CSV, aseptic processing, process validation, and CPV. 
Solid understanding of process validation, computer system validation, SCADA systems, continued process verification (CPV), sterilization, packaging systems, and associated technologies. 
Strong awareness of current data integrity expectations is highly desirable. 
Excellent written and verbal communication and presentation skills, with the ability to clearly and concisely present data to team members and senior management when required.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Talent Acquisition Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-24 11:52:40]]></date><referencenumber><![CDATA[1748]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1748&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Are you a proactive recruiter who loves finding top talent in fast-paced environments? We’re looking for a Talent Acquisition Specialist to join our clients team and help shape the future of hiring in our organisation.
 
 
Why you should apply:

You’ll work in a dynamic, collaborative environment where your ideas are valued, your voice matters, and your expertise directly shapes the future of the organisation.
If you’re driven, curious, and ready for the next step, this role is where you can thrive

 
What you will be doing:

Recruitment will be focused on a specific team/function, or other areas as assigned.
Responsible for attracting top talent and developing a strong, qualified candidate pool for current and future openings.
Additional job duties include pre-screening candidates, project management, partnering with team members to develop sourcing strategies and providing talent for open positions.
Demonstrate ability to proactively identify, source and manage talent pools aligned to business priorities.
Core responsibility is to manage open job requisitions, update and manage SmartRecruiters, achieve recruiting metrics and report key accomplishments.
Will also compile and communicate the knowledge base, industry overviews, and market trends, data and analytics to team members and business leaders.
Will prepare and approve offer packages, providing equity &amp;amp; market competitiveness data research.
Ensure compliance to state/federal employment laws and policies and practices for applicant tracking compliance and reporting metrics.
Establish a true business partnership with hiring managers and leadership on all staffing related activities and issues.

 
What you need to apply:

Bachelor's degree required.
2-3+ years recruitment experience in a competitive, fast-paced environment required.
Must project a strong business presence and have the ability to instill confidence in clients and to deliver results.
Proactive recruiting and sourcing experience required.
Healthcare/Pharmaceutical industry recruitment experience strongly preferred.
Experience in managing requisitions within SmartRecruiters preferred.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[Talent Acquisition Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-24 11:52:40]]></date><referencenumber><![CDATA[1748-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1748&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Are you a proactive recruiter who loves finding top talent in fast-paced environments? We’re looking for a Talent Acquisition Specialist to join our clients team and help shape the future of hiring in our organisation.
 
 
Why you should apply:

You’ll work in a dynamic, collaborative environment where your ideas are valued, your voice matters, and your expertise directly shapes the future of the organisation.
If you’re driven, curious, and ready for the next step, this role is where you can thrive

 
What you will be doing:

Recruitment will be focused on a specific team/function, or other areas as assigned.
Responsible for attracting top talent and developing a strong, qualified candidate pool for current and future openings.
Additional job duties include pre-screening candidates, project management, partnering with team members to develop sourcing strategies and providing talent for open positions.
Demonstrate ability to proactively identify, source and manage talent pools aligned to business priorities.
Core responsibility is to manage open job requisitions, update and manage SmartRecruiters, achieve recruiting metrics and report key accomplishments.
Will also compile and communicate the knowledge base, industry overviews, and market trends, data and analytics to team members and business leaders.
Will prepare and approve offer packages, providing equity &amp;amp; market competitiveness data research.
Ensure compliance to state/federal employment laws and policies and practices for applicant tracking compliance and reporting metrics.
Establish a true business partnership with hiring managers and leadership on all staffing related activities and issues.

 
What you need to apply:

Bachelor's degree required.
2-3+ years recruitment experience in a competitive, fast-paced environment required.
Must project a strong business presence and have the ability to instill confidence in clients and to deliver results.
Proactive recruiting and sourcing experience required.
Healthcare/Pharmaceutical industry recruitment experience strongly preferred.
Experience in managing requisitions within SmartRecruiters preferred.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[Talent Acquisition Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-24 11:52:40]]></date><referencenumber><![CDATA[1748-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1748&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Are you a proactive recruiter who loves finding top talent in fast-paced environments? We’re looking for a Talent Acquisition Specialist to join our clients team and help shape the future of hiring in our organisation.
 
 
Why you should apply:

You’ll work in a dynamic, collaborative environment where your ideas are valued, your voice matters, and your expertise directly shapes the future of the organisation.
If you’re driven, curious, and ready for the next step, this role is where you can thrive

 
What you will be doing:

Recruitment will be focused on a specific team/function, or other areas as assigned.
Responsible for attracting top talent and developing a strong, qualified candidate pool for current and future openings.
Additional job duties include pre-screening candidates, project management, partnering with team members to develop sourcing strategies and providing talent for open positions.
Demonstrate ability to proactively identify, source and manage talent pools aligned to business priorities.
Core responsibility is to manage open job requisitions, update and manage SmartRecruiters, achieve recruiting metrics and report key accomplishments.
Will also compile and communicate the knowledge base, industry overviews, and market trends, data and analytics to team members and business leaders.
Will prepare and approve offer packages, providing equity &amp;amp; market competitiveness data research.
Ensure compliance to state/federal employment laws and policies and practices for applicant tracking compliance and reporting metrics.
Establish a true business partnership with hiring managers and leadership on all staffing related activities and issues.

 
What you need to apply:

Bachelor's degree required.
2-3+ years recruitment experience in a competitive, fast-paced environment required.
Must project a strong business presence and have the ability to instill confidence in clients and to deliver results.
Proactive recruiting and sourcing experience required.
Healthcare/Pharmaceutical industry recruitment experience strongly preferred.
Experience in managing requisitions within SmartRecruiters preferred.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[API Engineering Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-25 11:44:05]]></date><referencenumber><![CDATA[1749]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1749&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a API Engineering Manager for a leading pharmaceutical company in Sligo.
This position reports to the Operations Engineering Manager and is responsible for leading and managing a team comprising of engineers, technicians, and apprentices. The Engineering Manager support our API (Active Pharmaceutical Ingredients) business unit. 
Your role will involve team development, budget management, liaising with production and ensuring compliance with policies related to Personnel, Quality, Engineering, Safety and Finance.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

This is a varied position which requires cross-functional collaboration with contract maintenance providers, production, technical operations, quality and other personnel to ensure equipment performance is maximized. Your role will involve working on a variety of projects ranging from continuous improvement to new product introductions.
Establish in conjunction with the Operations Engineering Manager the department goals, schedules and timetables for activities. 
Assist with the management and support of manufacturing equipment development. 
Support the API Engineering Team in ensuring that manufacturing equipment is maintained to meet the required legal, divisional and corporate standards. 
Prepare appropriate CAPA plans and implement timelines. 
Undertake specific investigations, and equipment monitoring, with a view to improve manufacturing performance e.g., reducing plant downtime and maximizing Plant output and yield.   
Implementation of equipment/process upgrade in an environment of continuous improvement. 
Develop monthly engineering metrics and provide management reports in a timely manner. 
Ensure relevant budgets are within target and prepare capital expenditure requests for plant as required.
Ensure successful external, Division and Corporate audits. 
Ensure safety standards are met, and safe working practices are adhered to.  
Manage internal and external plant projects as needed. 
Supervise and manage relationships with external contractors. 
Attend relevant meetings and drive actions to closure. 
Any other duties as assigned.

 
What you need to apply:

Degree (Level 7 or above) in engineering or scientific area (Chemistry)
Minimum of 6 years pharmaceutical industry with a minimum of 2 years’ experience as an Engineering Supervisor.
Previous experience in an active pharmaceutical manufacturing facility, particularly within the Engineering Department, is required.
Experience with glass lined vessels, reactors, pumps, heat exchangers, ATEX, solvent handling. High level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures.
Strong problem-solving skills with the ability to make prompt decisions on engineering related issues
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Quality Engineer - Design Assurance ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-09 14:00:20]]></date><referencenumber><![CDATA[1756]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1756&amp;Itemid=986]]></url><city><![CDATA[Clare]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Quality Engineer Design Assurance for a global Med Tech company. Acting as the Quality representative on project core teams, you will oversee design controls, risk management, and change control processes while driving adherence to global regulatory requirements. Your responsibilities will span from product inception through launch and maintenance, requiring strong collaboration with cross-functional teams and effective communication skills.
 
 
Why you should apply:

You will play a key role in ensuring that new product development and sustaining projects meet stringent quality and compliance standards.
Join a company where imagination and passion,  design and engineering find transformative solutions that turn dreams into possibilities.

 
What you will be doing:

Be the Design Assurance Quality Engineer on project core teams for design change projects and develop close relationships with core team members and extended quality functions as needed for the project.
Contribute to the formation and ongoing management of DHF documentation
Lead risk management activities within the project.
Drive compliance management activities (e.g., IEC 60601) on the project with support from the Compliance Engineer.
Demonstrate a patient-first approach to quality engineering.
Support the creation and implementation of verification and validation activities.
Work closely with R&amp;amp;D functions to ensure comprehensive testing of product requirements and the execution of the V&amp;amp;V plan.
Review and approve testing procedures and documentation.
Review and challenge the statistical rationale and data analysis within the test protocol and reports.
Assess and authorise related execution deviations.
Assist/conduct Failure investigations and problem-solving sessions.
Responsible for the software issue tracking process per IEC 62304 to ensure software issues are logged, risk assessed and dispositioned appropriately.
Ensure compliance across projects for design control, risk management, and change control processes.
Advocate for a strong quality culture within project core teams
Support of other QMS activities outside of projects, such as CAPA, Field Assessment and operations engineering assessments.

 
What you need to apply:

A relevant degree or equivalent experience (engineering degree preferred), or a minimum of 5 years of quality engineering experience as an equivalent qualification 
Knowledge in working with ISO 13485, QSR, ISO 14971, and statistical techniques
Expertise in design assurance, including design controls, standards compliance, and risk management
Strong written and verbal communication skills 
Strong organisational skills 
Experience with MDR – advantage 
Experience with IEC 62304 and IEC 62366 – advantage 
Ability to influence. 

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Senior Quality Engineer - Design Assurance ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-09 14:00:20]]></date><referencenumber><![CDATA[1756-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1756&amp;Itemid=986]]></url><city><![CDATA[Limerick]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Quality Engineer Design Assurance for a global Med Tech company. Acting as the Quality representative on project core teams, you will oversee design controls, risk management, and change control processes while driving adherence to global regulatory requirements. Your responsibilities will span from product inception through launch and maintenance, requiring strong collaboration with cross-functional teams and effective communication skills.
 
 
Why you should apply:

You will play a key role in ensuring that new product development and sustaining projects meet stringent quality and compliance standards.
Join a company where imagination and passion,  design and engineering find transformative solutions that turn dreams into possibilities.

 
What you will be doing:

Be the Design Assurance Quality Engineer on project core teams for design change projects and develop close relationships with core team members and extended quality functions as needed for the project.
Contribute to the formation and ongoing management of DHF documentation
Lead risk management activities within the project.
Drive compliance management activities (e.g., IEC 60601) on the project with support from the Compliance Engineer.
Demonstrate a patient-first approach to quality engineering.
Support the creation and implementation of verification and validation activities.
Work closely with R&amp;amp;D functions to ensure comprehensive testing of product requirements and the execution of the V&amp;amp;V plan.
Review and approve testing procedures and documentation.
Review and challenge the statistical rationale and data analysis within the test protocol and reports.
Assess and authorise related execution deviations.
Assist/conduct Failure investigations and problem-solving sessions.
Responsible for the software issue tracking process per IEC 62304 to ensure software issues are logged, risk assessed and dispositioned appropriately.
Ensure compliance across projects for design control, risk management, and change control processes.
Advocate for a strong quality culture within project core teams
Support of other QMS activities outside of projects, such as CAPA, Field Assessment and operations engineering assessments.

 
What you need to apply:

A relevant degree or equivalent experience (engineering degree preferred), or a minimum of 5 years of quality engineering experience as an equivalent qualification 
Knowledge in working with ISO 13485, QSR, ISO 14971, and statistical techniques
Expertise in design assurance, including design controls, standards compliance, and risk management
Strong written and verbal communication skills 
Strong organisational skills 
Experience with MDR – advantage 
Experience with IEC 62304 and IEC 62366 – advantage 
Ability to influence. 

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Cleaning Validation Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-12 11:23:29]]></date><referencenumber><![CDATA[1757]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1757&amp;Itemid=986]]></url><city><![CDATA[Meath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Cleaning Validation Manager on an initial. As SME you will provide cleaning validation expertise and leadership to a team of specialists supporting technology transfer, cleaning validation, and routine monitoring of commercial manufacturing for Upstream and Downstream manufacturing.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Excellent contracting rates on offer.

 
 
What you will be doing:

Minimum of 10 years’ experience in a pharmaceutical manufacturing organization, with expertise in Bulk Drug Substance manufacturing, with previous experience in Cleaning Validation of cell culture unit operations and/or downstream unit operations.
Previous experience of cleaning cycle development or cleaning cycle improvement in a technical role is advantageous.
Proven expertise in leadership including demonstrated ability to drive for results and lead innovation and change.
Comprehensive understanding of cGMP requirements for commercial biopharmaceutical manufacturing and the ability to implement best practices to ensure multi-product bulk drug manufacturing operations are cGMP compliant.
Good interpersonal skills coupled with demonstrated ability to effectively work in a cross-functional global environment matrix organization, and in local group settings.
Ability to develop, build, present and defend technical and scientific approaches in both written and verbal form.
Can effectively partner with and influence stakeholders without direct solid line authority. Drives technical decisions balancing product quality and operational requirements.
Ability to drive for results independently and adapt to rapidly changing priorities.
Experience of leading Cleaning Validation teams is advantageous.
Excellent communication skills, and able to effectively influence across all levels of the organization both internal and external.
Detail orientated.
Technical writing competency.
Self-driven, able to prioritize, and to orchestrate multiple activities at once.
Consistently demonstrate sound business judgment when making decisions.
Ability to deal with ambiguity and complexity and influence others across levels of the organization

What you need to apply:

Minimum undergraduate degree in chemistry, biology, engineering or related discipline.
An advanced degree (MS, PhD) in Scientific (Biochemistry, Biology, Chemistry, Pharmacy) or Engineering (Chemical, Mechanical) related field is desirable.
Experience of authoring CMC sections of regulatory submissions 
Previous leadership experience of Cleaning Validation activites

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Cleaning Validation Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-12 11:23:29]]></date><referencenumber><![CDATA[1757-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1757&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Cleaning Validation Manager on an initial. As SME you will provide cleaning validation expertise and leadership to a team of specialists supporting technology transfer, cleaning validation, and routine monitoring of commercial manufacturing for Upstream and Downstream manufacturing.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Excellent contracting rates on offer.

 
 
What you will be doing:

Minimum of 10 years’ experience in a pharmaceutical manufacturing organization, with expertise in Bulk Drug Substance manufacturing, with previous experience in Cleaning Validation of cell culture unit operations and/or downstream unit operations.
Previous experience of cleaning cycle development or cleaning cycle improvement in a technical role is advantageous.
Proven expertise in leadership including demonstrated ability to drive for results and lead innovation and change.
Comprehensive understanding of cGMP requirements for commercial biopharmaceutical manufacturing and the ability to implement best practices to ensure multi-product bulk drug manufacturing operations are cGMP compliant.
Good interpersonal skills coupled with demonstrated ability to effectively work in a cross-functional global environment matrix organization, and in local group settings.
Ability to develop, build, present and defend technical and scientific approaches in both written and verbal form.
Can effectively partner with and influence stakeholders without direct solid line authority. Drives technical decisions balancing product quality and operational requirements.
Ability to drive for results independently and adapt to rapidly changing priorities.
Experience of leading Cleaning Validation teams is advantageous.
Excellent communication skills, and able to effectively influence across all levels of the organization both internal and external.
Detail orientated.
Technical writing competency.
Self-driven, able to prioritize, and to orchestrate multiple activities at once.
Consistently demonstrate sound business judgment when making decisions.
Ability to deal with ambiguity and complexity and influence others across levels of the organization

What you need to apply:

Minimum undergraduate degree in chemistry, biology, engineering or related discipline.
An advanced degree (MS, PhD) in Scientific (Biochemistry, Biology, Chemistry, Pharmacy) or Engineering (Chemical, Mechanical) related field is desirable.
Experience of authoring CMC sections of regulatory submissions 
Previous leadership experience of Cleaning Validation activites

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Quality Manager &amp; QP ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-12 18:50:26]]></date><referencenumber><![CDATA[1758]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1758&amp;Itemid=986]]></url><city><![CDATA[Wicklow]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QP &amp;amp; Quality Manager to play a crucial role in maintaining top quality and compliance in manufacturing processes for our client’s facility in Dublin. This opportunity lets you work in a dynamic environment - passionate about innovation and excellence. You will lead efforts to ensure our products meet strict European Legislation and company standards.
 
 
Why you should apply:

A job where you will find purpose and pride, where your work makes a difference.
Join a team driven by a culture of courage, trust, and collaboration where you strive for efficient and effective operations
Competetive Salary &amp;amp; benefits package

 
What you will be doing:

Ensure the  site follows Good Manufacturing Practice for Medicinal Products for Human Use. This is according to Eudralex Volume 4 of &quot;The rules governing medicinal products in the European Union.&quot; Follow Commission Directive 2003/94/EEC, its amendments, and any company requirements.
Act as a Qualified Person (QP) responsible for implementing the quality management system. Lead all aspects of the products release process. Ensure strict adherence to regulatory and customer requirements.
Serve as the primary contact with the regulatory agency (HPRA) regarding Manufacturing Licence, GMP inspections, and any potential product quality issues.
Develop and maintain an internal review process to ensure continuous compliance, preparing the site for audits at any time.
Lead and manage the audit process for the facility, ensuring that audit findings are thoroughly investigated and addressed promptly.
Measure and analyze site quality metrics and indicators, comparing performance against targets, and implement data-driven actions for continuous improvement of processes and products.
Develop and implement risk management strategies to minimize product and process risks, ensuring patient safety.
Coordinate the management, execution, and approval of quality documents and records for the site, including Nonconformance investigations, CAPA plans, Change Controls, SOPs, Validation Protocols, and Report

 
What you need to apply:

6-10 years’ experience of Quality implementation in Pharma industry
Proven knowledge or experience in applicable regulations and standards e.g. EU GMP Annex 1 particularly in relation to aseptic manufacturing environments.
Proven aseptic manufacture experience with knowledge in Sterility assurance and risk management.
Proven leadership experience with a track record of consistently meeting results.
Ability to operate effectively in a fast-paced environment and prioritize multiple tasks.
Proven ability to manage/supervise a large and diverse team of employees.
Strong leadership skills to motivate teams, make decisions and guide the organization toward quality objective.
Excellent organizational skills for managing tasks, coordinating resources, and ensuring prompt quality data driven decision making.
Excellent communication and interpersonal skills to build relationships with collaborators and facilitate collaboration with other functions.
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Quality Manager &amp; QP ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-12 18:50:26]]></date><referencenumber><![CDATA[1758-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1758&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QP &amp;amp; Quality Manager to play a crucial role in maintaining top quality and compliance in manufacturing processes for our client’s facility in Dublin. This opportunity lets you work in a dynamic environment - passionate about innovation and excellence. You will lead efforts to ensure our products meet strict European Legislation and company standards.
 
 
Why you should apply:

A job where you will find purpose and pride, where your work makes a difference.
Join a team driven by a culture of courage, trust, and collaboration where you strive for efficient and effective operations
Competetive Salary &amp;amp; benefits package

 
What you will be doing:

Ensure the  site follows Good Manufacturing Practice for Medicinal Products for Human Use. This is according to Eudralex Volume 4 of &quot;The rules governing medicinal products in the European Union.&quot; Follow Commission Directive 2003/94/EEC, its amendments, and any company requirements.
Act as a Qualified Person (QP) responsible for implementing the quality management system. Lead all aspects of the products release process. Ensure strict adherence to regulatory and customer requirements.
Serve as the primary contact with the regulatory agency (HPRA) regarding Manufacturing Licence, GMP inspections, and any potential product quality issues.
Develop and maintain an internal review process to ensure continuous compliance, preparing the site for audits at any time.
Lead and manage the audit process for the facility, ensuring that audit findings are thoroughly investigated and addressed promptly.
Measure and analyze site quality metrics and indicators, comparing performance against targets, and implement data-driven actions for continuous improvement of processes and products.
Develop and implement risk management strategies to minimize product and process risks, ensuring patient safety.
Coordinate the management, execution, and approval of quality documents and records for the site, including Nonconformance investigations, CAPA plans, Change Controls, SOPs, Validation Protocols, and Report

 
What you need to apply:

6-10 years’ experience of Quality implementation in Pharma industry
Proven knowledge or experience in applicable regulations and standards e.g. EU GMP Annex 1 particularly in relation to aseptic manufacturing environments.
Proven aseptic manufacture experience with knowledge in Sterility assurance and risk management.
Proven leadership experience with a track record of consistently meeting results.
Ability to operate effectively in a fast-paced environment and prioritize multiple tasks.
Proven ability to manage/supervise a large and diverse team of employees.
Strong leadership skills to motivate teams, make decisions and guide the organization toward quality objective.
Excellent organizational skills for managing tasks, coordinating resources, and ensuring prompt quality data driven decision making.
Excellent communication and interpersonal skills to build relationships with collaborators and facilitate collaboration with other functions.
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Documentation Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-19 10:03:12]]></date><referencenumber><![CDATA[1762]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1762&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Documentation Specialist for our client based in Sligo.
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site.

 
What you will be doing:

Co-ordinate and/or execute internal and external review and approval of all Laboratory related documentation.
Proactively progress documents through all stages to achieve schedule timelines and in accordance with site policies &amp;amp; in compliance with cGMP’s.
Be a reliable point of contact for the laboratory area for clear and precise communication of the documentation process and status of documents.
To co-ordinate processing of laboratory documents into and out-of ABB Documentation systems.
A key member on the laboratory readiness team during NPI, TT and routine Manufacturing, interfacing with all stakeholders to ensure the laboratory documents are prepared, executed and post approved in line with best practices and relevant timelines.
Ensure highest Quality &amp;amp; Compliance standards.
Track and trend relevant laboratory and business process metrics to ensure the laboratory are performing effectively and efficiently.
Perform all duties in accordance with GMP requirements, SOPs and controlled documents. • Support the generation of efficient, user friendly documentation including SOPs
Assist in the preparation of progress reports/presentations as required.
Revise, update, and format documentation including SOPs, forms, logbooks.
Write/review laboratory documentation (SOPs &amp;amp; Logbooks) ensuring it is current, accurate and in accordance with regulatory requirements.
Will act as an SME for the laboratory function and also the wider organization in adherence to GDP guidelines.
Will be flexible to take on additional tasks and responsibilities at the discretion of their manager.
Applies knowledge, experience, and technical skills to understand laboratory objectives, to provide support to laboratory initiatives, to execute processes and procedures efficiently and compliantly, evaluates documents for improvement potential.
Use standard practices to ensure inter-group consistency. Works, within established systems to improve Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) compliance across the laboratory department.
Schedules and execute tasks, with limited assistance, to support laboratory schedule timelines.
Circulates documents to reviewers and approvers with limited assistance, responds to comments and questions and coordinate referrals across the cross functional groups.
Manages document review and approval to meet schedule timelines.
Exercises judgment within generally defined procedures and practices to determine appropriate action.
Tracks ongoing problems and gathers information for analysis. Analyze data to develop solutions to general-level problems.
Presents a potential solution to management/senior personnel and with assistance creates an implementation plan.
Investigates Documentation related events in production that have quality or compliance impact.
Leads or participates IIA, RCI sessions.
Documents investigation outcomes.
Frequently interacts with functional peer groups. Interaction normally requires the ability to gain cooperation of others, conducting presentations of technical information concerning specific projects, schedules, etc.
Comply with policies and procedures, Standards and Specifications, Plant procedures, and regulatory agencies regulations and requirements.
Manage the laboratory Finite Schedule, including facilitating meetings, tracking adherence to schedule and KPI monitoring and reporting.

 
What you need to apply:

• Bachelor’s Degree or equivalent preferential, preferably in a Science or related field
Experience Level = 1+ Years
Experience in a regulated laboratory setting. 
Minimum of 1 year document control and records management experience in a regulated industry is strongly preferred. 
Expertise with Microsoft Word with a solid understanding of the review and formatting tools is required. 
Expertise with Outlook, Visio, Excel, PowerPoint is required. 
Expertise in proofing and editing controlled documents for spelling, grammar, formatting and cGMP compliance is required. 
Experience with the use of electronic systems to manage, edit and control documents is preferred.
A proven track record executing, reviewing and approving GMP documentation to the highest GDP Standards
Previous experience in a fast-paced and deadline driven environment is required
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[QC Analytical Analyst]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-19 10:03:53]]></date><referencenumber><![CDATA[1763]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1763&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QC Analytical Analyst for our client in Sligo.
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site.

 
What you will be doing:

Ensuring Analytical Laboratory Documentation and Computerized Systems compliance with Data Integrity policies and regulatory requirements.
Understanding Regulations and business processes required to maintain Laboratory Data Integrity.
Ensuring timely completion of all laboratory analysis assigned to shift.
Ensuring that analysts working in the assigned cell or team are performing to the best of their ability, coaching and providing guidance where issues occur such as poor set-up or test execution performance.
Improving the overall efficiency and velocity within the assigned team.
Identifying and implementing improvements in analytical practices using ‘Zero, Believe it, Achieve it’
Ensuring that the agreed test schedule is adhered to and identifying recovery paths to bring test schedules back into alignment with plant requirements.
Identifying weaknesses in laboratory performance and working with the laboratory management to rectify.
Supporting &amp;amp; initiating analytical OOS issues as they arise in a timely manner both through practical work and through the quality system.
Ensuring 5S excellence is maintained across the Laboratory.
Instilling a quality culture of Zero, Believe it, Achieve it amongst the laboratory team
Ensuring that all laboratory test equipment is utilised and maintained correctly.
Maintaining up-to-date, complete and precise records of all tests performed.
Investigates Documentation related events in production that have quality or compliance impact.
Leads or participates IIA, RCI sessions.
Documents investigation outcomes.
Frequently interacts with functional peer groups. Interaction normally requires the ability to gain cooperation of others, conducting presentations of technical information concerning specific projects, schedules, etc.
Comply with policies and procedures, Standards and Specifications, Plant procedures, and regulatory agencies regulations and requirements.

 
What you need to apply:

Bachelor’s Degree or equivalent preferential, preferably in a Science or related field
Experience Level = 1+ Years
Experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines
Proven track record in an analytical role. 
Proficient in using analytical equipment in a QC lab as well as troubleshooting.
Knowledgeable in instrumentation such as UHPLC, SoloVPE, TOC, and Identification techniques.
Experience in industry is essential.

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Planning Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-25 09:53:59]]></date><referencenumber><![CDATA[1766]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1766&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Planning Manager for a manufacturing facility based in the Connaught region. This role oversees and coordinates end-to-end supply chain planning processes, ensuring efficient production scheduling, inventory management, and material availability to support manufacturing operations while driving integration, risk management, and continuous improvement across the supply chain.
 
 
Why you should apply:

Join a company who strive to have a remarkable impact on people's lives across several key therapeutic areas – and are committed to operating with integrity.

 
What you will be doing:

Manage the monthly Sales &amp;amp; Operations Planning (S&amp;amp;OP) process and Long-Range Planning (LRP) process.
Create and oversee detailed production schedules, considering both demand and manufacturing capacity.
Foster and sustain productive working relationships with both internal teams and external partners to support collaboration and achieve organisational objectives.
Monitor and control inventory levels to ensure materials and products are available to meet production and customer needs, while reducing excess stock and related costs. 
Develop and analyse supply chain scenarios. 
Lead capacity planning and inventory management activities.
Support all planning functions, including Master Production Schedule (MPS) and Material Requirements Planning (MRP).
Track and report planning and operational performance metrics.
Participate in network-wide supply chain activities to enhance integration and service.
Drive and implement continuous improvement initiatives for planning processes.

 
What you need to apply:

Bachelor’s degree in a relevant technical or business field.  
Minimum of 6 years’ experience in manufacturing or supply chain environment, in a planning role.   Proficiency in MRP/ERP tools, especially SAP.  
Demonstrated leadership abilities.  
Effective communication and interpersonal skills, fostering collaboration across diverse functional teams.  
Commitment to adhering to safety, regulatory, and quality standards in all planning operations.
Proven problem-solving skills and the ability to develop and adapt strategies for changing business environment

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[Planning Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-25 09:53:59]]></date><referencenumber><![CDATA[1766-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1766&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Planning Manager for a manufacturing facility based in the Connaught region. This role oversees and coordinates end-to-end supply chain planning processes, ensuring efficient production scheduling, inventory management, and material availability to support manufacturing operations while driving integration, risk management, and continuous improvement across the supply chain.
 
 
Why you should apply:

Join a company who strive to have a remarkable impact on people's lives across several key therapeutic areas – and are committed to operating with integrity.

 
What you will be doing:

Manage the monthly Sales &amp;amp; Operations Planning (S&amp;amp;OP) process and Long-Range Planning (LRP) process.
Create and oversee detailed production schedules, considering both demand and manufacturing capacity.
Foster and sustain productive working relationships with both internal teams and external partners to support collaboration and achieve organisational objectives.
Monitor and control inventory levels to ensure materials and products are available to meet production and customer needs, while reducing excess stock and related costs. 
Develop and analyse supply chain scenarios. 
Lead capacity planning and inventory management activities.
Support all planning functions, including Master Production Schedule (MPS) and Material Requirements Planning (MRP).
Track and report planning and operational performance metrics.
Participate in network-wide supply chain activities to enhance integration and service.
Drive and implement continuous improvement initiatives for planning processes.

 
What you need to apply:

Bachelor’s degree in a relevant technical or business field.  
Minimum of 6 years’ experience in manufacturing or supply chain environment, in a planning role.   Proficiency in MRP/ERP tools, especially SAP.  
Demonstrated leadership abilities.  
Effective communication and interpersonal skills, fostering collaboration across diverse functional teams.  
Commitment to adhering to safety, regulatory, and quality standards in all planning operations.
Proven problem-solving skills and the ability to develop and adapt strategies for changing business environment

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[Planning Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-25 09:53:59]]></date><referencenumber><![CDATA[1766-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1766&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Planning Manager for a manufacturing facility based in the Connaught region. This role oversees and coordinates end-to-end supply chain planning processes, ensuring efficient production scheduling, inventory management, and material availability to support manufacturing operations while driving integration, risk management, and continuous improvement across the supply chain.
 
 
Why you should apply:

Join a company who strive to have a remarkable impact on people's lives across several key therapeutic areas – and are committed to operating with integrity.

 
What you will be doing:

Manage the monthly Sales &amp;amp; Operations Planning (S&amp;amp;OP) process and Long-Range Planning (LRP) process.
Create and oversee detailed production schedules, considering both demand and manufacturing capacity.
Foster and sustain productive working relationships with both internal teams and external partners to support collaboration and achieve organisational objectives.
Monitor and control inventory levels to ensure materials and products are available to meet production and customer needs, while reducing excess stock and related costs. 
Develop and analyse supply chain scenarios. 
Lead capacity planning and inventory management activities.
Support all planning functions, including Master Production Schedule (MPS) and Material Requirements Planning (MRP).
Track and report planning and operational performance metrics.
Participate in network-wide supply chain activities to enhance integration and service.
Drive and implement continuous improvement initiatives for planning processes.

 
What you need to apply:

Bachelor’s degree in a relevant technical or business field.  
Minimum of 6 years’ experience in manufacturing or supply chain environment, in a planning role.   Proficiency in MRP/ERP tools, especially SAP.  
Demonstrated leadership abilities.  
Effective communication and interpersonal skills, fostering collaboration across diverse functional teams.  
Commitment to adhering to safety, regulatory, and quality standards in all planning operations.
Proven problem-solving skills and the ability to develop and adapt strategies for changing business environment

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[Planning Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-25 09:53:59]]></date><referencenumber><![CDATA[1766-4]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1766&amp;Itemid=986]]></url><city><![CDATA[Leitrim]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Planning Manager for a manufacturing facility based in the Connaught region. This role oversees and coordinates end-to-end supply chain planning processes, ensuring efficient production scheduling, inventory management, and material availability to support manufacturing operations while driving integration, risk management, and continuous improvement across the supply chain.
 
 
Why you should apply:

Join a company who strive to have a remarkable impact on people's lives across several key therapeutic areas – and are committed to operating with integrity.

 
What you will be doing:

Manage the monthly Sales &amp;amp; Operations Planning (S&amp;amp;OP) process and Long-Range Planning (LRP) process.
Create and oversee detailed production schedules, considering both demand and manufacturing capacity.
Foster and sustain productive working relationships with both internal teams and external partners to support collaboration and achieve organisational objectives.
Monitor and control inventory levels to ensure materials and products are available to meet production and customer needs, while reducing excess stock and related costs. 
Develop and analyse supply chain scenarios. 
Lead capacity planning and inventory management activities.
Support all planning functions, including Master Production Schedule (MPS) and Material Requirements Planning (MRP).
Track and report planning and operational performance metrics.
Participate in network-wide supply chain activities to enhance integration and service.
Drive and implement continuous improvement initiatives for planning processes.

 
What you need to apply:

Bachelor’s degree in a relevant technical or business field.  
Minimum of 6 years’ experience in manufacturing or supply chain environment, in a planning role.   Proficiency in MRP/ERP tools, especially SAP.  
Demonstrated leadership abilities.  
Effective communication and interpersonal skills, fostering collaboration across diverse functional teams.  
Commitment to adhering to safety, regulatory, and quality standards in all planning operations.
Proven problem-solving skills and the ability to develop and adapt strategies for changing business environment

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[Planning Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-25 09:53:59]]></date><referencenumber><![CDATA[1766-5]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1766&amp;Itemid=986]]></url><city><![CDATA[Donegal]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Planning Manager for a manufacturing facility based in the Connaught region. This role oversees and coordinates end-to-end supply chain planning processes, ensuring efficient production scheduling, inventory management, and material availability to support manufacturing operations while driving integration, risk management, and continuous improvement across the supply chain.
 
 
Why you should apply:

Join a company who strive to have a remarkable impact on people's lives across several key therapeutic areas – and are committed to operating with integrity.

 
What you will be doing:

Manage the monthly Sales &amp;amp; Operations Planning (S&amp;amp;OP) process and Long-Range Planning (LRP) process.
Create and oversee detailed production schedules, considering both demand and manufacturing capacity.
Foster and sustain productive working relationships with both internal teams and external partners to support collaboration and achieve organisational objectives.
Monitor and control inventory levels to ensure materials and products are available to meet production and customer needs, while reducing excess stock and related costs. 
Develop and analyse supply chain scenarios. 
Lead capacity planning and inventory management activities.
Support all planning functions, including Master Production Schedule (MPS) and Material Requirements Planning (MRP).
Track and report planning and operational performance metrics.
Participate in network-wide supply chain activities to enhance integration and service.
Drive and implement continuous improvement initiatives for planning processes.

 
What you need to apply:

Bachelor’s degree in a relevant technical or business field.  
Minimum of 6 years’ experience in manufacturing or supply chain environment, in a planning role.   Proficiency in MRP/ERP tools, especially SAP.  
Demonstrated leadership abilities.  
Effective communication and interpersonal skills, fostering collaboration across diverse functional teams.  
Commitment to adhering to safety, regulatory, and quality standards in all planning operations.
Proven problem-solving skills and the ability to develop and adapt strategies for changing business environment

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[EM Senior Microbiologist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-26 11:02:41]]></date><referencenumber><![CDATA[1767]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1767&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QC Senior Micro for our client based in Dublin. This role will support manufacturing operations on a 24/7 shift pattern and may include extended hours
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Environmental Monitoring of Grade 8/9 Cleanrooms
 Environmental Monitoring of Grade 5/7 Cleanrooms &amp;amp; Isolator
Reading of Environmental Monitoring Plates
Bioburden testing of water &amp;amp; disinfectants
Writing technical reports
 Water sampling
Testing of In Process samples such as Density &amp;amp; pH
Technically strong background in microbiology and aseptic manufacturing
Experience in LIMS, Change Control, Trackwise, SAP and CDOCS an advantage
Flexibility – the EM role often encounters changing priorities on a daily basis
 Demonstrated leadership and communication skills
  Auditing documentation and operation process
Demonstrated ability to interact with regulatory agencies

 
What you need to apply:

Bachelors degree in a science discipline 
Biopharmaceutical QC experience in a microbiology lab 
Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products
Experience working in an aseptic cleanroom performing Environmental Monitoring
Proficient in the use of LIMS &amp;amp; LMES

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Senior Microbiologist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-26 11:04:18]]></date><referencenumber><![CDATA[1768]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1768&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QC Microbiology (Senior) for our client based in Dublin. The successful candidate would contribute to team by ensuring the quality of the tasks/services provided by self and contribute to the completion of milestones associated with specific projects or activities within team. 
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Endotoxin testing of water, in-process and drug product release samples
Bioburden testing of water &amp;amp; in-process drug product samples
Sterility testing
Water sampling
Lab Support duties such as Biological Indicator testing, Growth Promotion, Media Preparation,

Identifications and Autoclave.

Writing technical reports
Media fill reconciliation and inspection
Weekend bioburden cover
Perform analytical testing as a main priority with efficiency and accuracy
Report, evaluate, archive, trend and approve analytical dat
Troubleshoot, solve problems and communicate with stakeholders
Initiate and/or implement changes in controlled documents
Participate in audits, initiatives, and projects that may be departmental or organizational in scope
Write protocols and perform assay validation
Introduce new techniques to the lab, including method transfers, reports, validations and protocols.?

 
What you need to apply:

Bachelors degree in a science discipline
Biopharmaceutical QC experience in a microbiology lab?
Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products? 

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Opex Business Analyst]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-31 10:30:19]]></date><referencenumber><![CDATA[1771]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1771&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Opex Business Analyst
Team Horizon is seeking a Opex Business Analyst for a client in Cork. This person will be responsible for designing, developing, and maintaining digital dashboards that provide insights and data visualization to support business decision-making and performance improvements.
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site.

 What you will be doing:

Gathering requirements from stakeholders and understanding their data visualization needs.
Designing and developing interactive dashboards using company approved digital tools such as Power BI.
Creating data models and connecting to various data sources to extract and transform data.
Implementing data visualization best practices to present data in a clear and meaningful way including drill-throughs and analytical capabilities.
Collaborating with data analysts and business users to ensure the accuracy and relevance of the data displayed in the dashboards.
Optimizing dashboards for performance and usability.
Creating and publishing reports and dashboards to the Digital Tool such as Power BI for sharing with stakeholders.
Providing training and support to end-users on how to use and interpret the dashboards.

 What you need to apply:

18 month’s experience in one or more of the following: Basic C++, PowerApps, PowerBi, Power Automate, JSON, HTML, Dataverse, SQL Server, SharePoint, Relational Database Management
Experience with Visual Studio, Visual Studio Code, Power Platform CLI - JavaScript, TypeScript, React JS, Python Deliverables include, but are not limited to: - Metrics Dashboards - Balanced Scorecard Reports
Qualification Reports
 Automation usage statistics
 Integrated Survey and Reporting tool
 Training Delivery
Good understanding of data analysis and visualization principles, as well as strong problem-solving and communication skills.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[IT/Software]]></category></job><job><title><![CDATA[Talent Acquisition Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-14 16:59:19]]></date><referencenumber><![CDATA[1775]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1775&amp;Itemid=986]]></url><city><![CDATA[Mayo/Dublin/Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Are you a proactive recruiter who loves finding top talent in fast-paced environments? We’re looking for a Talent Acquisition Specialist to join our clients team and help shape the future of hiring in our organisation.
 
Why you should apply:

You’ll work in a dynamic, collaborative environment where your ideas are valued, your voice matters, and your expertise directly shapes the future of the organisation.
If you’re driven, curious, and ready for the next step, this role is where you can thrive

 
What you will be doing:

Recruitment will be focused on a specific team/function, or other areas as assigned.
Responsible for attracting top talent and developing a strong, qualified candidate pool for current and future openings.
Additional job duties include pre-screening candidates, project management, partnering with team members to develop sourcing strategies and providing talent for open positions.
Demonstrate ability to proactively identify, source and manage talent pools aligned to business priorities.
Core responsibility is to manage open job requisitions, update and manage SmartRecruiters, achieve recruiting metrics and report key accomplishments.
Will also compile and communicate the knowledge base, industry overviews, and market trends, data and analytics to team members and business leaders.
Will prepare and approve offer packages, providing equity &amp;amp; market competitiveness data research.
Ensure compliance to state/federal employment laws and policies and practices for applicant tracking compliance and reporting metrics.
Establish a true business partnership with hiring managers and leadership on all staffing related activities and issues.

 
What you need to apply:

Bachelor's degree required.
2-3+ years recruitment experience in a competitive, fast-paced environment required.
Must project a strong business presence and have the ability to instill confidence in clients and to deliver results.
Proactive recruiting and sourcing experience required.
Healthcare/Pharmaceutical industry recruitment experience strongly preferred.
Experience in managing requisitions within SmartRecruiters preferred.
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[Talent Acquisition Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-14 16:59:19]]></date><referencenumber><![CDATA[1775-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1775&amp;Itemid=986]]></url><city><![CDATA[Mayo/Dublin/Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Are you a proactive recruiter who loves finding top talent in fast-paced environments? We’re looking for a Talent Acquisition Specialist to join our clients team and help shape the future of hiring in our organisation.
 
Why you should apply:

You’ll work in a dynamic, collaborative environment where your ideas are valued, your voice matters, and your expertise directly shapes the future of the organisation.
If you’re driven, curious, and ready for the next step, this role is where you can thrive

 
What you will be doing:

Recruitment will be focused on a specific team/function, or other areas as assigned.
Responsible for attracting top talent and developing a strong, qualified candidate pool for current and future openings.
Additional job duties include pre-screening candidates, project management, partnering with team members to develop sourcing strategies and providing talent for open positions.
Demonstrate ability to proactively identify, source and manage talent pools aligned to business priorities.
Core responsibility is to manage open job requisitions, update and manage SmartRecruiters, achieve recruiting metrics and report key accomplishments.
Will also compile and communicate the knowledge base, industry overviews, and market trends, data and analytics to team members and business leaders.
Will prepare and approve offer packages, providing equity &amp;amp; market competitiveness data research.
Ensure compliance to state/federal employment laws and policies and practices for applicant tracking compliance and reporting metrics.
Establish a true business partnership with hiring managers and leadership on all staffing related activities and issues.

 
What you need to apply:

Bachelor's degree required.
2-3+ years recruitment experience in a competitive, fast-paced environment required.
Must project a strong business presence and have the ability to instill confidence in clients and to deliver results.
Proactive recruiting and sourcing experience required.
Healthcare/Pharmaceutical industry recruitment experience strongly preferred.
Experience in managing requisitions within SmartRecruiters preferred.
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[Talent Acquisition Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-14 16:59:19]]></date><referencenumber><![CDATA[1775-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1775&amp;Itemid=986]]></url><city><![CDATA[Mayo/Dublin/Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Are you a proactive recruiter who loves finding top talent in fast-paced environments? We’re looking for a Talent Acquisition Specialist to join our clients team and help shape the future of hiring in our organisation.
 
Why you should apply:

You’ll work in a dynamic, collaborative environment where your ideas are valued, your voice matters, and your expertise directly shapes the future of the organisation.
If you’re driven, curious, and ready for the next step, this role is where you can thrive

 
What you will be doing:

Recruitment will be focused on a specific team/function, or other areas as assigned.
Responsible for attracting top talent and developing a strong, qualified candidate pool for current and future openings.
Additional job duties include pre-screening candidates, project management, partnering with team members to develop sourcing strategies and providing talent for open positions.
Demonstrate ability to proactively identify, source and manage talent pools aligned to business priorities.
Core responsibility is to manage open job requisitions, update and manage SmartRecruiters, achieve recruiting metrics and report key accomplishments.
Will also compile and communicate the knowledge base, industry overviews, and market trends, data and analytics to team members and business leaders.
Will prepare and approve offer packages, providing equity &amp;amp; market competitiveness data research.
Ensure compliance to state/federal employment laws and policies and practices for applicant tracking compliance and reporting metrics.
Establish a true business partnership with hiring managers and leadership on all staffing related activities and issues.

 
What you need to apply:

Bachelor's degree required.
2-3+ years recruitment experience in a competitive, fast-paced environment required.
Must project a strong business presence and have the ability to instill confidence in clients and to deliver results.
Proactive recruiting and sourcing experience required.
Healthcare/Pharmaceutical industry recruitment experience strongly preferred.
Experience in managing requisitions within SmartRecruiters preferred.
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[Senior Product QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-16 17:25:43]]></date><referencenumber><![CDATA[1777]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1777&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Product QA Manager &amp;amp; QP to join our client’s team. This is a leadership role and is responsible for compliance with marketing authorisations, current Good Manufacturing Practices (GMP), and supporting New Product Introductions (NPIs).
 
 
Why you should apply:

This is an excellent opportunity to make an impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience.

 
 
What you will be doing:

Manage QP , Regulatory, Change Management and New Product Introduction teams, including annual goal setting, performance reviews, development, and talent management.
Ensure products (commercial and NPI/CTS) are manufactured and released in line with marketing authorisation, GMP, and company quality systems.
Lead batch review and release, documentation, checks, and test completion.
Oversee validation of manufacturing and testing processes and accurate record keeping.
Provide quality governance on deviations, planned changes, and exception reporting with proper authorisations and regulatory notifications.
Support NPI activities: change plan review, validation, documentation approval, and release of CTS batches
Execute regulatory requests and submissions, engage directly with regulatory agencies (FDA, HPRA).
Chair Change Review Boards, approve changes, oversee completion of QA tasks.
Conduct internal/external audits and participate in regulatory/customer inspections.
Manage complaint investigations, coordinate product recalls, and address quality defects.
Ensure compliance with FDA CFR Parts 210/211/Q7, EU GMPs (ICH Q7, Volume 4), and  QA Policies.
Review and approve Product Quality Reviews (PQRs) and track finished product data.
Provide QP oversight for SAP, LIMS setup changes, and manage site quality metrics.
Act as Designee for the Quality Director when required.
Lead department/site goals, provide technical leadership/guidance on QP/regulatory matters, and present technical data for decision-making.

 
What you need to apply:

MSc in Industrial Pharmaceutical Science (or a comparable course recognized for QP status per Article 49 of Directive 2001/83/EC).
Minimum 10 years' experience in the healthcare/pharma sector within FDA/EMA approved environments.
Demonstrated experience leading teams, with 7+ years in leadership roles Demonstrated attention to detail, strong problem-solving and innovative thinking abilities.
Results-driven mindset with proven prioritization skills and commitment to quality.
High integrity, strong work ethic, excellent verbal/written communication, and interpersonal skills.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Senior Product QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-16 17:25:43]]></date><referencenumber><![CDATA[1777-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1777&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Product QA Manager &amp;amp; QP to join our client’s team. This is a leadership role and is responsible for compliance with marketing authorisations, current Good Manufacturing Practices (GMP), and supporting New Product Introductions (NPIs).
 
 
Why you should apply:

This is an excellent opportunity to make an impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience.

 
 
What you will be doing:

Manage QP , Regulatory, Change Management and New Product Introduction teams, including annual goal setting, performance reviews, development, and talent management.
Ensure products (commercial and NPI/CTS) are manufactured and released in line with marketing authorisation, GMP, and company quality systems.
Lead batch review and release, documentation, checks, and test completion.
Oversee validation of manufacturing and testing processes and accurate record keeping.
Provide quality governance on deviations, planned changes, and exception reporting with proper authorisations and regulatory notifications.
Support NPI activities: change plan review, validation, documentation approval, and release of CTS batches
Execute regulatory requests and submissions, engage directly with regulatory agencies (FDA, HPRA).
Chair Change Review Boards, approve changes, oversee completion of QA tasks.
Conduct internal/external audits and participate in regulatory/customer inspections.
Manage complaint investigations, coordinate product recalls, and address quality defects.
Ensure compliance with FDA CFR Parts 210/211/Q7, EU GMPs (ICH Q7, Volume 4), and  QA Policies.
Review and approve Product Quality Reviews (PQRs) and track finished product data.
Provide QP oversight for SAP, LIMS setup changes, and manage site quality metrics.
Act as Designee for the Quality Director when required.
Lead department/site goals, provide technical leadership/guidance on QP/regulatory matters, and present technical data for decision-making.

 
What you need to apply:

MSc in Industrial Pharmaceutical Science (or a comparable course recognized for QP status per Article 49 of Directive 2001/83/EC).
Minimum 10 years' experience in the healthcare/pharma sector within FDA/EMA approved environments.
Demonstrated experience leading teams, with 7+ years in leadership roles Demonstrated attention to detail, strong problem-solving and innovative thinking abilities.
Results-driven mindset with proven prioritization skills and commitment to quality.
High integrity, strong work ethic, excellent verbal/written communication, and interpersonal skills.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Senior Product QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-16 17:25:43]]></date><referencenumber><![CDATA[1777-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1777&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Product QA Manager &amp;amp; QP to join our client’s team. This is a leadership role and is responsible for compliance with marketing authorisations, current Good Manufacturing Practices (GMP), and supporting New Product Introductions (NPIs).
 
 
Why you should apply:

This is an excellent opportunity to make an impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience.

 
 
What you will be doing:

Manage QP , Regulatory, Change Management and New Product Introduction teams, including annual goal setting, performance reviews, development, and talent management.
Ensure products (commercial and NPI/CTS) are manufactured and released in line with marketing authorisation, GMP, and company quality systems.
Lead batch review and release, documentation, checks, and test completion.
Oversee validation of manufacturing and testing processes and accurate record keeping.
Provide quality governance on deviations, planned changes, and exception reporting with proper authorisations and regulatory notifications.
Support NPI activities: change plan review, validation, documentation approval, and release of CTS batches
Execute regulatory requests and submissions, engage directly with regulatory agencies (FDA, HPRA).
Chair Change Review Boards, approve changes, oversee completion of QA tasks.
Conduct internal/external audits and participate in regulatory/customer inspections.
Manage complaint investigations, coordinate product recalls, and address quality defects.
Ensure compliance with FDA CFR Parts 210/211/Q7, EU GMPs (ICH Q7, Volume 4), and  QA Policies.
Review and approve Product Quality Reviews (PQRs) and track finished product data.
Provide QP oversight for SAP, LIMS setup changes, and manage site quality metrics.
Act as Designee for the Quality Director when required.
Lead department/site goals, provide technical leadership/guidance on QP/regulatory matters, and present technical data for decision-making.

 
What you need to apply:

MSc in Industrial Pharmaceutical Science (or a comparable course recognized for QP status per Article 49 of Directive 2001/83/EC).
Minimum 10 years' experience in the healthcare/pharma sector within FDA/EMA approved environments.
Demonstrated experience leading teams, with 7+ years in leadership roles Demonstrated attention to detail, strong problem-solving and innovative thinking abilities.
Results-driven mindset with proven prioritization skills and commitment to quality.
High integrity, strong work ethic, excellent verbal/written communication, and interpersonal skills.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Senior Product QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-16 17:25:43]]></date><referencenumber><![CDATA[1777-4]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1777&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Product QA Manager &amp;amp; QP to join our client’s team. This is a leadership role and is responsible for compliance with marketing authorisations, current Good Manufacturing Practices (GMP), and supporting New Product Introductions (NPIs).
 
 
Why you should apply:

This is an excellent opportunity to make an impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience.

 
 
What you will be doing:

Manage QP , Regulatory, Change Management and New Product Introduction teams, including annual goal setting, performance reviews, development, and talent management.
Ensure products (commercial and NPI/CTS) are manufactured and released in line with marketing authorisation, GMP, and company quality systems.
Lead batch review and release, documentation, checks, and test completion.
Oversee validation of manufacturing and testing processes and accurate record keeping.
Provide quality governance on deviations, planned changes, and exception reporting with proper authorisations and regulatory notifications.
Support NPI activities: change plan review, validation, documentation approval, and release of CTS batches
Execute regulatory requests and submissions, engage directly with regulatory agencies (FDA, HPRA).
Chair Change Review Boards, approve changes, oversee completion of QA tasks.
Conduct internal/external audits and participate in regulatory/customer inspections.
Manage complaint investigations, coordinate product recalls, and address quality defects.
Ensure compliance with FDA CFR Parts 210/211/Q7, EU GMPs (ICH Q7, Volume 4), and  QA Policies.
Review and approve Product Quality Reviews (PQRs) and track finished product data.
Provide QP oversight for SAP, LIMS setup changes, and manage site quality metrics.
Act as Designee for the Quality Director when required.
Lead department/site goals, provide technical leadership/guidance on QP/regulatory matters, and present technical data for decision-making.

 
What you need to apply:

MSc in Industrial Pharmaceutical Science (or a comparable course recognized for QP status per Article 49 of Directive 2001/83/EC).
Minimum 10 years' experience in the healthcare/pharma sector within FDA/EMA approved environments.
Demonstrated experience leading teams, with 7+ years in leadership roles Demonstrated attention to detail, strong problem-solving and innovative thinking abilities.
Results-driven mindset with proven prioritization skills and commitment to quality.
High integrity, strong work ethic, excellent verbal/written communication, and interpersonal skills.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Senior Product QA Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-16 17:25:43]]></date><referencenumber><![CDATA[1777-5]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1777&amp;Itemid=986]]></url><city><![CDATA[Leitrim]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Product QA Manager &amp;amp; QP to join our client’s team. This is a leadership role and is responsible for compliance with marketing authorisations, current Good Manufacturing Practices (GMP), and supporting New Product Introductions (NPIs).
 
 
Why you should apply:

This is an excellent opportunity to make an impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience.

 
 
What you will be doing:

Manage QP , Regulatory, Change Management and New Product Introduction teams, including annual goal setting, performance reviews, development, and talent management.
Ensure products (commercial and NPI/CTS) are manufactured and released in line with marketing authorisation, GMP, and company quality systems.
Lead batch review and release, documentation, checks, and test completion.
Oversee validation of manufacturing and testing processes and accurate record keeping.
Provide quality governance on deviations, planned changes, and exception reporting with proper authorisations and regulatory notifications.
Support NPI activities: change plan review, validation, documentation approval, and release of CTS batches
Execute regulatory requests and submissions, engage directly with regulatory agencies (FDA, HPRA).
Chair Change Review Boards, approve changes, oversee completion of QA tasks.
Conduct internal/external audits and participate in regulatory/customer inspections.
Manage complaint investigations, coordinate product recalls, and address quality defects.
Ensure compliance with FDA CFR Parts 210/211/Q7, EU GMPs (ICH Q7, Volume 4), and  QA Policies.
Review and approve Product Quality Reviews (PQRs) and track finished product data.
Provide QP oversight for SAP, LIMS setup changes, and manage site quality metrics.
Act as Designee for the Quality Director when required.
Lead department/site goals, provide technical leadership/guidance on QP/regulatory matters, and present technical data for decision-making.

 
What you need to apply:

MSc in Industrial Pharmaceutical Science (or a comparable course recognized for QP status per Article 49 of Directive 2001/83/EC).
Minimum 10 years' experience in the healthcare/pharma sector within FDA/EMA approved environments.
Demonstrated experience leading teams, with 7+ years in leadership roles Demonstrated attention to detail, strong problem-solving and innovative thinking abilities.
Results-driven mindset with proven prioritization skills and commitment to quality.
High integrity, strong work ethic, excellent verbal/written communication, and interpersonal skills.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Project Engineer (Syringe Inspection)]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-21 12:12:30]]></date><referencenumber><![CDATA[1778]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1778&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Project Engineer (Syringe Inspection)
Team Horizon is seeking a Project Engineer (Syringe Inspection) for a client in Dublin who will support the installation, validation, and lifecycle management of automated syringe inspection systems within a GMP fill-finish facility expansion.
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Act as System Owner (SO) for automated syringe inspection systems.
SO during the FAT/SAT, commissioning, qualification, and validation activities.
Ensure compliance with GMP, Annex 1, and data integrity requirements.
Own system performance metrics including: False reject rates, Detection capability, OEE performance
Support inspection recipe development and optimisation.
Develop maintenance and lifecycle strategies for inspection equipment.
Lead troubleshooting and root cause investigations for inspection failures.
Support audit readiness and regulatory inspections.

What you need to apply:

Bachelor’s Degree in Engineering (Mechanical, Electrical, Automation, or related discipline).
5+ years’ experience in biopharmaceutical manufacturing.
Experience with Automated visual inspection systems (AVI), Vision systems, High-speed packaging or inspection lines
Understanding of particulate detection, cosmetic defect inspection, and container closure integrity.
Experience supporting equipment validation and data integrity compliance.
Strong analytical and problem-solving skills.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Process Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-21 14:57:10]]></date><referencenumber><![CDATA[1779]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1779&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Process Engineer (Senior)
Team Horizon is seeking a Process Engineer (Senior) for a client in Dublin who will provide technical support to large molecule and small molecule drug product manufacturing as well as part of the global Process Development (PD) organization. 
 Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Developing single use systems in collaboration with site teams and network for DP formulation and filling.
Authoring / verification of single use qualification packages.
Filling characterisation support (Filling recipe development - protocol development / execution and reporting.) 
Demonstrated ability in providing leadership to cross-functional teams to advance complex projects to completion. Excellent Communication skills are essential for this role, as well as a demonstrated proficiency with the principles of Technical Writing.
Leads and conducts risk assessment for drug product operations and propose / implement appropriate CAPA.
Provide process development expertise for drug product processing in specific areas such as sterile processing, process characterization, filling, SUS. Support commercial drug product manufacturing operations with technical evaluation of NC/CAPA and technology transfer. Interfaces with manufacturing as well as all support functions to provide robust and coordinated support to manufacturing.
Troubleshoots issues with drug product processing technologies and equipment. Champions use of data-driven analyses and visualizations. Investigates to determine root cause.
Lead or assist in deviation / exception resolution and root cause analysis.
Responsibilities may include leading cross-site teams to support the above activities, providing recommendations to management.
Ensure that the site meets the quality requirements of its customers and applicable regulations (FDA, EU &amp;amp; international standards).
Review and post-approve process validation protocols and assessments from a quality system documentation perspective.
Contribute to product quality assessments and process flow documents.
Liaise with Operations, Engineering and external vendors regarding new or amended equipment which would impact the validated process.

What you need to apply:
Basic Qualifications:       

A third level Bachelor’s Degree in Science, Engineering or a relevant Quality discipline with 5 years’ experience in a similar role OR Master’s degree &amp;amp; 3 years of directly related experience OR Associate’s degree &amp;amp; 10 years of directly related experience.
Knowledge of cGMPs and other worldwide regulatory requirements.
Thorough knowledge of aseptic manufacturing technologies and cGMP.
Problem solving ability and excellent oral and written communications skills
Strong skills in applying fundamental engineering and scientific principles to the design and implementation of Formulation Single use systems and Filling.

Preferred Qualifications: 

10 + years of experience in support of Commercial Protein Drug Product (DP) processing in specific areas such as Sterile Processing, Process Characterization, Tech Transfer (to commercial DP sites) or Validation.
Strong skills in applying fundamental engineering and scientific principles to the design, implementation and process validation of formulation, mixing, filtration and filling.  Knowledge of protein biochemistry regarding chemical and physical stability
Background in Drug product Filling technologies, Peristaltic pumping / Time pressure filling.   
Strong knowledge of Quality systems, Drug Product Manufacturing and Validation.
Demonstrated ability in providing leadership to cross-functional teams to advance complex projects to completion. Excellent Communication skill is essential for this role.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[MES Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-22 11:29:40]]></date><referencenumber><![CDATA[1780]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1780&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[MES Engineer
Team Horizon is seeking a MES Engineer for a pharmaceutical client in Sligo. This person will be supporting multiple projects within MES across Medical Device and Biologics divisions. 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Support SAP and MES strategy.
Continuously review and manage business risk associated with POMSnet system and recipes. Continuously review and ensure all business processes, including SOPs, required to implement and manage SAP and POMSnet system changes and POMSnet recipe changes comply with current Safety, Quality and Information Technology policies.
Continuously review and ensure all documented policies, procedures and training plans required to implement and manage SAP and POMSnet system changes and POMSnet recipe changes comply with current Safety, Quality and Information Technology requirements.
Ensure the timely and compliant qualification of POMSnet recipes and upgrades aligned with business objectives.
Support SAP business system as local key user (LKU) for POMSnet and material queries.
Communicates project status by preparing standard status reports, and by participating in departmental and customer project status update meetings.
 Resolves project/system/ recipe issues by working with team members, project customers, and others as appropriate.
Responsible for systems compliance with quality related SOP’s.
Promote a culture of perfect performance and right first time within their team.
Required to front audits by HPRA/FDA or Customers on SAP and MES.
Participate in MES knowledge exchange with MES and other sites
Participate in MES Technical Review Board (TRB) Meetings, and manage issues, workarounds and fixes identified.
Participate in projects from initiation to ensure MES system or hardware requirements are understood and taken into consideration.

What you need to apply:

Demonstrated working knowledge of Manufacturing Execution Systems is required for this role.
Relevant science/engineering or IT discipline OR Degree Relevant science/engineering or IT discipline
A minimum of three years’ experience in an FDA/ HPRA regulated industry.
A strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
A good knowledge of the POMSnet or other MES system is required for this role.
Experience of operating in a team environment with active participation in proactive improvement programs is required. 
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Quantity Surveyor Advisor]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-05 10:39:40]]></date><referencenumber><![CDATA[1784]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1784&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Quantity Surveyor Advisor
Team Horizon is seeking a Quantity Surveyor Advisor in Dublin. The purpose of this role is to provide professional advice supporting the preparation, management, and delivery of the health capital program
They will also provide professional advice on all aspects of procurement, contract, and commercial related issues which related to the delivery of capital projects.
 Why you should apply:

You will join an innovative team, working among a diverse group of visionaries, thinkers and doers, working on developing pioneering solutions that lead to shared success.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 What you will be doing:

Assist with the delivery of the Capital plan for the area in compliance with Capital Approval Protocols, Public Procurement requirements and the financial Regulations.
Preparation of Capital submissions in accordance with Capital Approval protocols and Infrastructure Guideline requirements.
Provide support and advice in strategic planning, briefing, construction, equipping and related matters
Assist with the application of the Infrastructure Guidelines and the various requirements as set out in Guidelines at each of the Project Lifecycle stages as defined in the Infrastructure Guidelines to ensure value for money, the evaluation, planning and management of public investment projects.
Provide all relevant procurement, contractual and commercial advice required to deliver the various capital projects being delivered within the area.
Developing action plans for the timely and efficient completion of contracts. Co- ordinating the tender and control stages of projects, having close liaison with design teams, site supervisory staff, etc. on the one hand and hospital personnel on the other.
Managing the necessary and appropriate consultation processes, meetings, and other activities necessary to satisfactory completion of the project.
Managing the necessary and appropriate consultation processes, meetings, and other activities necessary to satisfactory completion of the project.
Complying with all regulatory and statutory requirements including permission, licences, certificates, and approvals.
Ensure all works are carried out in compliance with Health and Safety regulations.
Supervising staff and contractors in the implementation of agreed programmes.
Assist in the management of projects and helping to quickly resolve such issues as may be for resolution and agreement.
Managing the processing, certification and controlling expenditure on each assigned project. This is to include presentations to the Principal Quantity Surveying Adviser and the local Capital &amp;amp; Estates teams as required, of information and current estimates of total costs, running statements of financial commitment and forecasts of expenditure
Defining requirements for design services, buildings, and equipment.
Procurement and selection of Design Teams, other professional services, and contractors for Capital Projects, arranging and managing the procurement processes.
Obtaining approval to proposals as necessary in accordance with protocols and regulations in a timely manner.
Developing proposals with selected design teams and contractors.
Health estate planning, option studies, briefing, design development and project management with a view to optimising value related to best outcomes.

What you need to apply:

Hold a Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) major academic award in Quantity Surveying accredited by the relevant Professional Institute (Society of Chartered Surveyors in Ireland, Royal Institution of Chartered Surveyors).
Be registered as a Quantity Surveyor or be eligible for registration as a Quantity Surveyor under the Building Control Act 2007. Have a full membership of or be eligible for membership of a relevant professional association.
Have had at least 7 years’ satisfactory &amp;amp; relevant experience fulfilling the role of a Quantity Surveyor within either a contractor organisation or a private consultancy business.
Candidates must possess the requisite knowledge and ability (including a high standard of suitability and of administrative capacity) for the proper discharge of the duties of the office.  
Membership of the relevant professional association:  Society of Chartered Surveyors in Ireland / Royal Institution of Chartered Surveyors 
Candidates should have full, professional membership i.e. be a chartered member of the Society of Chartered Surveyors in Ireland and or Royal Institute Chartered Surveyors (Quantity Surveying)    
Good Knowledge and Experience of the design and construction and maintenance requirements of buildings and building services.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Quality Control Talent ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-07 15:30:16]]></date><referencenumber><![CDATA[1787]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1787&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[We are seeking scientific talent across Chemistry, Microbiology, Bioassay, and Analytical disciplines to support GMP-regulated pharmaceutical operations. All work is conducted in compliance with EU GMP / FDA standards, with strong emphasis on data integrity, scientific rigor, and patient safety.
This QC framework defines the working standards candidates will operate within.
Scientific Disciplines in Scope
1. Analytical Chemistry / QC Chemistry

HPLC / UPLC assay &amp;amp; impurity testing
GC analysis (residual solvents)
Dissolution testing
Karl Fischer / moisture content
Method verification and transfer support
Stability testing (ICH conditions)

2. Microbiology / Environmental Monitoring

Bioburden and microbial limit testing
Sterility testing (where applicable)
Endotoxin testing (LAL)
Environmental monitoring (viable &amp;amp; non-viable)
Water system monitoring (PW/WFI)
Media preparation and growth promotion testing

3. Bioassay / Cell-Based Testing

Cell culture maintenance and aseptic handling
Potency assays (in vitro bioactivity testing)
ELISA / ligand-binding assays
Reference standard qualification support
Assay validation and trending
Data analysis and variability control

4. Analytical / Data &amp;amp; Instrumentation Support

Instrument calibration verification
System suitability testing
Chromatography data review (CDS systems e.g. Empower)
Audit trail review and data integrity checks
Method troubleshooting and optimization support
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Reliability Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-11 16:39:31]]></date><referencenumber><![CDATA[1788]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1788&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Reliability Engineer
Team Horizon is seeking a Reliability Engineer for a client in Mayo who will be supporting the Maintenance Excellence Program (MEP) through advanced reliability engineering methods. 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Develop a reliability road map for own business unit and receive endorsement from the Senior Leadership Team.
Drive reliability culture by leading Reliability Centred Maintenance, Root Cause Analysis, Preventive Maintenance Optimisation and Reliability Improvement Project initiatives.
Evaluate and expand the predictive maintenance program to identify and prevent emerging failures and maintain a rolling yearly log of cost savings.
Analyse highly automated machinery to generate a top 10 bad actor profile and identify, execute and report on actions taken for the top 3 high value detractors.
Link actions to financial benefit and align priorities with the largest opportunities for the business.
Build strong relationships with Global Engineering and local engineering and maintenance teams.
Be a key contributor in the reliability engineering community of practice and smart maintenance initiatives.
Ensure compliance with policies, procedures and regulatory standards. Champion good EHS practices and support the site safety culture

What you need to apply:

Third-level qualification in Engineering.
3+ years experience within a regulated and/or highly automated environment. Strong data analytics skills.
Reliability engineering and continuous improvement experience and/or certification desirable. (Green belt and/or CMRP or CRL preferred).
Demonstrated ability to analyse machinery, conceptualise, implement and quantify significant improvements in OEE.
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Validation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-11 16:42:52]]></date><referencenumber><![CDATA[1789]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1789&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Validation Engineer for our client’s Technical Operations team in the Northwest. This is a fixed term contract for 12 months and will report to the Validation Team Lead.
 
 
Why you should apply:

This role will provide you the opportunity to get exposure to a broad range of validation activities on site, and you
You will be responsible for co-ordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements.

What you will be doing:

Co-ordinate, implement and participate in the site Validation Program.
Ensure all computerised systems are qualified in compliance with Data Integrity policies and regulatory requirements.
Co-ordinate / direction and participate in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
Generate/maintain Validation Master Plans.
Generate /maintain Project Validation Plans.
Generate validation plans, write protocols and final reports to cGMP standard.
Review / approve of protocols and final reports as required.
Manage validation change control process.
Adhere to and support all EHS &amp;amp; E standards, procedures and policies.

 
What you need to apply:

3rd level qualification in a relevant engineering or scientific discipline.
A minimum of 2 years’ experience in a cGMP regulated pharmaceutical manufacturing environment.
High level of attention to detail and mental concentration, to ensure accuracy and compliance. Excellent communications skills with the ability to write protocols and reports. 
Proven problem-solving skills and the ability to adapt to new regulatory requirements.

 
 ]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Senior Quality Specialist NPI ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-12 12:29:09]]></date><referencenumber><![CDATA[1790]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1790&amp;Itemid=986]]></url><city><![CDATA[Dublin / Hybrid ]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Quality Specialist on an initial 12-month contract. 
This key role must ensure effective interaction with other departments and locations regarding GMP Document review and finished product releases. This will involve partnering with major stakeholders such as Manufacturing, QC, QPs, Technical services, Engineering and Planning to optimize patient supply.
 
 
Why you should apply:

Join a team who unleash bold thinking with the power to inspire life-changing medicines.
Hybrid role with a mix of in-person working to give a platform to connect, work at pace and challenge perceptions with balance of remote working 2 days per week.

 
What you will be doing:

Quality Oversight for new product introduction in Bulk Drug Substance facility.
Quality oversight for new or modified facilities, equipment, technologies, including analytical, as well as other continuous improvements and requalification’s.
Site QA responsibility to provide technical expertise for all QA and compliance topics / issues relating manufacturing
Review and Approve project documents involving cross-functional, multi-departmental teams including: Operations, Process Engineering, Quality Control, Quality Assurance, Facilities, Equipment and others.
Review and approval of qualification/verification/validation documents for facilities, equipment, processes, analytical methods, suppliers, software and others. (e.g. URS, Facility, Utility, IT Systems, Test Methods, and Equipment validations) to ensure compliance with current regulatory expectations, EU, FDA and Corporate Standards and Internal Procedures.
Quality oversight on operations and technical services to review and approve Process descriptions , sampling plans, operational procedures, process validation and cleaning validation documents
Review and Approve TRA’s, MSRs, SAP requests related to new products .
Provide QA support for supplier qualifications.
QA review all analytical facility, equipment and method qualifications and validations.
Ensure all Materials are sampled and released as per the approved specifications and procedures .
Investigation and approval of deviations generated encountered during qualification/validation testing.
Participation in the project change control program and deviations for modifications to new and existing systems. equipment.
Provide guidance to project teams on Quality regulations for Validation strategy and approach.
Performs timely review of documentation/investigations/reports highlighting and assisting in the resolution of issues commensurate with the level of risk
Ensures schedules for review and approval of GMP documents are maintained to meet the needs of Commercial Operations groups.
Provide sound QA and Compliance support to manufacturing, engineering, automation, utilities, supply chain, and material movement and laboratories.
Provide support for deviation investigations, including root cause analysis, and corrective &amp;amp; preventative action (CAPAs) proposals and initiatives.
Actively support audit readiness activities and regulatory agency and internal audits.

 
What you need to apply:

Third level qualification e.g. B.Sc. in science/pharmacy or equivalent with a minimum of 6-8 years’ experience in cGMP Quality environment
Experience of sterility assurance for drug products and in manufacturing processes for pharmaceutical products and processes strongly desirable.
Direct experience of GMP management within a pharma/biopharma company is essential, and will include exposure to FDA, HPRA/EMA or other authorities of similar standing.
Excellent accuracy and attention to detail
Good knowledge of relevant computer packages e.g. Delta-V, Veeva vault or similar
Planning and organizing skills are required to plan, execute and track commitments of Quality Assurance and to adjust to changing priorities.
High level technical skills including analytical, auditing, pharmaceutical manufacturing and regulatory inspection management.
Previous QA experience aligned to Technical Services, Engineering/CQV reviews, operational (batch records, procedures), supplier qualification, packaging lines, warehousing (including temperature mapping of, along with fridges and freezers) and QC analytical qualifications/validations and laboratories of particular interest.
Excellent interpersonal skills are required, as is the ability to communicate well, both verbally and written
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Operational Readiness Sr Associate ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-14 14:17:42]]></date><referencenumber><![CDATA[1791]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1791&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Operational Readiness Sr Associate
Team Horizon is seeking an Operational Readiness Sr Associate for a client in Dublin who will be responsible for ensuring operational readiness by supporting cross-functional execution across all major milestones.
The person in this role will enable day-to-day execution by coordinating inputs across Manufacturing, Quality, Engineering, EHS and other stakeholders, ensuring dependencies are understood, decisions are actioned, and readiness activities remain on track. The Operational Readiness Sr. Associate will monitor compliance and adherence metrics.
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Support operational readiness planning and execution across all key milestones.
 Maintain a forward-looking view of execution needs (12–18 months) to ensure equipment, commissioning, qualification and manufacturing preparedness activities are sequenced to enable safe start-up and reliable operations.
Align Manufacturing, Quality, Engineering, EHS and other functional readiness plans into a single execution rhythm, ensuring handoffs, constraints and critical dependencies are understood and actively managed.
Provide clear visibility of readiness status, identify operational risks and escalate emerging issues to maintain compliance, safety and reliability.
Establish consistent ways of working for readiness reviews, decision logging and action closure to keep teams aligned and accountable.
Establish and enforce structured progress tracking mechanisms across all workstreams.
Ensure timely updates from functional teams and validate accuracy of reported progress, track milestone readiness and ensure alignment with overall project timelines. Hold teams to account through identifying performance gaps and drive accountability with stakeholders.
Support regular reporting cycles with accurate, data-driven insights, proactively identify schedule risks, bottlenecks, and dependency conflicts.
Escalate risks that could impact critical milestones such as Media Fill or PPQ and should partner with stakeholders to define mitigation plans and track resolution.
Ensure all functions are aligned to a single integrated schedule and planning framework and act as a central coordination point for schedule-related decision-making.

What you need to apply:

Strong understanding of project lifecycle phases (commissioning, qualification, etc.).
Ability to manage complex, cross-functional dependencies.
Strong analytical and problem-solving skills.
Excellent stakeholder management and communication skills.
AI mindset
Prior Manufacturing experience or relevant experience in pharma/biotech or large-scale project environments preferred.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Commissioning Lead ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-18 15:12:18]]></date><referencenumber><![CDATA[1792]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1792&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Commissioning Lead
 
Team Horizon is seeking a Commissioning Lead in Dublin. The Equipping and Commissioning Lead will be responsible for coordinating and providing a range of clinical and non-clinical equipping services, and advice in the context of delivering a fully integrated sourcing and logistics service for the project. 
Why you should apply:

You enjoy working in a culture of learning and collaboration and making a positive impact.
Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.

What you will be doing:

Lead equipping and commissioning activities for the programme workstream.
Develop and implement equipment procurement and commissioning strategies.
Coordinate equipment specifications, procurement evaluations, and contract awards.
Drive value-for-money initiatives and cost-saving opportunities.
Align procurement activities across multiple workstreams and stakeholders.
Manage risks, assumptions, issues, and dependencies (RAID).
Support readiness assessments and Go/No-Go commissioning decisions.
Ensure compliance with health &amp;amp; safety, and sustainability standards.
Work collaboratively with internal teams, contractors, and external stakeholders.

What you need to apply:
Essential Requirements: 

Level 8+ qualification in Architecture, Engineering, or Surveying accredited by a recognised professional body, or full professional membership (Engineers Ireland, RIAI, SCSI, RICS).
Proven experience managing procurement and commissioning on large, complex projects.
Strong knowledge of project management, procurement, construction, and building services.
Understanding of healthcare environments, HIQA standards, and public procurement processes.
Experience in risk management, reporting, budgeting, and stakeholder management.
Excellent communication, leadership, planning, and organisational skills.

Preferred Skills

Knowledge of healthcare facility design, maintenance, and compliance standards.
Professional project management certification (PRINCE2, CAPM, or equivalent) desirable
Ability to manage multidisciplinary teams and deliver results in fast-changing environments.
Strong problem-solving, negotiation, and decision-making abilities.
High proficiency in Microsoft Office, ICT systems, and report writing.

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Validation Engineer Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-28 09:44:38]]></date><referencenumber><![CDATA[1794]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1794&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a contract Validation Engineer for our clients aseptic manufacturing facility in the Connaught region.
 
Why you should apply:

This role will provide you the opportunity to get exposure to a broad range of validation activities on site, and you
You will be responsible for co-ordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements.

What you will be doing:

Active participation in the Site Validation Program and general Quality Assurance activities.
Coordination / direction and active participation in the validation and qualification of ABB equipment, utilities, processes and software in compliance with AbbVie policies, FDA, European cGMP and GAMP
standards.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards. QA support for validation investigations and implementation of corrective actions.
Vendor supervision for execution of validation activities.
Execution of Autoclave, Parts washer, Lyo, CIP and SIP ,  VHP and Temperature Mapping  to meet initial validation and revalidation requirements.
Creation/Review/Approval of various validation and qualification documents
Management of validation, exception event, and change control
processes.
Documenting all activities in line with cGMP requirements.
Performing cross training within the team and training of new team
members.
Participation in continuous improvement programs to implement
improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team
members.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Relevant degree and 5 years’ experience
Autoclave validation execution experience
Aseptic processing validation including media fills and VHP validation execution
HVAC validation

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineer Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-28 09:44:38]]></date><referencenumber><![CDATA[1794-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1794&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a contract Validation Engineer for our clients aseptic manufacturing facility in the Connaught region.
 
Why you should apply:

This role will provide you the opportunity to get exposure to a broad range of validation activities on site, and you
You will be responsible for co-ordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements.

What you will be doing:

Active participation in the Site Validation Program and general Quality Assurance activities.
Coordination / direction and active participation in the validation and qualification of ABB equipment, utilities, processes and software in compliance with AbbVie policies, FDA, European cGMP and GAMP
standards.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards. QA support for validation investigations and implementation of corrective actions.
Vendor supervision for execution of validation activities.
Execution of Autoclave, Parts washer, Lyo, CIP and SIP ,  VHP and Temperature Mapping  to meet initial validation and revalidation requirements.
Creation/Review/Approval of various validation and qualification documents
Management of validation, exception event, and change control
processes.
Documenting all activities in line with cGMP requirements.
Performing cross training within the team and training of new team
members.
Participation in continuous improvement programs to implement
improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team
members.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Relevant degree and 5 years’ experience
Autoclave validation execution experience
Aseptic processing validation including media fills and VHP validation execution
HVAC validation

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineer Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-28 09:44:38]]></date><referencenumber><![CDATA[1794-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1794&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a contract Validation Engineer for our clients aseptic manufacturing facility in the Connaught region.
 
Why you should apply:

This role will provide you the opportunity to get exposure to a broad range of validation activities on site, and you
You will be responsible for co-ordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements.

What you will be doing:

Active participation in the Site Validation Program and general Quality Assurance activities.
Coordination / direction and active participation in the validation and qualification of ABB equipment, utilities, processes and software in compliance with AbbVie policies, FDA, European cGMP and GAMP
standards.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards. QA support for validation investigations and implementation of corrective actions.
Vendor supervision for execution of validation activities.
Execution of Autoclave, Parts washer, Lyo, CIP and SIP ,  VHP and Temperature Mapping  to meet initial validation and revalidation requirements.
Creation/Review/Approval of various validation and qualification documents
Management of validation, exception event, and change control
processes.
Documenting all activities in line with cGMP requirements.
Performing cross training within the team and training of new team
members.
Participation in continuous improvement programs to implement
improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team
members.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Relevant degree and 5 years’ experience
Autoclave validation execution experience
Aseptic processing validation including media fills and VHP validation execution
HVAC validation

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Validation Engineer Contractor ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-28 09:44:38]]></date><referencenumber><![CDATA[1794-4]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1794&amp;Itemid=986]]></url><city><![CDATA[Leitrim]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a contract Validation Engineer for our clients aseptic manufacturing facility in the Connaught region.
 
Why you should apply:

This role will provide you the opportunity to get exposure to a broad range of validation activities on site, and you
You will be responsible for co-ordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements.

What you will be doing:

Active participation in the Site Validation Program and general Quality Assurance activities.
Coordination / direction and active participation in the validation and qualification of ABB equipment, utilities, processes and software in compliance with AbbVie policies, FDA, European cGMP and GAMP
standards.
Generation/maintenance/execution of Project Validation Plans and schedules.
Generation of validation protocols and final reports to cGMP standards. QA support for validation investigations and implementation of corrective actions.
Vendor supervision for execution of validation activities.
Execution of Autoclave, Parts washer, Lyo, CIP and SIP ,  VHP and Temperature Mapping  to meet initial validation and revalidation requirements.
Creation/Review/Approval of various validation and qualification documents
Management of validation, exception event, and change control
processes.
Documenting all activities in line with cGMP requirements.
Performing cross training within the team and training of new team
members.
Participation in continuous improvement programs to implement
improvements in manufacturing, quality, safety and training systems.
Coordinating activities to maximize the effectiveness of all of the team
members.
Communicating with peers and management regarding activities in the area, including elevation of events or concerns.

 
What you need to apply:

Relevant degree and 5 years’ experience
Autoclave validation execution experience
Aseptic processing validation including media fills and VHP validation execution
HVAC validation

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Risk Management Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-05-28 10:52:50]]></date><referencenumber><![CDATA[1795]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1795&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Risk Management Manager
Team Horizon is seeking a Risk Management Manager for a client in Dublin. This person will be involved in risk assessments (including physical site/ building/ construction risk)
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:
Business Resilience Program Execution

Support the ongoing operation of the site Business Resilience program across Risk Management, Crisis management, and Business Continuity.
Maintain governance structures, trackers, and reporting to ensure clear visibility of program health.
Ensure alignment with standards while adapting to local site needs

Risk Management

Maintain and actively manage the site risk portfolio, ensuring risks are clearly defined, assessed, and prioritised.
Facilitate risk assessments and ensure actions are progressing and risks are actively managed.
Support preparation of risk reviews and materials for site leadership.

Crisis Management &amp;amp; Incident Readiness

Support coordination of crisis management readiness, including crisis management plans, training, and documentation.
Monitoring of current national and global events which may be impactful to operations or personnel.
Support crisis activations as required, ensuring structured coordination and communication.
Facilitate exercises and incorporate lessons learned into program improvements.

Business Continuity Planning

Support the development and maintenance of Business Continuity plans across site functions in line with network expectations.
Ensure plans remain aligned with current risks, site changes, and operational priorities.
Facilitate Business Continuity exercises and scenario planning activities5. Stakeholder Coordination &amp;amp; Program Integration
Work closely with cross-functional teams including Operations, Engineering, EHS, Quality, Digital, Capital Projects and external partners.
Act as a central point of coordination for risk related activities across the site

 Governance, Reporting &amp;amp; Continuous Improvement

Maintain structured documentation, trackers, and reporting tools to support program oversight.
Prepare clear and concise updates for leadership as required.
Identify opportunities to improve processes, tools, and ways of working within the resilience program.

What you need to apply:
Essential Requirements
Candidates should possess one of the following:

3+ years’ experience in Project Management OR
2+ years’ experience in Risk Management and Business Continuity OR
2+ years’ experience in Environmental Health &amp;amp; Safety (EH&amp;amp;S)

And

2+ years’ relevant experience within Inspection, Packaging and/or Solid Dosage operations in a manufacturing environment.
Experience working within regulated and/or complex operational environments, ideally within pharmaceutical, biotech, or manufacturing industries.
Proven experience facilitating risk assessments and supporting business continuity planning activities.
Strong programme coordination and project management capabilities, with the ability to drive actions through to completion.
Excellent organisational, communication, and stakeholder management skills.
Ability to work independently while effectively managing multiple priorities.
Strong collaborative approach, with experience working cross-functionally alongside technical teams and key stakeholders.
High attention to detail, with a structured and methodical approach to work.
Strong technical writing and documentation skills.

Desirable Requirements

Experience supporting capital projects or large-scale site expansion initiatives.
Familiarity with risk assessment tools and methodologies, including FMEA.
Relevant professional certifications in areas such as FMEA, Business Continuity, Risk Management, or Crisis Management.
Experience applying continuous improvement methodologies.
Proficiency with reporting and project tracking tools such as Power BI, Smartsheet, or similar platforms.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing, EHS]]></category></job><job><title><![CDATA[Project Engineer - System Owner for Syringe Filling ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-04 10:33:19]]></date><referencenumber><![CDATA[1797]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1797&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking an experienced Project Engineer (System Owner) to lead the implementation and operational readiness of syringe filling equipment and associated single-use systems as part of a major site expansion in Dublin.  This is a critical role supporting a high-speed, GMP-regulated fill-finish manufacturing environment.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Act as System Owner (SO) for syringe filling equipment from design through to PQ and commercial operation.
SO during equipment implementation, FAT/SAT, commissioning, qualification (IQ/OQ/PQ), and validation activities
 Drive manufacturing readiness, start-up, and handover to operations.
Ensure compliance with GMP, regulatory, and global standards.
Develop and implement: o Maintenance strategies o Critical spare parts strategy o Preventive maintenance programs o Lifecycle asset management plans
Provide technical leadership during deviation investigations, troubleshooting, and performance optimisation.
Partner cross-functionally with Manufacturing, Quality, Automation, Validation, EHSS, and Global Engineering.
Support new product introduction and technology transfer activities.

What you need to apply:

Bachelor’s Degree in Mechanical, Electrical, Chemical, or related Engineering discipline.
5+ years’ experience in biopharmaceutical manufacturing engineering.
Proven experience in aseptic syringe filling systems (high-speed lines preferred).
Strong knowledge of: o GMP and regulatory expectations o Annex 1 o Aseptic processing principles o Equipment validation lifecycle
Experience with single-use technologies in fill-finish environments desirable.
Demonstrated ability to lead complex equipment projects from design through operational readiness.
Strong troubleshooting and root cause analysis capability

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-04 11:55:45]]></date><referencenumber><![CDATA[1798]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1798&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Senior Project Engineer
 
Team Horizon is seeking a Senior Project Engineer for a leading pharmaceutical company in Athlone.
The Project Engineer will lead the equipment purchase, delivery installation and qualification of the processing equipment on site. Overseeing, leading and supporting the work of the other project engineers. 
New Processing equipment with some Facility / utilities modifications to incorporate same.
 
Why you should apply:

•          Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.


•          You enjoy working on exciting projects and want to work with a global manufacturing site in Athlone

 
What you will be doing:
•          Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. 
•          Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel.
•          Writing User Requirement Specifications.
•          Selecting Vendors and completing Vendor evaluation matrix.
•          Managing contractors and project schedules.
•          Writing RCE's, placing orders, Project Management &amp;amp; Design review meetings.
•          Lead the Project Team participation in Factory Acceptance Testing program.
•          Coordination of all equipment documentation requirements.
•          Commissioning of equipment and Engineering support during qualification.
•          Work with the E&amp;amp;T Senior Manager &amp;amp; System Owner / Project Team.
•          Handover training, coordination of O&amp;amp;M manuals, Spare parts, &amp;amp; PM schedules.
•          Lead your regular weekly / bi-weekly Project review meetings with your Project team.
 
What you need to apply:
•          Third level qualification in an Engineering or equivalent discipline/experience.
•          Experience of working in Biologics, Pharmaceuticals or Medical device industry.
•          Min of 3 to 5 years’ experience in sterile filling/manufacturing process.
•          Project management experience with proven record.
•          Assured self-starter with proven technical ability.
•          Good communication and interpersonal skills required to operate in a multi-function project team set up.
•          Ability to work within a team using your own initiative to articulate and deliver specific functional requirements for all aspects of the project and work with members of various disciplines and functions across the project.
•          Good team leading skills and ability to work closely with other areas/departments within an organization.]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-04 11:55:45]]></date><referencenumber><![CDATA[1798-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1798&amp;Itemid=986]]></url><city><![CDATA[Westmeath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Senior Project Engineer
 
Team Horizon is seeking a Senior Project Engineer for a leading pharmaceutical company in Athlone.
The Project Engineer will lead the equipment purchase, delivery installation and qualification of the processing equipment on site. Overseeing, leading and supporting the work of the other project engineers. 
New Processing equipment with some Facility / utilities modifications to incorporate same.
 
Why you should apply:

•          Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.


•          You enjoy working on exciting projects and want to work with a global manufacturing site in Athlone

 
What you will be doing:
•          Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. 
•          Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel.
•          Writing User Requirement Specifications.
•          Selecting Vendors and completing Vendor evaluation matrix.
•          Managing contractors and project schedules.
•          Writing RCE's, placing orders, Project Management &amp;amp; Design review meetings.
•          Lead the Project Team participation in Factory Acceptance Testing program.
•          Coordination of all equipment documentation requirements.
•          Commissioning of equipment and Engineering support during qualification.
•          Work with the E&amp;amp;T Senior Manager &amp;amp; System Owner / Project Team.
•          Handover training, coordination of O&amp;amp;M manuals, Spare parts, &amp;amp; PM schedules.
•          Lead your regular weekly / bi-weekly Project review meetings with your Project team.
 
What you need to apply:
•          Third level qualification in an Engineering or equivalent discipline/experience.
•          Experience of working in Biologics, Pharmaceuticals or Medical device industry.
•          Min of 3 to 5 years’ experience in sterile filling/manufacturing process.
•          Project management experience with proven record.
•          Assured self-starter with proven technical ability.
•          Good communication and interpersonal skills required to operate in a multi-function project team set up.
•          Ability to work within a team using your own initiative to articulate and deliver specific functional requirements for all aspects of the project and work with members of various disciplines and functions across the project.
•          Good team leading skills and ability to work closely with other areas/departments within an organization.]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Quality Systems Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-09 12:39:23]]></date><referencenumber><![CDATA[1799]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1799&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[An exciting opportunity available for a Quality Systems Specialist. This is a hybrid role and is an initial 12-month contract.
 
Why you should apply:

Join a progressive company with state-of-the-art working facilities, which include an onsite gym and flexible working conditions such as flex hours and work from home
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.

 
What you will be doing:

Responsibility and oversight for the development and maintenance of site quality systems, quality compliance and related procedures and processes, including but not limited to, Documentation Management, Change Control, Deviation/CAPA processes, oversight of applicable QMS systems supporting and the overall Quality Management Review process.
Provide Quality direction and input at Change Control and Deviation Review Boards and assume oversight of change control and Deviation/CAPA records; ensuring scope of record is clear and implementation activities are robust and timely.
Oversee and implement Quality Agreements relating to area of responsibility.
Keep abreast of regulatory initiatives and new guidance/requirements and for the communication of revised guidelines associated to Quality Systems.
Responsible for sustained compliance initiatives, including execution of gap assessments in support of revised operating Standards and/or Corporate policies &amp;amp; procedures.
Oversight and management of Quality Risk Management (QRM) Processes and for the embedding of QRM principles within the quality framework.
Ownership, accountability and provision of Subject Matter Expertise for key quality Systems, including Change Control, Deviation/CAPA processes and Documentation Management.
Responsible for trending programs associated with Deviation/CAPA, Change Control, Complaints, Periodic Reviews, QRM, ensuring that trend programs and outputs are providing key indicators as to program efficacy.
Responsible for challenging current procedures and practices, interpretation of trend data and for making any necessary revisions to quality programs to afford optimisation and further development of existing quality standards and overall compliance.
In line with business requirements, these responsibilities may expand or otherwise include additional areas of responsibility which are not described in this specification but are associated with the role. The knowledge and skills necessary to perform the duties of the QA Specialist are typically acquired through the following combination of education, experience and knowledge.
Ensuring that self-inspection, audit and key compliance systems are effectively implemented, revised and optimized to ensure a continuous drive to improve product and process quality at site.

 
What you need to apply:

University degree. Engineering or Science related discipline preferred.
Relevant experience (3yrs +) working in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the requirements of the role.
Excellent written and verbal communication skills
Experience working with dynamic cross-functional teams and proven abilities in decision making
Strong organizational skills, including ability to follow assignments through to completion
Demonstrated ability in problem solving and experience in managing Root Cause Analysis / Deviation investigations.
Detailed Knowledge of applicable Regulatory requirements. Experience with Regulatory inspections.
Experience working in aseptic operations, protein formulation, vial and syringe filling

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Supply Planning Transformation Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-10 17:19:44]]></date><referencenumber><![CDATA[1800]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1800&amp;Itemid=986]]></url><city><![CDATA[Remote]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Supply Chain Planning professional to Serve as the dedicated site transformation resource responsible for deploying the program at assigned manufacturing sites.
You will Guide the site team through the full transition to the new Target Operating Model (TOM), ensuring sustainable adoption of new processes, tools, and ways of working and bridge the gap between the central deployment program and the site, translating strategic transformation objectives into practical, site-level outcomes
 
 
Why you should apply:

Join a company who strive to have a remarkable impact on people's lives across several key therapeutic areas – and are committed to operating with integrity.

 
 
What you will be doing:

Manage Own the end-to-end deployment of the Future Focused Planning program at assigned manufacturing sites.
Partner with site leadership and supply planning teams to drive adoption of the new Target Operating Model (TOM).
Conduct site readiness assessments and identify gaps against the target state.
Develop and execute site-specific deployment and change management plans.
Deliver training and capability-building sessions for site supply planning teams.
Track and report site progress against deployment milestones and KPIs to the Deployment Lead.
Identify and escalate risks and issues in a timely manner.
Embed new ways of working, processes, and tools at site level to ensure lasting change.
Capture and share site learnings to support continuous improvement of the overall deployment approach.
Ensure the site is fully prepared for post-deployment sustainability and hypercare exit.

 
 
What you need to apply:

Bachelor's degree in Supply Chain Management, Business Administration, Industrial Engineering, or related field (required). Master's degree or professional specialization in Supply Chain/Operations (preferred).
5–8 years of experience in supply planning, demand planning, or S&amp;amp;OP in a manufacturing environment.
Understanding of operating model design and transformation program delivery.
Strong facilitation, training, and stakeholder engagement skills.
Analytical mindset with the ability to identify gaps and drive pragmatic solutions.
Comfortable working independently at site level with minimal supervision.
Practical knowledge of SAP, IBP, or equivalent planning tools (desirable).
Change management knowledge or certification (desirable).
 
]]></description><jobtype><![CDATA[Remote, Contractor]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[Capital works Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-15 15:58:38]]></date><referencenumber><![CDATA[1801]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1801&amp;Itemid=986]]></url><city><![CDATA[Wexford]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Capital Works Project Manager for a company based in Kilkenny and the South East.
Managing the preparation of a comprehensive brief for the projects in consultation with services and capital &amp;amp; estates personnel and advisors.
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

You enjoy working in a culture of learning and collaboration and making a positive impact.
Provide services as appropriate in the development and execution of major capital projects in ACUTE and NON-ACUTE settings and to plan and supervise the execution of these projects by:
Ensuring that the brief is known and understood, in appropriate detail, by all those who are likely to work in the new facility.
Managing the necessary and appropriate consultation processes, meetings and other activities necessary to satisfactory completion of the project.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Acting as senior administrative officer for the management of the project and helping to resolve quickly such issues as may be for resolution and agreement.
Defining requirements for design services, buildings and equipment.
Advising on the selection of Design Teams, other professional services and Contractors for Capital Projects, arranging and managing the procurement processes.
Arranging for preparation of specifications, drawing and contract documents for Capital Projects.
Obtaining approval to proposals as necessary in accordance with protocols and regulations in a timely manner.
Developing proposals with selected design teams and contractors.
Developing action plans for the timely and efficient completion of contracts.  Co-ordinating the tender and control stages of the project, having close liaison with the design team, site supervisory staff, etc. on the one hand and hospital personnel on the other.
Supervising staff and contractors in the implementation of agreed programmes.
Working with service management and nurse planners  to ensure that the equipping/commissioning team  is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Ensuring that the equipping/commissioning team is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Managing and controlling agreed project timescales and budgets for planning, design, construction and equipping and budgets to agreed quality standards.
Anticipating difficulties and problems, especially those arising from phasing, variations, commissioning and vacating, and ensuring that where necessary these are either resolved directly or brought to the notice of the Estates Manager and Project Board, for decisions on avoidable claims for delays, extras etc.
Managing and controlling expenditure on each assigned project.  This is to include presentations to senior management and Project Board as required, of information and current estimates of total costs, running statements of financial commitment and forecasts of expenditure.
Checking design team fees accounts with regards to agreed fees and preparing same for certification by the Estates Manager.  He/she shall process payments to contractors and design team firms for payment in accordance with constraints set down in contract documents, forms of agreement and statutory provisions.
Advising line management on measures appropriate to enable the orderly phasing out of services in old facilities and the transfer to new facilities of staff and services.
Assisting in the orderly phasing of developments by agreeing appropriate arrangements with line management and to keep line management and senior clinical staff informed of the plans as the developments proceed.
Ensuring appropriate maintenance arrangements are put in place for new buildings.
Plan and supervise the execution of minor capital works by:
Developing a comprehensive brief for the project for minor capital works in consultation with local managers and Maintenance Officers/Engineering Officers.
Preparing or arranging for preparation of plans and contract documents to detail required.
Arranging for the appointment and management of design teams where required.
Arranging for submission of tenders and recommending tenders for acceptance.
Agreeing programme for project with contractors.
Arranging for the management of the minor capital works.
Ensuring that agreed programme is completed within time and tender sum.
Prepare in consultation with appropriate officers and advisors, programmes for the maintenance of buildings, services, equipment and vehicles (under his/her control).
Defining in accordance with overall guidelines, maintenance requirements of all buildings, services, equipment and vehicles under his/her control, minor capital works and fire precautions schemes and proposing priorities in the allocation of resources available for these schemes.
Preparing budgets for the carrying out of the proposed programmes.
Defining the staff or contract resources necessary to discharge agreed programmes and preparing action plans for carrying out of same.
Draw up, or in appropriate circumstances, arrange for the development of plans and contract arrangements for the implementation of approved capital / maintenance programmes by:
Assisting in defining requirements for all equipment and buildings, especially in seeking ease of maintenance and operation.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Recommending awards of maintenance contracts to outside contractors where for economical or practical considerations such is considered desirable.
Developing proposals with selected contractors.
Obtaining departmental approval to proposals as necessary.
Developing action plans for the timely and efficient completion of all contracts.
Supervising staff and contractors in the implementation of the agreed programme.
Managing and controlling the agreed budget.
Ensure that all buildings, services, equipment and vehicles under his/her control are adequately maintained in accordance with the approved maintenance programmes by:
Developing planned maintenance routines for all relevant equipment based on manufacturer’s instructions, equipment importance and usage rates.
Incorporating maintenance requirements in supply contracts for new equipment and vehicles where appropriate.
Developing regular inspection and maintenance routines for all buildings, services, equipment and vehicles.
Developing guidelines for the safe operation of all equipment.
Work with and support the activities of the Property Manager to ensure compliance with Property Transaction Protocols and other relevant property related tasks when assigned such as:
Property management and technical advisory services as deemed appropriate for the management of the healthcare estate property portfolio within the assigned area.
To work with the Property Manager to develop and implement a property management strategy and local property plans in collaboration with other key personnel and advisors.
To work with the Property Manager to ensure property requirements are fully integrated with service provision and staffing levels and ensure all cross care group opportunities for property utilisation are maximised within the Property portfolio.
To work with the Property Manager to ensure that all property transactions conform to statutory requirements.
To assess the physical infrastructure of the property portfolio including purpose, state of upkeep, capacity, suitability, space utilisation and security.
Provide information to the Property Manager so as to maintain and keep a property asset register including appropriate records of the legal title to properties.
Ensure that adequate fire prevention and safety measures and standards are devised and applied by:
Discussing with the local authority Fire Officer in the area in association with the Service Manager and Fire Prevention Officers and other relevant staff, fire precaution and safety measures, and their priorities.
Providing a programme for implementation of agreed measures and arranging for employment and training of sufficient fire prevention officers.
Advising and agreeing annual programmes for fire precautions schemes after consultation with local authority Fire Officers in the area and the Service Managers and Fire Prevention Officers.
Provide advice on the efficient use of energy and work with services personnel and other capital &amp;amp; estates personnel and advisors on the efficient use of energy in healthcare premises by;
Monitoring and reporting on the energy consumption in healthcare premises.
Assessing the energy efficiency standards in premises in accordance with current standards and regulations.
Advising on investment proposals in energy saving projects.
Preparing and implementing agreed investment proposals on energy saving projects.
Advise on facilities and environmental matters in conjunction with services personnel and other capital &amp;amp; estates personnel, and advisors as required by:
Assisting as necessary in assessing Health &amp;amp; Safety of facilities and environmental risks.
Co-operating with Fire and Safety Officers, Services Managers, Health &amp;amp; Safety, Risk Management, Occupational Health and Infection Control Staff in addressing facilities improvements with regard to legislative compliance.
Adequately identifies, assesses, manages and monitors risk within their area of responsibility.
Engage in the performance achievement process in conjunction with your Line Manager and staff as appropriate.
Co-operate with the Health Services Transformation Programme as required to carry out the duties of the post.
Have a working knowledge of the Health Information and Quality Authority (HIQA) Standards as they apply to the role for example, Standards for Healthcare, National Standards for the Prevention and Control of Healthcare Associated Infections, Hygiene.
All other duties as requested or assigned.

 
What you need to apply:

Hold a Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) major academic award in Architecture, Engineering or Surveying accredited by the relevant Professional Institute (Society of Chartered Surveyors in Ireland, Royal Institution of Chartered Surveyors, Engineers Ireland, Royal Institute of Architects of Ireland).
Have Full Membership of the relevant professional association: - Society of Chartered Surveyors in Ireland - Royal Institution of Chartered Surveyors - Engineers Ireland - Royal Institute of Architects of Ireland
Have had at least seven years’ satisfactory &amp;amp; relevant experience in planning, design, project management or construction of buildings or in the installation or maintenance of the mechanical, electrical, and heating services of such buildings.
Candidates must possess the requisite knowledge and ability (including a high standard of suitability and of administrative capacity) for the proper discharge of the duties of the office.
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Capital works Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-15 15:58:38]]></date><referencenumber><![CDATA[1801-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1801&amp;Itemid=986]]></url><city><![CDATA[Wicklow]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Capital Works Project Manager for a company based in Kilkenny and the South East.
Managing the preparation of a comprehensive brief for the projects in consultation with services and capital &amp;amp; estates personnel and advisors.
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

You enjoy working in a culture of learning and collaboration and making a positive impact.
Provide services as appropriate in the development and execution of major capital projects in ACUTE and NON-ACUTE settings and to plan and supervise the execution of these projects by:
Ensuring that the brief is known and understood, in appropriate detail, by all those who are likely to work in the new facility.
Managing the necessary and appropriate consultation processes, meetings and other activities necessary to satisfactory completion of the project.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Acting as senior administrative officer for the management of the project and helping to resolve quickly such issues as may be for resolution and agreement.
Defining requirements for design services, buildings and equipment.
Advising on the selection of Design Teams, other professional services and Contractors for Capital Projects, arranging and managing the procurement processes.
Arranging for preparation of specifications, drawing and contract documents for Capital Projects.
Obtaining approval to proposals as necessary in accordance with protocols and regulations in a timely manner.
Developing proposals with selected design teams and contractors.
Developing action plans for the timely and efficient completion of contracts.  Co-ordinating the tender and control stages of the project, having close liaison with the design team, site supervisory staff, etc. on the one hand and hospital personnel on the other.
Supervising staff and contractors in the implementation of agreed programmes.
Working with service management and nurse planners  to ensure that the equipping/commissioning team  is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Ensuring that the equipping/commissioning team is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Managing and controlling agreed project timescales and budgets for planning, design, construction and equipping and budgets to agreed quality standards.
Anticipating difficulties and problems, especially those arising from phasing, variations, commissioning and vacating, and ensuring that where necessary these are either resolved directly or brought to the notice of the Estates Manager and Project Board, for decisions on avoidable claims for delays, extras etc.
Managing and controlling expenditure on each assigned project.  This is to include presentations to senior management and Project Board as required, of information and current estimates of total costs, running statements of financial commitment and forecasts of expenditure.
Checking design team fees accounts with regards to agreed fees and preparing same for certification by the Estates Manager.  He/she shall process payments to contractors and design team firms for payment in accordance with constraints set down in contract documents, forms of agreement and statutory provisions.
Advising line management on measures appropriate to enable the orderly phasing out of services in old facilities and the transfer to new facilities of staff and services.
Assisting in the orderly phasing of developments by agreeing appropriate arrangements with line management and to keep line management and senior clinical staff informed of the plans as the developments proceed.
Ensuring appropriate maintenance arrangements are put in place for new buildings.
Plan and supervise the execution of minor capital works by:
Developing a comprehensive brief for the project for minor capital works in consultation with local managers and Maintenance Officers/Engineering Officers.
Preparing or arranging for preparation of plans and contract documents to detail required.
Arranging for the appointment and management of design teams where required.
Arranging for submission of tenders and recommending tenders for acceptance.
Agreeing programme for project with contractors.
Arranging for the management of the minor capital works.
Ensuring that agreed programme is completed within time and tender sum.
Prepare in consultation with appropriate officers and advisors, programmes for the maintenance of buildings, services, equipment and vehicles (under his/her control).
Defining in accordance with overall guidelines, maintenance requirements of all buildings, services, equipment and vehicles under his/her control, minor capital works and fire precautions schemes and proposing priorities in the allocation of resources available for these schemes.
Preparing budgets for the carrying out of the proposed programmes.
Defining the staff or contract resources necessary to discharge agreed programmes and preparing action plans for carrying out of same.
Draw up, or in appropriate circumstances, arrange for the development of plans and contract arrangements for the implementation of approved capital / maintenance programmes by:
Assisting in defining requirements for all equipment and buildings, especially in seeking ease of maintenance and operation.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Recommending awards of maintenance contracts to outside contractors where for economical or practical considerations such is considered desirable.
Developing proposals with selected contractors.
Obtaining departmental approval to proposals as necessary.
Developing action plans for the timely and efficient completion of all contracts.
Supervising staff and contractors in the implementation of the agreed programme.
Managing and controlling the agreed budget.
Ensure that all buildings, services, equipment and vehicles under his/her control are adequately maintained in accordance with the approved maintenance programmes by:
Developing planned maintenance routines for all relevant equipment based on manufacturer’s instructions, equipment importance and usage rates.
Incorporating maintenance requirements in supply contracts for new equipment and vehicles where appropriate.
Developing regular inspection and maintenance routines for all buildings, services, equipment and vehicles.
Developing guidelines for the safe operation of all equipment.
Work with and support the activities of the Property Manager to ensure compliance with Property Transaction Protocols and other relevant property related tasks when assigned such as:
Property management and technical advisory services as deemed appropriate for the management of the healthcare estate property portfolio within the assigned area.
To work with the Property Manager to develop and implement a property management strategy and local property plans in collaboration with other key personnel and advisors.
To work with the Property Manager to ensure property requirements are fully integrated with service provision and staffing levels and ensure all cross care group opportunities for property utilisation are maximised within the Property portfolio.
To work with the Property Manager to ensure that all property transactions conform to statutory requirements.
To assess the physical infrastructure of the property portfolio including purpose, state of upkeep, capacity, suitability, space utilisation and security.
Provide information to the Property Manager so as to maintain and keep a property asset register including appropriate records of the legal title to properties.
Ensure that adequate fire prevention and safety measures and standards are devised and applied by:
Discussing with the local authority Fire Officer in the area in association with the Service Manager and Fire Prevention Officers and other relevant staff, fire precaution and safety measures, and their priorities.
Providing a programme for implementation of agreed measures and arranging for employment and training of sufficient fire prevention officers.
Advising and agreeing annual programmes for fire precautions schemes after consultation with local authority Fire Officers in the area and the Service Managers and Fire Prevention Officers.
Provide advice on the efficient use of energy and work with services personnel and other capital &amp;amp; estates personnel and advisors on the efficient use of energy in healthcare premises by;
Monitoring and reporting on the energy consumption in healthcare premises.
Assessing the energy efficiency standards in premises in accordance with current standards and regulations.
Advising on investment proposals in energy saving projects.
Preparing and implementing agreed investment proposals on energy saving projects.
Advise on facilities and environmental matters in conjunction with services personnel and other capital &amp;amp; estates personnel, and advisors as required by:
Assisting as necessary in assessing Health &amp;amp; Safety of facilities and environmental risks.
Co-operating with Fire and Safety Officers, Services Managers, Health &amp;amp; Safety, Risk Management, Occupational Health and Infection Control Staff in addressing facilities improvements with regard to legislative compliance.
Adequately identifies, assesses, manages and monitors risk within their area of responsibility.
Engage in the performance achievement process in conjunction with your Line Manager and staff as appropriate.
Co-operate with the Health Services Transformation Programme as required to carry out the duties of the post.
Have a working knowledge of the Health Information and Quality Authority (HIQA) Standards as they apply to the role for example, Standards for Healthcare, National Standards for the Prevention and Control of Healthcare Associated Infections, Hygiene.
All other duties as requested or assigned.

 
What you need to apply:

Hold a Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) major academic award in Architecture, Engineering or Surveying accredited by the relevant Professional Institute (Society of Chartered Surveyors in Ireland, Royal Institution of Chartered Surveyors, Engineers Ireland, Royal Institute of Architects of Ireland).
Have Full Membership of the relevant professional association: - Society of Chartered Surveyors in Ireland - Royal Institution of Chartered Surveyors - Engineers Ireland - Royal Institute of Architects of Ireland
Have had at least seven years’ satisfactory &amp;amp; relevant experience in planning, design, project management or construction of buildings or in the installation or maintenance of the mechanical, electrical, and heating services of such buildings.
Candidates must possess the requisite knowledge and ability (including a high standard of suitability and of administrative capacity) for the proper discharge of the duties of the office.
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Quality Assurance Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-16 17:11:47]]></date><referencenumber><![CDATA[1802]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1802&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Quality Assurance Specialist on a hybrid basis on an initial 12-month contract.
This Quality Assurance oversight and subject matter expertise for deviations, investigations, CAPAs, and change controls. Working closely with Manufacturing, Engineering, Validation, Quality Control, and Supply Chain, the role ensures quality investigations are managed effectively and in compliance with GMP requirements, regulatory expectations.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Provide QA oversight of deviations, investigations, CAPAs, and change controls, ensuring timely and compliant execution.
Review and approve quality records, ensuring appropriate scope, root cause analysis, risk assessment, and corrective actions.
Represent QA at Deviation Review Boards, Change Control Boards, and other cross-functional forums.
Support complex investigations and provide quality guidance on compliance and operational issues.
Monitor quality system trends and support continuous improvement initiatives.
Contribute to Annual Product Reviews and quality metrics reporting, as required.
Support internal audits, regulatory inspections, and inspection readiness activities.
Perform all activities in compliance with safety standards and SOPs.
Responsibilities may expand to include additional areas aligned with business needs.

 
What you need to apply:

Bachelor’s degree in science, Engineering, Pharmacy, Biotechnology, or a related discipline. - Minimum 5 years' experience in the pharmaceutical or biotechnology industry
Experience providing QA oversight of deviations, investigations, CAPAs, and change controls in a GMP environment.
Strong understanding of GMP requirements, quality systems, and risk management principles.
Strong analytical, problem-solving, communication, and stakeholder management skills.
Ability to work independently and effectively in a cross-functional environment.
Excellent organisational, communication, coordination, and meeting facilitation skills.
Proven track record of supporting continuous improvement initiatives within a regulated environment

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Equipment Maintenance Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-17 12:27:25]]></date><referencenumber><![CDATA[1803]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1803&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Equipment Maintenance Technician for a leading pharmaceutical company in North Dublin.
The Maintenance Technician performs functions related to supporting the manufacture of drug products, such as setting-up, cleaning, and maintaining equipment and facilities.
The role assists in troubleshooting equipment issues and observes established escalation paths to ensure issues are appropriately addressed and resolved so production targets can be met.
The Maintenance Technician is responsible for the safe, compliant, and efficient execution of job duties in a team environment. This position reports to the Maintenance Supervisor.
2 cycle shift @ 20%; rotating weeks of days (06:30 – 14:30) and evenings (14:20 – 23:00) (Fridays: 14:20 – 19:30).
1 week of nights every 6 weeks @ 33%; 22:30 – 07:30 (Fridays: 19:30 - 03:30) which would coincide with a week that they are supposed to be on evenings.
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Dublin.

 
What you will be doing:

Support and adhere to established maintenance schedules.
Maintain production and facility equipment in strict accordance with maintenance instructions, SOPs, and cGMPs.
Complete all required data entries with detail and accuracy in real time.
Observe established escalation process for issues impacting established production-related Service Level Agreements (SLAs) and/or fulfillment of production goals.
Recognize and report to immediate supervisor any process or equipment anomalies and/or deviations from accepted standards.
Provide status updates on maintenance activities and operational challenges according to defined procedures.
Execute machine changeovers between batches according to established SOPs and SLAs.
Keep work area neat and orderly and observe all safety and compliance procedures.
Seek process innovation and continuous process improvement in production area.
Complete and conform to all training requirements for job role, including company-required and role-specific training.
Carry out and assist in the ongoing training of new and existing personnel, as appropriate.
Observe all safety and compliance procedures and actively highlight any safety concerns to help drive the reduction of accidents or near misses.
May participate in department initiatives and projects.
Any other duties as assigned.

 
What you need to apply:

Minimum of mechanical, electrical, or instrumentation craft qualification – preferably in the Pharmaceutical industry.
Preferably 5 years GMP/pharmaceutical maintenance work experience.
Basic Microsoft Excel and Word skills.
Maximo and Track Wise knowledge desirable.
Equipment: related to Oral Solid Dose (capsules/tablets) - blenders, granulators, tablet capsulation equipment, presses.
Minimum of mechanical or electrical craft qualification
Strong Mechanical and electrical faultfinding skills. 90% of work will be mechanical but they would need a good understanding of electrical for the night shift.
At least 3 years experience in Pharma manufacturing environment (Oral Solid Dose) or similar (med device/food)
Ability to read and understand mechanical drawings, technical manuals, electrical wiring schematics, layout drawings and P&amp;amp;ID’s.

Previous experience using a Computerised Maintenance Management System (CMMS)]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[QA Specialist Deviations ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-17 16:05:32]]></date><referencenumber><![CDATA[1804]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1804&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Quality Assurance Specialist on a hybrid basis on an initial 12-month contract.
This Quality Assurance oversight and subject matter expertise for deviations, investigations, CAPAs, and change controls. Working closely with Manufacturing, Engineering, Validation, Quality Control, and Supply Chain, the role ensures quality investigations are managed effectively and in compliance with GMP requirements, regulatory expectations.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Provide QA oversight of deviations, investigations, CAPAs, and change controls, ensuring timely and compliant execution.
Review and approve quality records, ensuring appropriate scope, root cause analysis, risk assessment, and corrective actions.
Represent QA at Deviation Review Boards, Change Control Boards, and other cross-functional forums.
Support complex investigations and provide quality guidance on compliance and operational issues.
Monitor quality system trends and support continuous improvement initiatives.
Contribute to Annual Product Reviews and quality metrics reporting, as required.
Support internal audits, regulatory inspections, and inspection readiness activities.
Perform all activities in compliance with safety standards and SOPs.
Responsibilities may expand to include additional areas aligned with business needs.

 
What you need to apply:

Bachelor’s degree in science, Engineering, Pharmacy, Biotechnology, or a related discipline. - Minimum 5 years' experience in the pharmaceutical or biotechnology industry
Experience providing QA oversight of deviations, investigations, CAPAs, and change controls in a GMP environment.
Strong understanding of GMP requirements, quality systems, and risk management principles.
Strong analytical, problem-solving, communication, and stakeholder management skills.
Ability to work independently and effectively in a cross-functional environment.
Excellent organisational, communication, coordination, and meeting facilitation skills.
Proven track record of supporting continuous improvement initiatives within a regulated environment

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Senior Payroll Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-18 09:38:00]]></date><referencenumber><![CDATA[1805]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1805&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Payroll Senior Specialist
Team Horizon is seeking a Payroll Senior Specialist for a client in Dublin who will be responsible for delivering payroll using computerised HCM and Payroll systems running typically more than one payroll. Will ensure that the standards of accuracy and the timing requirements of the payroll(s) are met.
 
Why you should apply:

•          This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.


•          Excellent contracting rates on offer.

 
 
What you will be doing:
•          Identifying and delivering process improvement, including where appropriate, automation using currently available automation tools
•          Ensuring adherence to statutory reporting requirements
•          Liaising with senior managers in relation to the impact on the payroll function of HR policies and procedures
•          Coordinating, together with other team members, workloads to cope with peak processing requirements
•          Ensuring compliance with Processes and Legislation and works to minimise financial loss for the business through effective and timely processing
•          Maintaining Payroll Accuracy through execution of effective payroll controls and in line with agreed Key performance Indicators
•          Providing Support and Input on Payroll Related Projects
•          Assisting with audits and finance queries
•          Maintaining, updating and helping create relevant Payroll policies, procedures, forms and knowledge articles as and when required
•          Minimising loss from the business by enacting timely processing of leavers and payments
 
What you need to apply:
•          5+ years’ payroll experience in a hands-on role
•          Strong knowledge of payroll, taxation, and insurance schemes
•          Experience in large organisations
•          Proficiency with payroll systems (e.g. ADP, Workday)
•          Strong analytical, problem-solving, and communication skills
•          High attention to detail with the ability to meet deadlines
•          Process improvement mindset and stakeholder management skills
 
Desirable
•          Degree qualification
•          Multi-country payroll experience
•          Payroll or finance qualification
•          Advanced Excel skills
•          Experience with automation, AI, or machine learning tools]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Accountancy/Finance]]></category></job><job><title><![CDATA[Associate Director Technical Operations]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-18 10:05:18]]></date><referencenumber><![CDATA[1806]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1806&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking an Associate Director Technical Operations for our client based in Mayo. The Associate Director Technical Operations will report to the Director of the Tech Center business unit and be responsible for the Site New Product Introduction Programs. This position has responsibility for providing direct oversight, management, and leadership with minimal technical or administrative guidance, as well as responsibility for all aspects of technical process support such as but not limited to project management, process monitoring and validation programs within the site.
This includes leadership of in-line product support for processes, project definition and demonstration, and process improvements/productivity while assuring compliance with regulatory agencies. These activities involve economic feasibility studies toward objectives assigned or approved by site leadership.
 
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Lead personnel (team of 7-9) responsible for New Product Introduction Programs of the site for Biologics.
Drive Drug Product Technology transfers to manufacturing, including the financial aspects of each project.
Provide technical guidance and continuous improvement support for commercial and new product introductions on day-to-day production and processing issues: problem solving, deviations, manufacturing documentation changes, etc
Source for plant consistency across the Division, share problem-solving activities, and maintain updated technical product history.
Provide technical assistance with the implementation of changes in manufacturing equipment, batch size, ingredient supplier and experimental batches as needed. Ensure that products and processes are kept in compliance with validation requirements.
Identify and solve technical problems independently for new products and for commercial operations.
Plan data collection organizes results and applies statistical methodology. Presents numerical information through computer readouts, graphs, charts and tables, written reports and/or other methods.
Evaluate new process equipment and advises management about areas of opportunity in the application of novel technologies.
Implement at plant level global technical initiatives as: new technologies, suppliers, methods, etc. and provide tactical perspectives.
Assure fulfilments of environmental, health, and safety (EH&amp;amp;S) requirements and compliance obligations, promote continuous improvement, and consider EH&amp;amp;S aspects during the design and change process.

 
What you need to apply:

M.Sc. in a relevant Science area and extensive experience in a “hands on” Process Engineering or development for new product introduction position.
Experience of managing and leading professional teams that include Engineers and or Scientist personnel.
Experience leading product transfer and New Product Introduction projects. Regulatory filing experience as well as familiarity with HA audits.
Excellent communication and interpersonal skills for interaction with both internal departments and other sites worldwide (QA, Validation, IS, EHS, R&amp;amp;D, S&amp;amp;T).
Computer literate with knowledge of statistical methods, data assimilation and interpretation.
Capable to positively influence department employees and/or contributors from other disciplines or peers of higher managerial levels to obtain decision approvals for critical courses of action, either exception or planned.

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering, Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[HR Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-18 10:45:51]]></date><referencenumber><![CDATA[1807]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1807&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a HR Manager for a multinational company in the West of Ireland. As HR Manager, you’ll play a strategic leadership role in shaping workplace culture, driving employee engagement, advancing diversity and inclusion, and building talent pipelines that support business growth.
 
 
Why you should apply:

Be part of a company where innovation, collaboration, and purpose come together to improve millions of lives worldwide.
This is an opportunity to contribute not only to business success, but also to communities and environmental sustainability—making a lasting difference within healthcare and beyond.

 
What you will be doing:

Develop and deliver HR strategies, programs, and services that align with the needs of the respective business.
Partner with the Site Leadership Team to shape a culture of high employee engagement, performance, diversity, and inclusion.
Coach business leaders on HR practices to enhance talent pipeline development, retention, and increase organizational effectiveness.
Utilize data analysis and survey results to generate insights around talent, culture, and engagement.
Collaborate with HR Centers of Excellence to implement HR programs that support the People Strategy and Organizational Goals, including organizational effectiveness and change management.
Provide guidance and counseling to managers and employees on employee relations, discipline, and performance.
Ensure compliance with all legal requirements and work closely with Legal counsel on situations that pose a litigation risk or other liability.
Collaborate with HR Operations and business leaders to ensure appropriate employee documentation, changes to employee status, pay and benefits, annual performance review process, employee relations investigations, discipline, and terminations to maintain compliance with policies and regulations.

 
What you need to apply:

Bachelor’s degree in human resources, Business Studies, or related discipline (CIPD membership preferred).
Extensive HR Business Partner, including expertise in at least one other HR specialism. Successful track record in employee relations, leadership development, and applying HR best practices in a fast-paced environment.
Excellent interpersonal, communication, and analytical skills, with demonstrated ability to influence and advise at all levels.
Solid understanding of Irish employment law and HR compliance requirements.
Passion for people, business acumen, and eagerness to work in a dynamic, growth-oriented organisation.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[HR/Recruitment]]></category></job><job><title><![CDATA[Cleaning Validation Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-23 13:05:35]]></date><referencenumber><![CDATA[1808]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1808&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Cleaning Validation Technical Specialist for our clients Bulk Drug Substance manufacturing facility in Dublin.
 
 
Why you should apply:
• An excellent opportunity to join a growing, progressive and diverse company who unleash bold thinking with the power to inspire life-changing medicines.
 
 
What you will be doing:
• The Cleaning Validation Technical Specialist will support the cleaning validation activities for the cGMP manufacture of biological bulk drug substance 
• The Specialist will provide cleaning validation expertise to support the facility design, start-up and routine commercial manufacturing.
• Responsible for validation and verification of the cleaning used to support the technology transfer of new or existing drug substance manufacturing processes to the facility, and will be required to work in close collaboration with Process Development, Engineering, Supply Chain, Quality, Regulatory and other involved departments to ensure successful facility design, construction, startup and qualification. 
• The position is accountable for timely completion of cleaning validation/verification related milestones, with particular emphasis on cleaning validation for a multi-product drug substance manufacturing facility
• Principal Responsibilities:
• Maintain/update input to the Cleaning/Validation Master Plan to support the multi-product drug substance manufacturing facility 
• Develop and implement/update cleaning strategies for fixed and mobile equipment
• Development/update and/or optimize cleaning (CIP) cycles/methods/recipes for buffer and media preparation systems, upstream (bioreactors) and downstream equipment trains, parts washers and supporting process equipment.
• Generate and execute cleaning validation protocols as required.
• Provide input to Standard Operating Procedures (SOPs) and Work Instructions (WI) to enable suitable cleaning sampling activities to occur.
• Support the cleaning monitoring programme.
 
 
 
What you need to apply:
• 1 - 3 Years of Experience in a similar role 
• Minimum requirement B.Sc. in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Enginee
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality]]></category></job><job><title><![CDATA[Sr Associate Quality Control]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-24 13:57:52]]></date><referencenumber><![CDATA[1809]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1809&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Sr Associate Quality Control for our client based in Dublin. In this role you will be expected, Under minimal supervision, responsible for one or more of the following activities in QC including analytical testing, characterization, sample and data management. You will contribute to team by ensuring the quality of the tasks/services provided by self and contribute to the completion of milestones associated with specific projects or activities within team.
 
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

With a high degree of technical flexibility, work across diverse areas within QC
Plan and perform analyses with great efficiency and accuracy.
Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
Report, evaluate, back-up/archive, trend and approve analytical data.
Troubleshoot, solve problems and communicate with stakeholders.
Initiate and/or implement changes in controlled documents.
May train others as necessary
Participate in audits, initiatives and projects that may be departmental or organizational in scope.
Write protocols and perform assay validation and equipment qualification/ verification.
Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
May contribute to regulatory filings.
 May conduct lab investigations as necessary.
Evaluate lab practices for compliance on a continuous basis.
Approve lab results
May represent the department/organization on various teams
May interact with outside resources.
Create APPX data files and randomisation memo to facilitate data analysis.
LIMS data coordination of commercial and import testing on site where applicable
May provide technical guidance. May contribute to regulatory filings.
May represent the department/organization on various teams. May train others.
May interact with outside resources

 
What you need to apply:

Bachelor’s degree in a science discipline. 2-3 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
Strong background in Chemistry and Analytical testing is required.
Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. 
Understanding and application of principles, concepts, theories, and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning
Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery 
Applies analytical skills to evaluate and interpret complex situations/ problems using multiple sources of information

Qualitative information
Quantitative research
Trend data
Anticipates and prevents potential problems



 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Financial Analyst]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-26 11:59:43]]></date><referencenumber><![CDATA[1811]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1811&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Financial Analyst
Team Horizon is seeking a Financial Analyst in Dublin. The Financial Analyst will support the financial governance, cost control, and reporting functions for the redevelopment programme in the healthcare sector.
Working within the Contracts and Claims team, the role focuses on monitoring project expenditure, analysing financial data, preparing forecasts and budgets, and supporting financial planning across a major capital programme.
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

What you will be doing:

Support the provision of financial oversight and cost monitoring across the project, ensuring accurate tracking of expenditure against approved budgets. This will be achieved through the use of the financial / cost management digital tooling platform established for the programme.
Support with the tracking and reporting of an agreed Cost Breakdown Structure (CBS) aligned with the programme Work Breakdown Structure (WBS).
Assist in the preparation of financial modelling and budget projections for programme and project activities.
Support the Contracts and Claims team in the preparation of financial plans, earned value and cost to complete analysis and forecasting of projected costs to ensure accurate robust and reliable cash flow forecasting for the entire programme.
Analyse financial and cost data to support the development of programme budgets, forecasts and financial performance monitoring.
Assist in the implementation of cost control and financial governance measures to ensure programme delivery within approved budget parameters.
Work collaboratively with Contracts and Claims team and other key stakeholders to establish cost objectives and monitor expenditure throughout the project lifecycle.
Monitor project expenditure across different cost categories and prepare cost reports, including variance analysis and financial projections to support in accurate decision making by programme leadership and governance groups.
Track contractor payments and support financial analysis of same ensuring robust and accurate cash flowing of the Programme budget.
 Support the Contracts and Claims team in reviewing and monitoring the cost performance of all contractors engaged on the programme.
Assist in ensuring financial processes associated with capital and programme expenditure are implemented, support continuous improvement in financial reporting and cost control processes within programme and project governance structures.
 Promote and participate in the implementation and management of change.
Proactively identify inequities / inefficiencies in service administration and implement solutions to improve service delivery, in line with legislation and benchmarking against best practice structures.
Maintain a good understanding of internal and external factors that can affect service delivery including awareness of local and national issues that impact on own area of work.
Embrace change and adapt local work practices accordingly by finding practical ways to make policies work, ensuring team knows how to action changes.
Encourage and support staff through change processes. Standards, Regulations, Policies, Procedures &amp;amp; Legislation
Contribute to the development of policies and procedures for own area
Effectively discharge the day-to-day operations, including compliance with Financial regulations and all policies and procedure.
 Assess and analyse compliance with National and EU legislative obligations, and national policies and procedure.
 Ensure accurate attention to detail and consistent adherence to procedures and current standards within area of responsibility
Maintain own knowledge of relevant policies, procedures, guidelines and practices to perform the role effectively and to ensure standards are met by own team
Maintain own knowledge of relevant regulations and legislation e.g. Financial Regulations, Health &amp;amp; Safety legislation, Employment legislation, FOI Acts etc
Pursue continuous professional development in order to develop management expertise and professional knowledge
Adequately identifies, assesses, manages and monitors risk within their area of responsibility. 

What you need to apply:

QQI Level 8 qualification in Engineering, Architecture, or Surveying.
Experience in financial analysis, cost management, budgeting, forecasting, and financial reporting.
Experience working on large capital projects or within construction, infrastructure, or healthcare environments.
Strong analytical skills with advanced Excel, Power BI, and financial systems knowledge (ACONEX desirable).
Excellent stakeholder management, communication, and reporting skills.
Ability to manage multiple priorities, analyse complex datasets, and support strategic decision-making.
]]></description><salary><![CDATA[€80,676]]></salary><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Accountancy/Finance]]></category></job><job><title><![CDATA[Communication Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-26 12:50:55]]></date><referencenumber><![CDATA[1812]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1812&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Communication Manager 
 Team Horizon is seeking a Communication Manager in Dublin. The Communications Manager will support communications, stakeholder engagement, onboarding, and training for a redevelopment programme. Working with the PMO and programme leads, the role ensures stakeholders receive clear, timely communications and are prepared for organisational and operational changes.
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

What you will be doing:

Develop and deliver internal and external communication strategies and stakeholder engagement plans.
Prepare communication materials, briefings, reports, media responses, and public information.
Coordinate onboarding, training, and change communications across the programme.
Manage media relations, political briefings, public affairs, and crisis communications.
Build strong relationships with internal teams, government bodies, healthcare leaders, and external stakeholders.
Monitor emerging issues and provide strategic communications advice to senior leadership.
Support programme governance by coordinating meetings, communications, and reporting.Adequately identifies, assesses, manages, and monitors risk within their area of responsibility.

What you need to apply:

QQI Level 8 qualification in Engineering, Architecture, or Surveying.
Experience delivering communications strategies in healthcare, construction, or a similar environment.
Strong stakeholder engagement, media relations, campaign management, and content development experience.
Excellent communication, writing, organisational, and project management skills.
Ability to manage multiple priorities, lead change communications, and work effectively with senior stakeholders.
]]></description><salary><![CDATA[€79,877]]></salary><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Commercial]]></category></job><job><title><![CDATA[Quantity Surveyor Advisor]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-30 11:47:39]]></date><referencenumber><![CDATA[1813]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1813&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Quantity Surveying Advisor
Team Horizon is seeking a Quantity Surveying Advisor in Cork who will support the planning, procurement, commercial management, and delivery of healthcare capital projects, ensuring value for money, compliance with policies, and the successful delivery of high-quality, sustainable healthcare facilities.
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

What you will be doing:

Provide quantity surveying, procurement, and commercial advice for capital projects.
Support the planning, approval, procurement, and delivery of the Capital Programme.
Manage design team QS consultants, contractors, budgets, costs, and project timelines.
Prepare capital submissions, cost estimates, cashflow forecasts, and progress reports.
Ensure compliance with public procurement, financial regulations, health and safety, and statutory requirements.
Promote cost control, value for money, sustainable design, and green procurement.
Develop policies, guidance, cost databases, and reporting frameworks.
Advise on construction risk, whole-life costing, and energy-efficient infrastructure.
Work with multidisciplinary teams and engage effectively with internal and external stakeholders.
Support continuous improvement, governance, and achievement of strategic objectives.

What you need to apply:
Eligibility Criteria

Level 8 (or higher) qualification in Quantity Surveying accredited by the SCSI or RICS (or equivalent).
Registered, or eligible to register, as a Quantity Surveyor under the Building Control Act 2007.
Chartered membership (or eligibility) of the Society of Chartered Surveyors Ireland (SCSI) or Royal Institution of Chartered Surveyors (RICS).
Minimum 7 years' relevant Quantity Surveying experience in a contractor or consultancy environment.
Strong technical knowledge of construction, procurement, cost management, and public sector capital projects.
Demonstrated administrative, analytical, and project management capability.
Full health, good character, and access to transport for site travel.

Key Skills &amp;amp; Experience

Extensive experience in quantity surveying, cost control, procurement, and contract management.
Knowledge of healthcare estates, construction legislation, Building Regulations, Health &amp;amp; Safety, Fire Safety, and the Capital Works Management Framework (CWMF).
Experience managing capital budgets, project risks, and multidisciplinary teams.
Strong leadership, stakeholder management, negotiation, and communication skills.
Excellent planning, problem-solving, report writing, ICT, and organisational abilities.
Committed to delivering quality services, value for money, continuous improvement, and professional development.
]]></description><salary><![CDATA[€79,877]]></salary><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[QA BMR Reviewer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-06-30 14:40:16]]></date><referencenumber><![CDATA[1814]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1814&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA BMR Reviewer for an initial 12-month contract at our clients manufacturing site in Dublin. The role will report into the QP &amp;amp; QA Ops Manager and is responsible for production support, postproduction review (BMR) or a quality system (i.e. Triage, Document Change Control, document Annual Review, etc.)
 
 
Why you should apply:

Opportunity to join a fast paced manufacturing site and work with an established team of quality professionals who strive for excellence and high-quality performance results.

 
 
What you will be doing:

Review of Intermediate and Finished Product Batch Manufacturing Records and any other batch related documents for completion and accuracy.
Review of Critical Process Parameters (CPPs) of BMRs to ensure the filed processes are met.
Raise and support the completion of Triages, DCRs, CAPAs, Non-conformances and Change Controls.
Review, collate and submit the necessary documentation to support QP release of finished product in accordance with Annex 16.
BMR and Logbook issuance through SAP, POMs and One Vault systems.
Manage and perform BMR/Logbook control, reconciliation, archiving, retrieval and returns through Iron Mountain (IM) system.
Carry out and monitor established QA/GMP programs.
Responsible for the management of the retain system for samples and documents.
Provides assistance in departmental and regulatory audits.
Has the ability to train a colleague in a particular GMP procedure or related activity.
Participate in department initiatives and projects.
Represent the QA BMR review team in cross functional meetings and provide the current documents review status.

 
What you need to apply:

A third level qualification in a scientific discipline, preferably a B.Sc./M.Sc.
Pharmaceutical experience with good working knowledge of cGMP.
Strong knowledge of FDA/EMEA regulatory requirements.
Excellent organizational, communication and interpersonal skills.
Ability to set and maintain the highest standards.
Ensures compliance to procedures, policies and guidelines and adherence with cGMP regulations, company policies and guidelines at all times.
Always Demonstrates an ethos of Right First Time.
Must quickly become familiar with products and processes

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Supply Chain Project Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-01 16:21:14]]></date><referencenumber><![CDATA[1815]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1815&amp;Itemid=986]]></url><city><![CDATA[Remote]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Supply Chain Project Manager to play key role in supporting the design and deployment of a new operating model across our clients supply chain and manufacturing organization.
 
 
Why you should apply:

Join a company who strive to have a remarkable impact on people's lives across several key therapeutic areas – and are committed to operating with integrity.  
This is an exciting opportunity to contribute to a major transformation initiative that will help shape how the company executes across process, systems, and master data as the organization moves from design into implementation. 
This position is well suited for a collaborative, solutions-oriented project professional who thrives in a complex and evolving environment.

 
 
What you will be doing:

Lead and coordinate project activities related to deployment of the new supply chain operating model across multiple manufacturing sites. 
Develop and maintain detailed project plans, timelines, and action trackers to support successful execution within scope, schedule, and budget. 
Manage stakeholder relationships and expectations across Supply Chain, Manufacturing, PMO, IT/ Business Technology Solutions, and other cross-functional teams. 
Facilitate project meetings, track deliverables, and provide clear status updates, risks, issues, and dependencies to management and project teams. 
Ensure effective use of PMO tools, templates, and project management processes in alignment with companies expectations. 
Support deployment planning for process, systems, and master data workstreams. 
Monitor project performance, financials, and key milestones to ensure accountability and timely escalation of risks. 
Identify and implement opportunities to improve deployment efficiency, execution quality, and cross-functional collaboration. 
Support change management and continuous improvement activities related to the new operating model. 
Contribute to the ongoing development and enhancement of PMO practices and project execution standards. 

 
 
What you need to apply:

Bachelor’s degree in business, Engineering, Science, or a related field. 
6+ years of experience in project management, program management, supply chain, operations, or a related business environment. 
Ability and willingness to business travel as needed to support deployment activities across sites. 
Experience supporting complex cross-functional projects, ideally in a supply chain, operations, systems, or process deployment context. 
Strong working knowledge of project management tools and methodologies; MS Project and project risk assessment experience preferred. 
Excellent communication skills with the ability to clearly share updates, decisions, actions, and issues with minimal supervision. 
Strong stakeholder management and collaboration skills across diverse teams and functions. 
Demonstrated ability to manage multiple priorities, deadlines, and deliverables in a fast-paced environment. 
Strong analytical and problem-solving skills, with the ability to think strategically and creatively. 
Financial acumen and ability to assess project performance and ROI. 

 ]]></description><jobtype><![CDATA[Remote, Contractor]]></jobtype><category><![CDATA[Supply Chain]]></category></job><job><title><![CDATA[Engineering Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-08 17:21:52]]></date><referencenumber><![CDATA[1817]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1817&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Engineering Manager for a leading pharmaceutical company in Sligo.
This position reports to the Operations Engineering Manager and is responsible for leading and managing a team comprising of engineers, technicians, and apprentices. The Engineering Manager support our API (Active Pharmaceutical Ingredients) business unit. 
Your role will involve team development, budget management, liaising with production and ensuring compliance with policies related to Personnel, Quality, Engineering, Safety and Finance.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

This is a varied position which requires cross-functional collaboration with contract maintenance providers, production, technical operations, quality and other personnel to ensure equipment performance is maximized. Your role will involve working on a variety of projects ranging from continuous improvement to new product introductions.
Establish in conjunction with the Operations Engineering Manager the department goals, schedules and timetables for activities. 
Assist with the management and support of manufacturing equipment development. 
Support the API Engineering Team in ensuring that manufacturing equipment is maintained to meet the required legal, divisional and corporate standards. 
Prepare appropriate CAPA plans and implement timelines. 
Undertake specific investigations, and equipment monitoring, with a view to improve manufacturing performance e.g., reducing plant downtime and maximizing Plant output and yield.   
Implementation of equipment/process upgrade in an environment of continuous improvement. 
Develop monthly engineering metrics and provide management reports in a timely manner. 
Ensure relevant budgets are within target and prepare capital expenditure requests for plant as required.
Ensure successful external, Division and Corporate audits. 
Ensure safety standards are met, and safe working practices are adhered to.  
Manage internal and external plant projects as needed. 
Supervise and manage relationships with external contractors. 
Attend relevant meetings and drive actions to closure. 
Any other duties as assigned.

 
What you need to apply:

Degree (Level 7 or above) in engineering or scientific area (Chemistry)
Minimum of 6 years pharmaceutical industry with a minimum of 2 years’ experience as an Engineering Supervisor.
Experience with glass lined vessels, reactors, pumps, heat exchangers, ATEX, solvent handling. High level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures.
Strong problem-solving skills with the ability to make prompt decisions on engineering related issues
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Fire prevention Officer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-09 17:27:24]]></date><referencenumber><![CDATA[1818]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1818&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Fire Prevention Officer for a company with sites in Dublin.
The Client provides a range of professional, technical, project management, property, fire &amp;amp; safety, and related services in respect of the procurement, development, operation, and maintenance of buildings, plant, and equipment. These services include design, specification, project management, supervision, and procurement associated with building and refurbishment works in the Dublin region.
 
Why you should apply:
●  They put their people first and live their diversity and inclusion values embracing all perspectives.
●  You enjoy working in a culture of learning and collaboration and making a positive impact.
 
What you will be doing:
●  The Fire Prevention Officer will be responsible, in respect of such premises and locations as may, from time to time be assigned to them for the following.
●  Advise on the suitability of equipment to reduce risks within the organisation, trying where possible to standardise products in consultation with the organisation Procurement Team.
●  Report as required to managers and relevant committees on areas of fire and infrastructural risk where action is required.
●  Receive copies of accident reports relevant to their area of expertise, and action/investigate, if necessary. Providing accident investigation reports for accidents investigated
●  Be a member of the organisation’s Integrated Quality and Risk committee, and where necessary be co-opted onto other groups as necessary.
●  Monitor and report on the health and safety performance of external contractors engaged on Construction related activity on the organisation’s premises.
●  Assist in the setting up and amendment of Emergency Plans.
●  Provide an input into planning the expenditure in relation to Fire Safety by highlighting and prioritising essential works required.
●  Regular inspections of buildings, means of escape and all fire-fighting equipment and ensuring that all such equipment is properly located, well-marked, in good repair and in good working order.
●  Reviewing and, as necessary, drawing up of fire orders, including evacuation schemes for the various types of building and institution, including schemes for evacuation of all persons with particular regard to mentally ill and non-ambulant patients and to draw up fire plans of all the organisations buildings and premises in his / her area of responsibility.
●  Regular and routine inspection of places, premises and equipment, which present a special risk of fire and reporting any breaches of the fire prevention code.
●  Instruction of staff in each premises in: Avoidance of fire hazards, Summoning of the fire brigade, Operation of the fire alarm and fire equipment, and means of escape.
●  Curtailment of an outbreak of fire, pending the arrival of the fire brigade, prevention of smoke spread and evacuation of danger areas.
●  Arranging regular fire drills in each location and ensuring that they are properly carried out.
●  Monitoring, by having regular tests carried out, the water supply in all divisions of each institution, to ensure that it is of sufficient volume and pressure for firefighting purposes and reporting any deficiencies in this regard.
●  Ensuring that all hydrants are clearly identified.
●  Advising as appropriate regarding interpretation of Fire Protection Standards and Building Regulations issued by the Government Departments and ensuring their implementation.
●  Monitoring all means of escape to ensure that they are always both safe and adequate and, kept operative and clearly indicated.
●  Keeping proper records of all inspections, fires, evacuation drills, fire-fighting equipment and such other matters relating to his/her office as Fire Prevention Officer.
●  Reporting in writing, to the Engineering Manager, at three-monthly intervals on the state of the fire prevention services in the organisation buildings and premises assigned to him/her. Also, report immediately all outbreaks of fire, breach of the fire prevention order and failure to perform fire drill at the Organisations buildings and premises. If so directed, the Fire Safety Officer will make out an annual report on all aspects of fire and safety pertaining to the organisation’s property in their area of responsibility.
●  Arrange to have the fire prevention work programmes implemented under the direction of the Engineering Manager.
●  Monitor and report on the management of Health Safety and Infrastructural Risk issues of the organisation.
●  Assess the continuous professional training requirements for staff in the area and advise the Engineering Manager of the appropriate training courses and coordinating with the training providers on the course provided.
●  Engage in the organisation’s performance achievement process in conjunction with your Line Manager and staff as appropriate.
●  Monitor the performance and implementation of the organisations Safety Management programme by regular spot checks, by analysis of safety audit reports and accident and incident returns.
●  Act as an information source and resource to management and staff on fire safety, general safety, health and welfare matters.
●  Advise, guide and participate in the risk assessment process/inspection within the area of fire maintenance and infrastructural risk.
●  Assist in the development of health and safety training programmes for maintenance staff which are to be harmonised throughout the company.
●  Adequately identifies, assesses, manages and monitors risk within their area of responsibility.
●  Support, promote and actively participate in sustainable energy, water and waste initiatives to create a more sustainable, low carbon and efficient health service.
●  Achievement of targets and plans and completion of agreed programme within allocated budget.
●  Act as spokesperson for the Organisation as required.
●  Demonstrate pro-active commitment to all communications with internal and external stakeholders
●  Develop good working relationships with other members of the team and with administrators of institutions in which maintenance staff are engaged
 
What you need to apply:
●  Hold a HETAC level 7 qualification (NQF) in engineering, fire engineering, architecture, Health and Safety or Building Services/Building Survey. Or hold an equivalent qualification.
●  Have two years’ experience in comparable Fire and Safety role.
●  And Have a high degree of proficiency / expertise in Microsoft office.
 ]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Site Automation Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-16 09:22:02]]></date><referencenumber><![CDATA[1819]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1819&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Site Automation Manager 
 Team Horizon is seeking a Site Automation Manager for a client in Cork. The Automation Manager will lead the Automation and MES team within the Engineering department, directly reporting to the Site Engineering Manager. In this role, you will maximize manufacturing system efficiency by leveraging advanced automation technologies and fostering a culture of operational excellence and people development. 
 Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Deliver maximum availability and performance of automation and MES solutions, using proactive/predictive maintenance to minimize downtime.
Oversee design, implementation, and full lifecycle management of automation/MES projects, ensuring efficient and cost-effective manufacturing aligned with business priorities.
Drive digital transformation and paperless manufacturing initiatives leveraging expert technical skills.  Lead, coach, and develop a high-performing team; provide mentoring, feedback, performance reviews, and clear objectives.
Foster a collaborative and inclusive team culture focused on learning, accountability, and knowledge sharing.
Champion process enhancements and embed automation best practices for continuous improvement.
Recognize and reward innovation; lead and support change management initiatives as technologies and business needs evolve.
Build strong, trust-based relationships with cross-functional stakeholders, aligning automation strategy with business needs.
Maintain the highest standards in communication, customer focus, and stakeholder engagement internally and externally.
Ensure compliance with cGMP, SOPs, data integrity and security, and Health, Safety &amp;amp; Environmental regulations.
Promote an EHS&amp;amp;E culture, set ISO and company standards, and always demonstrate a ‘Right First Time’ ethos.

 What you need to apply:

Degree (Level 8) in Automation, Electronic Engineering, or a related discipline.
Minimum 10 years of technical experience in the Pharmaceutical industry, focused on automation and MES systems.
Extensive knowledge of pharmaceutical equipment; experience with solid dosage or sterile manufacturing preferred.
At least 5 years of proven project and people management experience, with a strong track record of talent development and results delivery. 
Inspirational leadership style, proactive change management skills, and a passion for continuous improvement. 
Excellent leadership, decision-making, and communication abilities. 
Strong customer focus and proven collaborative team player. 
Fluent English, both written and oral.
]]></description><salary><![CDATA[€100,000]]></salary><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[CQV Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-16 12:23:37]]></date><referencenumber><![CDATA[1820]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1820&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CQV Engineer for a leading pharmaceutical company in Athlone.
We are seeking an experienced CQV Engineer to manage commissioning and qualification activities for utilities, equipment, and process systems. It’s a short term contract role
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Athlone.

 
 
What you will be doing:

Lead the CQV strategy for the facility upgrades, ensuring alignment with project goals and regulatory requirements.
Develop and maintain the CQV master plan, protocols, and schedules.
Coordinate cross-functional teams including engineering, quality, manufacturing, IT, automation and project management.
Manage commissioning and qualification activities for utilities, equipment, and process systems.
Ensure timely execution of IQ/OQ/PQ protocols and documentation.
Drive resolution of CQV issues, deviations, and change controls.
Ensure adherence to GMP, FDA, EMA, and other applicable regulatory standards.
Maintain accurate and audit-ready CQV documentation.
Support regulatory inspections and internal audits.
Act as the primary CQV point of contact for project stakeholders.
Provide regular updates on CQV progress, risks, and mitigation strategies.
Collaborate with vendors and contractors to ensure CQV deliverables are met.
Any duties as assigned.

 
What you need to apply:

Bachelor’s or Master’s degree in Engineering (Mechanical, Chemical, Biopharmaceutical, or related field).
Minimum 5 years of experience in C&amp;amp;Q within the Life Sciences industry.
Strong knowledge of regulatory guidelines (FDA, EMA, ISPE, GAMP).
Hands-on experience with risk-based qualification and C&amp;amp;Q protocols.
Strong problem-solving, communication, and teamwork skills. Experience working on large-scale capital projects is a plus.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[CQV Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-16 12:23:37]]></date><referencenumber><![CDATA[1820-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1820&amp;Itemid=986]]></url><city><![CDATA[Westmeath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CQV Engineer for a leading pharmaceutical company in Athlone.
We are seeking an experienced CQV Engineer to manage commissioning and qualification activities for utilities, equipment, and process systems. It’s a short term contract role
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Athlone.

 
 
What you will be doing:

Lead the CQV strategy for the facility upgrades, ensuring alignment with project goals and regulatory requirements.
Develop and maintain the CQV master plan, protocols, and schedules.
Coordinate cross-functional teams including engineering, quality, manufacturing, IT, automation and project management.
Manage commissioning and qualification activities for utilities, equipment, and process systems.
Ensure timely execution of IQ/OQ/PQ protocols and documentation.
Drive resolution of CQV issues, deviations, and change controls.
Ensure adherence to GMP, FDA, EMA, and other applicable regulatory standards.
Maintain accurate and audit-ready CQV documentation.
Support regulatory inspections and internal audits.
Act as the primary CQV point of contact for project stakeholders.
Provide regular updates on CQV progress, risks, and mitigation strategies.
Collaborate with vendors and contractors to ensure CQV deliverables are met.
Any duties as assigned.

 
What you need to apply:

Bachelor’s or Master’s degree in Engineering (Mechanical, Chemical, Biopharmaceutical, or related field).
Minimum 5 years of experience in C&amp;amp;Q within the Life Sciences industry.
Strong knowledge of regulatory guidelines (FDA, EMA, ISPE, GAMP).
Hands-on experience with risk-based qualification and C&amp;amp;Q protocols.
Strong problem-solving, communication, and teamwork skills. Experience working on large-scale capital projects is a plus.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-16 12:25:41]]></date><referencenumber><![CDATA[1821]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1821&amp;Itemid=986]]></url><city><![CDATA[Roscommon]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer for a leading pharmaceutical company in Athlone.
The Project Engineer will lead the equipment purchase, delivery installation and qualification of the processing equipment on site. Overseeing, leading and supporting the work of the other project engineers. 
New Processing equipment with some Facility / utilities modifications to incorporate same.
 
Why you should apply:
●  Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
●  You enjoy working on exciting projects and want to work with a global manufacturing site in Athlone
 
What you will be doing:
●  Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. 
●  Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel.
●  Writing User Requirement Specifications.
●  Selecting Vendors and completing Vendor evaluation matrix.
●  Managing contractors and project schedules.
●  Writing RCE's, placing orders, Project Management &amp;amp; Design review meetings.
●  Lead the Project Team participation in Factory Acceptance Testing program.
●  Coordination of all equipment documentation requirements.
●  Commissioning of equipment and Engineering support during qualification.
●  Work with the E&amp;amp;T Senior Manager &amp;amp; System Owner / Project Team.
●  Handover training, coordination of O&amp;amp;M manuals, Spare parts, &amp;amp; PM schedules.
●  Lead your regular weekly / bi-weekly Project review meetings with your Project team.
 
What you need to apply:
●  Third level qualification in an Engineering or equivalent discipline/experience.
●  Experience of working in Biologics, Pharmaceuticals or Medical device industry.
●  Min of 3 to 5 years’ experience in sterile filling/manufacturing process.
●  Project management experience with proven record.
●  Assured self-starter with proven technical ability.
●  Good communication and interpersonal skills required to operate in a multi-function project team set up.
●  Ability to work within a team using your own initiative to articulate and deliver specific functional requirements for all aspects of the project and work with members of various disciplines and functions across the project.
●  Good team leading skills and ability to work closely with other areas/departments within an organization.]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-16 12:25:41]]></date><referencenumber><![CDATA[1821-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1821&amp;Itemid=986]]></url><city><![CDATA[Westmeath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer for a leading pharmaceutical company in Athlone.
The Project Engineer will lead the equipment purchase, delivery installation and qualification of the processing equipment on site. Overseeing, leading and supporting the work of the other project engineers. 
New Processing equipment with some Facility / utilities modifications to incorporate same.
 
Why you should apply:
●  Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
●  You enjoy working on exciting projects and want to work with a global manufacturing site in Athlone
 
What you will be doing:
●  Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. 
●  Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel.
●  Writing User Requirement Specifications.
●  Selecting Vendors and completing Vendor evaluation matrix.
●  Managing contractors and project schedules.
●  Writing RCE's, placing orders, Project Management &amp;amp; Design review meetings.
●  Lead the Project Team participation in Factory Acceptance Testing program.
●  Coordination of all equipment documentation requirements.
●  Commissioning of equipment and Engineering support during qualification.
●  Work with the E&amp;amp;T Senior Manager &amp;amp; System Owner / Project Team.
●  Handover training, coordination of O&amp;amp;M manuals, Spare parts, &amp;amp; PM schedules.
●  Lead your regular weekly / bi-weekly Project review meetings with your Project team.
 
What you need to apply:
●  Third level qualification in an Engineering or equivalent discipline/experience.
●  Experience of working in Biologics, Pharmaceuticals or Medical device industry.
●  Min of 3 to 5 years’ experience in sterile filling/manufacturing process.
●  Project management experience with proven record.
●  Assured self-starter with proven technical ability.
●  Good communication and interpersonal skills required to operate in a multi-function project team set up.
●  Ability to work within a team using your own initiative to articulate and deliver specific functional requirements for all aspects of the project and work with members of various disciplines and functions across the project.
●  Good team leading skills and ability to work closely with other areas/departments within an organization.]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Maintenance/Engineering Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-16 14:32:43]]></date><referencenumber><![CDATA[1822]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1822&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking Maintenance Technicians for a leading pharmaceutical companies in Blanchardstown, Dublin. This role involves shift work on a 4 week cycle.
Responsible for the set up and maintenance of automated vial and syringe filling equipment. Responsible for maintenance and repair of plant equipment and utilities.
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Dublin

 
What you will be doing:

Responsible for Setup, planned maintenance and fault finding of automated Vial and Syringe filling equipment.
Responsible for maintenance of equipment and utilities and documenting work to a GMP standard.
Manage external contractors when required during equipment installations and planned service visits.
Manage spare parts, consumables, and services to keep equipment schedules compliant.
Develop, Implement, and promote a Reliability Centered Maintenance (RCM) strategy using Failure Mode Effects and Criticality Analysis (FMECA/FMEA) assessments in conjunction with department management, the Engineering dept reliability engineer and the Production department utilizing tools such as Trend’s analysis &amp;amp; Control charts &amp;amp; Data review.
Support the creation and modification of documentation to support maintenance and calibration activities (PM, Data Sheets, Work Instructions, troubleshooting guides).
Support compliance efforts related to Safety Events, Quality Events, CAPAs, change management and investigations and assist in the investigation and resolution of electrical and mechanical issues on equipment.
Ensure maintenance routines, procedures, and work plans are developed to the necessary standards and best practice to ensure compliance with cGMP and EHS regulations.
Comply with cGMP &amp;amp; EHS requirements from a local, global, and regulatory perspective.
You will be required to be flexible in this position and must be prepared to such undertake overtime; shift cover, on call and other works as may be assigned to your role by the company.
All other duties as requested or assigned.

 
What you need to apply:

Minimum of a Certification in Electrical/Mechanical Engineering and a minimum of 5 years relevant experience. However, a combination of experience and education will be taken into consideration. Excellent Interpersonal / Communication skills Conflict management / Negotiation.
Structured decision making. Computer literacy (Word, Excel, PM systems). Report preparation &amp;amp; presentation.
Ability to manage multiple projects and activities simultaneously. Proven analytical and problem-solving skills.
Ability to read and interpret general business documents and to compile Technical reports.
Ability to work with peers and communicate.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Operations Lead ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-20 17:19:44]]></date><referencenumber><![CDATA[1823]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1823&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking an Operations Lead for a pharmaceutical client in Dublin. The Operations Lead will serve as primary production process owner responsible for New Production Introduction, life cycle management projects and or CAPEX projects and established process improvements projects.
 
This role requires in depth technical and operational knowledge of aseptic drug product manufacturing processes; parts/ components preparation, formulation, syringe filling, vial filling, lyophilisation and capping.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Function as the site interface between the Product Delivery Teams (PDT’s), and ADL Manufacturing operations.
Engaging with staff members within the Manufacturing department to ensure understanding of the processes and working collaboratively cross functionally with Facilities &amp;amp; Engineering, Quality, PD and Supply Chain.
Develop, review, and approve Generic Master Batch Records and Parameter Value Lists across Formulation, Filling and Inspection.
Develop, review and update Production, Engineering, Operating Procedures &amp;amp; training materials
Assist in providing training on scientific or technical aspects of the current process/project(s) to Direct Manufacturing.
Evaluate, plan, and implement solutions for process improvement opportunities both current and project related.
Support scheduling and execution of Characterisation, Engineering and PPQ runs, ensuring all necessary pre-requisites are included on the schedule and assess process performance by observation of floor operations and review of performance data
Provide troubleshooting support throughout the project and on the floor during execution of activities
Hold people to account for delivery and behaviors within the Manufacturing Support team and associated with the project(s)
Perform Job Hazard Assessments and Change Control Assessments to determine impact to Manufacturing.
 Partner with Learning &amp;amp; Performance to define training strategies for current processes, NPIs and complex projects.
Consult with Quality Assurance to ensure that GMP standards are maintained in line with current SOP’s, batch documentation and licence.
 Develop, review and update Protocols for manufacturing activities.
Documentation and approval of protocol deviations for manufacturing activities
Consult with Process Development, Direct manufacturing, Equipment, and System Owners regarding process changes in an effective and timely manner
 Own and lead change controls as required by the Manufacturing support team
Review and approve Bills of Materials.
Develop, review and update Product Quality Risk Assessments.

 
What you need to apply:

Bachelor’s degree in a science discipline.
3+ years of biopharmaceutical manufacturing experience in Fill Finish or related manufacturing or GMP experience in the pharmaceutical or medical device industry.
Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
Strong Project Management and organizational skills, including ability to follow assignments through to completion
Critical thinking skills: Gathers data from key stakeholders, analyses and interprets information to develop solutions to technical problems of moderate complexity
Negotiation and Influencing skills
Take initiative to identify and drive improvements
Excellent verbal and written communication skills: Strong Technical writing skills for GMP documentation (e.g., investigations, procedures, change controls) and good Presentation skills
Escalate issues professionally and in a timely manner
Decision Making skills and confidence to challenge others on decisions that impact the manufacturing area
Teamwork and Coaching others
Ensures compliance within regulatory environment
Demonstrated ability to work independently and deliver right first-time results under minimal direction

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Drug Product Technical Operations ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-22 12:18:58]]></date><referencenumber><![CDATA[1827]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1827&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Drug Product Technical Manager for our client based in Sligo. This role provides technical expertise in chemistry and chemical engineering, alongside program management support for commercial DP manufacturing and site-wide NPI delivery. The position also plays a key role in monitoring processes and identifying opportunities to improve yield, reduce cycle times, and lower standard product costs through continuous improvement.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Manage a team of 3–6 direct reports.
Set annual goals, complete reviews, and own growth plans and performance management.
Provide cross-training, mentoring, and guidance to team members.
Operate with significant autonomy while aligning with the Technical Operations Manager
Own technical accountability for 4–6 commercial and NPI products involved in large-scale drug product manufacture.
Provide support for highly complex processes, including chemistry, engineering, and solid oral dose technical requirements.
Lead all new process and validation activities from project start-up through process qualification. Identify, prioritise, and manage continuous improvement projects; coach technical support engineers and chemists; and coordinate with cross-functional teams.
Prepare process fits, feasibility studies, development work, and operating budgets for future product introductions.
Plan and lead technical transfers for future product introductions.
Support departmental budgeting as delegated by the Manufacturing Manager.
Manage medium-scale capital projects.
Support site strategy and work with internal and external stakeholders to influence product development and transfer.
Promote company culture within the team and across the department.
Adhere to all EHS &amp; E standards, procedures, and policies.

 
What you need to apply:

Bachelor’s degree in a relevant science or technical discipline. People leadership experience with experience managing direct reports.
5+ years’ experience in process chemistry or process engineering within a GMP pharmaceutical environment.
3–5+ years’ experience supporting start-ups and/or new product introductions in pharmaceutical facilities.
Experience in batch processing, technical transfers, commissioning, and validation.
Strong problem-solving skills under pressure, with the ability to assess multiple solutions.
Innovative thinker with a track record of proposing, demonstrating, and implementing new solutions. High attention to detail, strong compliance mindset, and a results-driven approach.
Strong communication and interpersonal skill

 
 ]]></description><salary><![CDATA[Upto £10,000]]></salary><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Senior Electronic Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-22 16:02:25]]></date><referencenumber><![CDATA[1828]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1828&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Senior Electronic Engineer
Team Horizon is seeking a Senior Electronic Engineer for a client in the automotive industry in Galway. This person will join dynamic engineering team responsible for the design, development, validation, and delivery of innovative electronic products.
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

Lead the design, development, and validation of complex electronic hardware solutions.
Take ownership of electronic engineering deliverables throughout the project lifecycle.
Plan, monitor, and manage engineering activities to ensure successful project delivery.
Review customer requirements, technical specifications, and internal design requirements.
Design and review electronic schematics and high-density PCB layouts.
Perform design calculations, simulations, testing, and validation activities.
Support board bring-up, hardware debugging, and product verification.
Ensure designs comply with engineering standards, design rules, and manufacturing requirements.
Lead technical design reviews and ensure timely resolution of technical issues.
Collaborate with firmware, software, mechanical, manufacturing, and quality teams.
Support Design for Manufacturing (DFM), Design for Test (DFT), and product compliance activities.
Interface with customers on technical matters where required.
Identify technical risks and escalate issues appropriately.
Mentor and provide technical guidance to junior engineers and technicians.
Support project planning, scheduling, and resource management.

What you need to apply:

8–10+ years' experience in electronic hardware design and product development.
Proven experience delivering electronic products from concept through to production.
Experience leading technical projects or acting as a senior technical contributor.
Experience working within multidisciplinary engineering teams.
Simulation, schematics and zuken would skills would be an advantage
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Quality Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-28 15:32:10]]></date><referencenumber><![CDATA[1829]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1829&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Quality Assurance Technician to join a team to support a Product Transfer project. This is a 12-month contract with potential for extension and move to Quality &amp;amp; Operations once project is finished.
 
 
Why you should apply:

Opportunity to join a fast paced manufacturing site and work with an established team of quality professionals who strive for excellence and high-quality performance results.

 
 
What you will be doing:

Work as a member of the Quality Team to ensure that Quality goals and objectives are achieved.


Ensure that all actions comply with current good manufacturing practices.
Operate within the QC/ IQA and Metrology Areas, as required.
Complete incoming product testing with the relevant approved specifications and procedures.
Complete in-process and final release product testing with the relevant approved specifications and procedures.
Ensure Management is kept informed of all Quality Events or potential Quality Events Related to the product or process.
Ensure all Quality System documentation is thorough, complete, and compliant.


Audit the quality system with other personnel where required.
Support Change Management Process including Product and Quality System document review and updates.
Generate and Providing metrics for inclusion in the management review, monthly reports and overall Quality Performance
Ensure compliance with training requirements is maintained.
Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems at the site.
Generate batch records for as required in support of manufacturing process orders.
Complete disposition decisions for incoming material

 
What you need to apply:

A third level qualification in an appropriate discipline is desirable.
2+ years’ Experience within a regulated GMP environment
Experience in the day-to-day operation of the quality system in a highly regulated combination product/device manufacturing environment is desirable.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[Continuous Improvement Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-07-30 14:14:27]]></date><referencenumber><![CDATA[1830]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1830&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Continuous Improvement Specialist
Team Horizon is seeking a Continuous Improvement Specialist for a client in Dublin. The Continuous Improvement Specialist is a key member of the Continuous Improvement and Industrial Engineering team. The role acts as the CI business partner for assigned areas, supporting deployment and sustainment of improvement routines in line with the site's management system.
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

Support assigned areas in daily management, standard work, structured problem solving, process confirmation, and improvement routines.
Independently facilitate problem-solving sessions, workshops, and improvement activities with cross-functional groups.
Coach Yellow Belt and Green Belt candidates, project sponsors, process owners, and team members on improvement tools, project governance, and sustainment.
Promote productivity ideation and CI culture by identifying, scoping, proposing, and initiating improvement opportunities aligned with business priorities.
Deliver assigned improvement projects from problem definition through implementation, benefit validation, control planning, and sustainment.
Use data analysis to accelerate problem solving, understand KPI performance, identify drivers, and quantify improvement opportunities.
Partner with Industrial Engineering colleagues to understand relevant capacity models and use capacity insight to identify opportunities and quantify improvements.
Liaise with CI and Business Performance Specialists to ensure valuable operational KPIs are reflected in digital dashboards and related performance tools.
Support rapid process analysis and improvement using appropriate digital, automation, and AI-enabled tools where practical.
Complete any other tasks or projects assigned by the Continuous Improvement and Industrial Engineering Lead for AD

What you need to apply:

Bachelor's degree in Engineering, Science, Business, Manufacturing, Operations, Quality, Supply Chain, or related field.
3–5+ years' experience in Continuous Improvement, Operational Excellence, Lean Manufacturing, Process Improvement, or Project Delivery.
Hands-on Lean and/or Six Sigma project experience (certification desirable but not essential).
Experience with structured problem-solving methods (DMAIC, A3, RCA, Kaizen).
Strong data analysis skills with advanced Excel; Power BI, SQL, or Power Query is an advantage.
Experience facilitating cross-functional teams and driving improvement initiatives.
Knowledge of daily management, standard work, and Lean tools.
Experience in pharmaceutical, GMP, or regulated manufacturing is preferred.
Strong stakeholder management, communication, coaching, and change management skills.
Ability to manage multiple projects and deliver sustainable business improvements.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Tech Transfer Leads (Intermediate)]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-04 10:57:19]]></date><referencenumber><![CDATA[1832]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1832&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Tech Transfer Leads (Intermediate) for our client based in Dublin. This role will require the candidate to provide process development support primarily to new product introductions (NPI) and lifecycle management (LCM) changes.. In addition, the candidate will be expected to provide technical support to biologics drug product manufacturing as part of the global Process Development organization. With the intention of moving to a new building construction that will house single use end to end processes and new syringe fillers.
 
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Development of documentation and process design for characterisation studies, engineering runs, electronic batch record creation, validation plans, process performance qualifications for syringe filling.
Ensuring all aspects of activity within any given process validation adheres to required policies and procedures, including safety and training.
Ensure that the site meets the quality requirements of its customers and applicable regulations (FDA, EU &amp;amp; international standards) with a full understanding of CMC business process related to technology transfer.
Participate in process validation cross functional teams at the site to ensure adherence to required policies and procedures and be responsible to deliver against organizational goals and project milestones.
Pre-approve and post-approve process validation protocols and assessments from a quality system documentation perspective.
Actively communicates across functions and sites and is a strong collaborator with all the functional groups at the receiving site, sending site and corporate functions.
Act as the responsible point contact from site for the transfer project for drug product teams and Global Operations Teams.
Assist in the development of any existing validation program to ensure continued compliance to the necessary regulations and input to site validation guidance documents.
Collate and report on relevant shipping and filter validation.
Assist in deviation and exception resolution and root cause analysis.
Contribute to product quality assessments and process flow documents.

 
What you need to apply:

Third level Bachelor’s degree in science, engineering or equivalent discipline with 4 years experience in a commercial manufacturing or NPI role OR Master’s degree &amp;amp; 2 years of directly related experience OR Associate’s degree &amp;amp; 7 years of directly related experience.
Strong technical writing skills.
Knowledge of cGMPs and other worldwide regulatory requirements.
Problem solving ability and excellent oral and written communications skills.
Experience in support of Commercial Protein Drug Product (DP) processing in specific areas such as sterile processing, process characterization, tech transfer (to commercial DP sites) or validation.
Strong skills in applying fundamental engineering and scientific principles to the design, implementation and process validation of protein freeze-thawing, filtration, mixing, filling (PpK / batch homogeneity).
Knowledge of protein biochemistry with regard to chemical and physical stability.
Project management skills including the ability to manage multiple projects and evaluate project resource requirements
Strong knowledge of Quality systems, Drug Product Manufacturing and Validation.
Demonstrated ability in providing leadership to cross-functional teams to advance complex projects to completion.
Excellent Communication skills are essential for this role.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Global Quality Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-04 15:14:55]]></date><referencenumber><![CDATA[1834]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1834&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Global Quality Specialist for an initial 12-month contract with a Client in Dublin.
 
 
Why you should apply:

Join a team who unleash bold thinking with the power to inspire life-changing medicines.
Hybrid role with a mix of in-person working to give a platform to connect, work at pace and challenge perceptions with balance of remote working 2 days per week.

 
 
What you will be doing:

Supporting the Medical Device Quality Team in progressing the update and release of documents &amp;amp; records in the document management system.
Supports Combination Product Audit readiness initiatives and support during audits.
Supports Notified Body and Health Authority inspections and compliance.
Responsible for collection/collation of QMS data and performing data analysis to support periodic Combination Product Management Review reports, meetings, minutes and actions.
Supporting weekly/monthly/quarterly QMS governance reporting.
Support cross functional teams with review board meetings (e.g. Change control, Supplier Change, change planning, Standards review planning, risk review) and Supplier Quality Agreement updates. Supporting action includes coordination of review meetings including documenting minutes &amp;amp; actions and filing of records.
Ensure timely entry, processing, and closure of quality records in compliance with procedures.
Attending site team meetings relating to operations activity to ensure quality compliance for combination products.
Support Deviation / CAPA processes by providing oversight of content for compliance, supporting owners in initiating CAPAs and completing action tasks per SOPs to completion on time.
Support change control initiators to ensure change control documentation meets combination product  regulations per SOPs.
Ensure change control documentation including impact assessments are ready and adequate for approval at Change Control Review Board.
Liaise with third parties such as device constituent partner manufacturers related to device related investigation outcomes and root cause assessments.
Partner with Quality partners to maintain and improve the  combination product Quality Management System.
Communicate effectively, both verbally and in writing, internally across departments and with external partners.
Comply with the quality assurance requirements as well as applicable regulatory requirements.
Other duties as assigned.

 
What you need to apply:

Minimum of a bachelor’s degree or equivalent experience in a regulated industry.
Knowledge of the regulatory and compliance requirements for medical devices and/or combination products (e.g. FDA QMSR 21 CFR Part 820 and Part 4 / ISO 13485 and Regulation (EU) 2017/745), ISO 14971.
Experience using electronic QMS / document management systems (e.g., Veeva Vault) for document lifecycle, quality events, and action tracking.
Demonstrated experience managing quality or compliance- related projects in a regulated medical device and/or combination product environment. 
Proven ability to plan, track, and deliver projects while maintaining focus on compliance, quality, and timelines.
 Experience applying a structured, risk based approach to continuous improvement within a Quality Management System.
Excellent communication and interpersonal skills
Knowledge of quality systems with a strong technical acumen would be an advantage.
Preferable 4 years +’ cGMP experience within quality in a medical device, combination product R&amp;amp;D or manufacturing environment.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality]]></category></job><job><title><![CDATA[ADC Process Scientist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-13 16:30:16]]></date><referencenumber><![CDATA[1835]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1835&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a ADC Process Scientist for a leading pharmaceutical company in Sligo.
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Sligo.

 
What you will be doing:

Leverage detailed understanding of the science behind antibody drug conjugate (ADC) manufacturing and the manufacturing process as manufacturing plant-based Process Scientist SME for technology transfers and ongoing manufacturing.
Work with Research &amp;amp; Development and Drug Product Development functions to develop and transfer a well understood, robust, fit-for-purpose process control strategy for each new product introduction (NPI).
Author gap assessments, facility fit studies, process safety and risk assessments for NPI.
Design, onboarding, and testing of single use assemblies for use in sterile manufacturing of ADC.
Process SME for equipment selection and C&amp;amp;Q activities for any new equipment.
Author scientific reports and technical documentation and presentations to document and communicate project status to internal and external stakeholders.
Understand and ensure compliance with safety, regulatory and compliance expectations.
Other duties as assigned.

 
What you need to apply:

Graduate degree in Chemistry, Biochemistry, Analytical Science or related discipline with 3-5 years experience (MSc) or 2-5 years experience (PhD) in biopharmaceutical industry.
Experience with at scale ADC manufacturing including conjugation and fill finish operations.
Detailed understanding of the chemistry of large molecule and protein conjugation as evidenced by successful project execution
Desirable: Experience with new product introductions / technology transfers to fill finish manufacturing facility.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific]]></category></job><job><title><![CDATA[Clerk Of Works]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-20 09:26:16]]></date><referencenumber><![CDATA[1838]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1838&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Clerk of Works for a building and refurbishment construction projects in Cork.
To work as part of a multidisciplinary team to ensure that Construction Projects being delivered are of sufficient quality at handover, along with providing assistance to Engineers specifically regarding site works. 
The Clerk of Work Plays a crucial role in Construction Management, ensuring that mechanical ( e.g., HVAC, Plumbing, and Fire Protection Systems) and Electrical (e.g., power distribution, lighting and IT communications wiring) components are specified, Co- Ordinated, and installed according to project specifications.
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

To report to and take instructions from the Design Team and the Project Manager. To liaise as necessary with the Maintenance Manager. The Clerk of Works will have no authority to modify the design, incur additional costs or approve samples.  Moreover, he/she will have no authority to direct the main contactors methods of work or be empowered to issue variations from the contract documents.
To assist in the correct interpretation of all documents and to ensure that all works are carried out in accordance with the drawings, specification and other contract documents.
To advise the Design Team of any additional information required by the contractor.
To check that all workmanship and material meet the standards and performance criteria for the project and to identify and record unacceptable work as soon as possible for the information of the Architect/Design Team accordingly.
Implement Permit-to-Work procedures and co-ordinate with relevant staff the management of interfacing shutdowns, connections and commissioning of services and building works under the contract, reporting to the Architect and the Estates Department as necessary.
To report to the Design team on the implementation of the main contractors programme for the works, preparing progress reports, keeping records of instructions, variations and day works.
To record any factors that could give rise to claims for disruption or affect the projects progress.
To assist the Design Team in site inspections.
To identify and maintain an up to date schedule of remedial items.
To accompany all Local Authority Inspectors on their visits to site, maintaining the necessary liaison with the Local Authorities, as appropriate, in respect of compliance with statutory requirements.
To attend Design Team meetings, both on and off site, and site meetings as required.
To keep a detailed accurate diary of all events pertaining to the job, to include site reports, recording progress, material delivery and site labour and plant. Diary to be prepared in a form to be agreed with the Employers Representative (Architect).
Attend meetings arranged by the Engineering Department as required and furnish such reports as required.
Project Coordination: Work closely with project managers, architects, and engineers to review all design plans, specifications, and drawings.
Conduct in situ / above ceiling surveys to ensure that all new  wiring and containment installations meet design, safety, and quality requirements.
Ensure that M&amp;amp;E systems are designed and installed in accordance with the design documents and that containment can be installed in a coordinated manner with existing systems and building fire compartmentalisation.
Coordinate with subcontractors to ensure the scheduled installation of systems throughout a building campus or standalone buildings.
Witnessing of S/N testing of new  installations.
Compiling Handover and “As built” documentation for the various projects.
Constructability Reviews &amp;amp; Compliance: Review and interpret technical service routing drawings (mechanical, electrical, plumbing) to ensure compliance with the project’s design intent, building codes, and industry standards.
Identify potential conflicts between M&amp;amp;E systems and structure and resolve them before installation.
Ensure compliance with local regulations, codes, and safety standards.
On-site Supervision: Oversee the installation of all systems on-site to ensure quality and adherence to specifications.
Communication &amp;amp; Liaison: Act as the point of contact between the project team, subcontractors, and clients for all -related issues.
Facilitate coordination meetings to ensure that all parties are aligned on design changes, timelines, and expectations.
Problem-solving &amp;amp; Troubleshooting: Proactively identify potential problems with mechanical or electrical systems before they occur.
Troubleshoot issues during the construction phase, ensuring they are resolved quickly to avoid project delays.
Documentation &amp;amp; Reporting: Maintain up-to-date records of designs, specifications, and installation progress.
Prepare reports on project status, key issues, and milestones for the project management team.

 
What you need to apply:

Have attained a reasonable standard of general education commensurate with the role and have a satisfactory knowledge of and experience of duties to be performed and be capable of working on his/her own initiative.
Applicants must have served a recognized apprenticeship in a building or construction craft.
Have five years satisfactory supervisory and practical experience of complex building projects.
Possess the requisite knowledge of construction contract procedures and be capable of writing clear and precise reports, keeping work records, measuring and recording all variations from contracts and reading drawings.
Knowledge of and ability to interpret architects/engineers’ drawings, specifications and technical directions.
Have a high standard of practical experience in building construction.
Have a high degree of proficiency / expertise in Microsoft office.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Clerk Of Works]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-20 09:26:16]]></date><referencenumber><![CDATA[1838-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1838&amp;Itemid=986]]></url><city><![CDATA[Kerry]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Clerk of Works for a building and refurbishment construction projects in Cork.
To work as part of a multidisciplinary team to ensure that Construction Projects being delivered are of sufficient quality at handover, along with providing assistance to Engineers specifically regarding site works. 
The Clerk of Work Plays a crucial role in Construction Management, ensuring that mechanical ( e.g., HVAC, Plumbing, and Fire Protection Systems) and Electrical (e.g., power distribution, lighting and IT communications wiring) components are specified, Co- Ordinated, and installed according to project specifications.
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

To report to and take instructions from the Design Team and the Project Manager. To liaise as necessary with the Maintenance Manager. The Clerk of Works will have no authority to modify the design, incur additional costs or approve samples.  Moreover, he/she will have no authority to direct the main contactors methods of work or be empowered to issue variations from the contract documents.
To assist in the correct interpretation of all documents and to ensure that all works are carried out in accordance with the drawings, specification and other contract documents.
To advise the Design Team of any additional information required by the contractor.
To check that all workmanship and material meet the standards and performance criteria for the project and to identify and record unacceptable work as soon as possible for the information of the Architect/Design Team accordingly.
Implement Permit-to-Work procedures and co-ordinate with relevant staff the management of interfacing shutdowns, connections and commissioning of services and building works under the contract, reporting to the Architect and the Estates Department as necessary.
To report to the Design team on the implementation of the main contractors programme for the works, preparing progress reports, keeping records of instructions, variations and day works.
To record any factors that could give rise to claims for disruption or affect the projects progress.
To assist the Design Team in site inspections.
To identify and maintain an up to date schedule of remedial items.
To accompany all Local Authority Inspectors on their visits to site, maintaining the necessary liaison with the Local Authorities, as appropriate, in respect of compliance with statutory requirements.
To attend Design Team meetings, both on and off site, and site meetings as required.
To keep a detailed accurate diary of all events pertaining to the job, to include site reports, recording progress, material delivery and site labour and plant. Diary to be prepared in a form to be agreed with the Employers Representative (Architect).
Attend meetings arranged by the Engineering Department as required and furnish such reports as required.
Project Coordination: Work closely with project managers, architects, and engineers to review all design plans, specifications, and drawings.
Conduct in situ / above ceiling surveys to ensure that all new  wiring and containment installations meet design, safety, and quality requirements.
Ensure that M&amp;amp;E systems are designed and installed in accordance with the design documents and that containment can be installed in a coordinated manner with existing systems and building fire compartmentalisation.
Coordinate with subcontractors to ensure the scheduled installation of systems throughout a building campus or standalone buildings.
Witnessing of S/N testing of new  installations.
Compiling Handover and “As built” documentation for the various projects.
Constructability Reviews &amp;amp; Compliance: Review and interpret technical service routing drawings (mechanical, electrical, plumbing) to ensure compliance with the project’s design intent, building codes, and industry standards.
Identify potential conflicts between M&amp;amp;E systems and structure and resolve them before installation.
Ensure compliance with local regulations, codes, and safety standards.
On-site Supervision: Oversee the installation of all systems on-site to ensure quality and adherence to specifications.
Communication &amp;amp; Liaison: Act as the point of contact between the project team, subcontractors, and clients for all -related issues.
Facilitate coordination meetings to ensure that all parties are aligned on design changes, timelines, and expectations.
Problem-solving &amp;amp; Troubleshooting: Proactively identify potential problems with mechanical or electrical systems before they occur.
Troubleshoot issues during the construction phase, ensuring they are resolved quickly to avoid project delays.
Documentation &amp;amp; Reporting: Maintain up-to-date records of designs, specifications, and installation progress.
Prepare reports on project status, key issues, and milestones for the project management team.

 
What you need to apply:

Have attained a reasonable standard of general education commensurate with the role and have a satisfactory knowledge of and experience of duties to be performed and be capable of working on his/her own initiative.
Applicants must have served a recognized apprenticeship in a building or construction craft.
Have five years satisfactory supervisory and practical experience of complex building projects.
Possess the requisite knowledge of construction contract procedures and be capable of writing clear and precise reports, keeping work records, measuring and recording all variations from contracts and reading drawings.
Knowledge of and ability to interpret architects/engineers’ drawings, specifications and technical directions.
Have a high standard of practical experience in building construction.
Have a high degree of proficiency / expertise in Microsoft office.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Energy Retrofit Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-20 10:33:22]]></date><referencenumber><![CDATA[1839]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1839&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Energy Retrofit Manager for a company with projects in Cork/Kerry.
The Chief Assistant Technical Services Officer (CATSO) will provide services as appropriate in the development and execution of major capital projects in acute ancl non-acute settings and to plan and supervise the execution of these projects.
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Manage the delivery of the companies major energy and carbon building retrofit programme.
Manage the existing building retrofit programme.
Manage the project and the resources associated with the programme.
Procure, manage and coordinate the Technical Advisors, Design Teams and Energy Performance Advisors working on the programme.
Procure, Manage and coordinate all construction contracts and contractors associated with the programme.
Deliver this programme in two distinct work streams - firstly, a Pilot Programme consisting of 10 no. locations (nationally) and secondly, a large scale national renovation programme.
Liaise and coordinate with other Project Leads (CATSO) across the regional offices to progress the Pilot Programme and to develop an action a plan for large scale programme.
Liaise with External Agencies such as DoH, DPER, NDFA, and SEAi and with CFO and national Service Division offices.
Liaise with Capital &amp;amp; Estates functions in the development and integration of all  policies, strategies and Implementation Plans such as the Asset and Property Strategy.
Assisting in the development of Decarbonisation Plans for new build and building retrofit programmes.
Managing the preparation of a comprehensive brief for the projects in consultation with services and estates personnel and advisors.
Ensuring that the brief is known and understood, in appropriate detail, by all those who are likely to work in the new facility.
Manage the necessary and appropriate consultation processes, meetings and other activities necessary to satisfactory completion of the project.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Acting as senior administrative officer for the management of the project and helping to resolve quickly such issues as may be for resolution and agreement.
Defining requirements for design services, buildings and equipment.
Advising on the selection of Design Teams, other professional services and Contractors for Capital Projects, arranging and managing the procurement processes.
Arranging for preparation of specifications, drawing and contract documents for Capital Projects.
Obtaining approval to proposals as necessary in accordance with protocols and regulations in a timely manner.
Developing proposals with selected design teams and contractors.
Developing action plans for the timely and efficient completion of contracts. Coordinating the tender and control stages of the project, having close liaison with the design team, site supervisory staff, etc. along with facility / hospital personnel.
Supervising staff and contractors in the implementation of agreed programmes.
Working with service management and nurse planners to ensure that the equipping / commissioning team is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Managing and controlling agreed project timescales and budgets for planning, design, construction and equipping and budgets to agreed quality standards.
Anticipating difficulties and problems, especially those arising from phasing, variations, commissioning and vacating, and ensuring that where necessary these are either resolved directly or brought to the notice of the Estates Manager and Project Board, for decisions on avoidable claims for delays, extras etc.
Managing and controlling expenditure on each assigned project. This is to include presentations to senior management and Project Board as required, of information and current estimates of total costs, running statements of financial commitment and forecasts of expenditure.
Checking design team fees accounts with regards to agreed fees and preparing same for certification by the Estates Manaoer. He / she shall process payments to contractors and design team firms for payment in accordance with constraints set down in contract documents, forms of agreement and statutory provisions.
Advising line management on measures appropriate to enable the orderly phasing out of services in old facilities and the transfer to new facilities of staff and services.
Assisting in the orderly phasing of developments by agreeing appropriate arrangements with line management and to keep line management and senior clinical staff informed of the plans as the developments proceed.
Ensuring appropriate maintenance arrangements are put in place for new buildings. The CATSO will assist and support the development of Energy Efficient Design (EED).
Providing technical input and advice to estates development of National Planning, building regulation and technical guidance documents relevant to the health built environment and energy, sustainability and climate action.
Providing professional technical advice and guidance, most specifically in the area of Energy Performance, Energy Efficient Design (EEO) and Towards Carbon Zero approaches and programmes.
Developing and providing EEO training.
Supporting all National and Regional Offices in the application of an Energy Efficient and Towards Carbon Zero Design approach to all works and projects. The CATSO will plan and supervise the execution of minor capital works.
Identifying minor capital Energy and Decarbonisation priorities as identified in Registers of Opportunities.
Preparing an Energy and Decarbonisation minor capital programme in consultation with service managers for approval.
Developing a comprehensive brief for the project for minor capital works in consultation with local managers and Maintenance Officers/Engineering Officers.
Preparing, or arranging for preparation, of plans and contract documents to detail required.
Arranging for the appointment and management of design teams where required.
Arranging for submission of tenders and recommending tenders for acceptance.
Agreeing programme for project with contractors.
Arranging for the management of the minor capital works.
Ensuring that agreed programme is completed within time and tender sum.
Working closely with and supporting Regional Estates Teams in delivering energy and decarbonisation related capital works.
Co-ordinating and managing all related Energy Performance Contract Programmes.
The CATSO will provide advice on the efficient use of energy and work with services personnel and other estates personnel and advisors on the efficient use of energy in healthcare premises.
Monitoring and reporting on the energy consumption in healthcare premises.
Assessing the energy efficiency standards in premises in accordance with current standards and regulations.
Advising on investment proposals in energy saving projects.
Preparing and implementing agreed investment proposals on energy saving projects. The CATSO will assist and support the development and work of Energy Management Teams by:
Supporting the Estates Manager to coordinate and support the management of Energy Bureau nationally.
Providing support and guidance to Estates Energy Officers.
Supporting the implementation of Energy Awareness Management Teams in agreed locations.
Establishing and embedding energy management best practices into the culture and day-to-day activities of staff and relevant stakeholders within the regions.
Working closely with, and supporting Regional Estates Teams in developing and implementing energy management best practices and works locally.
Embedding the energy agenda as a mainstream element in the delivery of the Estates service to health facilities
Will advise on facilities and environmental matters in conjunction with services personnel and other estates personnel, and advisors as required by:
Assisting as necessary in assessing health and safety of facilities and environmental risks.
Co-operating with Fire and Safety Officers, Services Managers, Health and Safety, Risk Management, Occupational Health and Infection Control Staff in addressing facilities improvements with regard to legislative compliance
Support, promote and actively participate in sustainable energy, water and waste initiatives to create a more sustainable, low carbon and efficient health service.
Supporting the preparation and management of Sustainability Management Programmes.
Supporting the preparation and management of procurement strategies and programmes for works and equipment in the area of Energy and Sustainability. Supporting the preparation and management of procurement strategies and programmes for Utilities and Energy.
Supporting the preparation and management of Critical Infrastructure Resilience management programmes.
Will prepare in consultation with appropriate officers and advisors, programmes for the maintenance of buildings, services, equipment and vehicles.
Defining in accordance with overall guidelines, maintenance requirements of all buildings, services, equipment and vehicles under his / her control, minor capital works and fire precautions schemes and proposing priorities in the allocation of resources available for these schemes.
Preparing budgets for the carrying out of the proposed programmes.
Defining the staff or contract resources necessary to discharge agreed programmes and preparing action plans for carrying out of same.
Assisting in defining requirements for all equipment and buildings, especially in seeking ease of maintenance and operation.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Recommending awards of maintenance contracts to outside contractors where for economical or practical considerations such is considered desirable.
Developing proposals with selected contractors.
Obtaining departmental approval to proposals as necessary.
Developing action plans for the timely and efficient completion of all contracts.
Supervising staff and contractors in the implementation of the agreed programme.
Managing and controlling the agreed budget.
Will ensure that all buildings, services, equipment and vehicles under his I her control are adequately maintained in accordance with the approved maintenance programmes by:
Developing planned maintenance routines for all relevant equipment based on manufacturer's instructions, equipment importance and usage rates.
Incorporating maintenance requirements in supply contracts for new equipment and vehicles where appropriate.
Developing regular inspection and maintenance routines for all buildings, services, equipment and vehicles.
Developing guidelines for the safe operation of all equipment.
Will work with and support the activities of the Property Manager to ensure compliance with Property Transaction Protocols and other relevant property related tasks when assigned such as:
Property management and technical advisory services as deemed appropriate for the management of the healthcare estate property portfolio within the assigned area.
To work with the Property Manager to develop and implement a property management strategy and local property plans in collaboration with other key personnel and advisors.
To work with the Property Manager to ensure property requirements are fully integrated with service provision and staffing levels and ensure all cross care group opportunities for property utilisation are maximised within the companies Property portfolio.
To work with the Property Manager to ensure that all property transactions conform to statutory requirements.
To assess the physical infrastructure of the property portfolio including purpose, state of upkeep, capacity, suitability, space utilisation and security.
Provide information to the Property Manager so as to maintain and keep a property asset register including appropriate records of the legal title to properties.
CATSO will ensure that adequate fire prevention and safety measures. and standards are devised and applied.
Discussing with the local authority Fire Officer in the area in association with the Service Manager and Fire Prevention Officers and other relevant staff, fire precaution and safety measures, and their priorities.
Providing a programme for implementation of agreed measures and arranging for employment and training of sufficient fire prevention officers.
Advising and agreeing annual programmes for fire precautions schemes after consultation with local authority Fire Officers in the area and the Service Managers and Fire Prevention Officers.
Ensure work programmes are implemented in line with the Capital &amp;amp; Estates Infrastructure Decarbonisation Roadmap and the wider Climate Action Strategy.
Provide professional technical advice and guidance, specifically in the area of Energy Performance and Energy Efficient Design (EEO) approaches, to support decarbonisation of the healthcare estate.
Have a good understanding and technical knowledge in relation to sustainable infrastructure and building decarbonisation, along with knowledge of current policy and regulation.
Embed sustainable infrastructure as a mainstream element in the delivery of the Capital &amp;amp; Estates service to healthcare facilities.
Support and actively participate in the organisational response to climate action, promoting a sustainable, low carbon and efficient health service
Co-operate with the Health Services Transformation Programme as required to carry out the duties of the post.
Have a working knowledge of the Health Information and Quality Authority (HIQA) Standards as they apply to the role for example, Standards for Healthcare, National Standards for the Prevention and Control of Healthcare Associated Infections, Hygiene Standards etc. and comply with associated protocols for implementing and maintaining these standards as appropriate to the role.
Have a good knowledge of Health and Safety requirements and ensure that Health and safety Legislation is complied with in all aspects of the delivery of the role
Achievement of targets and plans and completion of agreed programme within allocated budget.
Any other duties as assigned.

 
What you need to apply:

Hold a Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) major academic award in Mechanical Engineering or Electrical Engineering accredited by the relevant Professional Institute being Engineers IrelandHave Membership of the relevant professional association: Engineers Ireland.
Have had at least seven years' satisfactory experience in the design, project management and construction of buildings or in the installation or maintenance of the mechanical, electrical and heating services of such buildings.
A high level of knowledge and experience of the construction of buildings and building services and an understanding of the maintenance requirements.
Have a good understanding and technical knowledge in relation to sustainable infrastructure and building decarbonisation, along with knowledge of current policy and regulation and ability to Provide professional technical advice and guidance to support decarbonisation of the healthcare estate.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Energy Retrofit Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-20 10:33:22]]></date><referencenumber><![CDATA[1839-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1839&amp;Itemid=986]]></url><city><![CDATA[Kerry]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Energy Retrofit Manager for a company with projects in Cork/Kerry.
The Chief Assistant Technical Services Officer (CATSO) will provide services as appropriate in the development and execution of major capital projects in acute ancl non-acute settings and to plan and supervise the execution of these projects.
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Manage the delivery of the companies major energy and carbon building retrofit programme.
Manage the existing building retrofit programme.
Manage the project and the resources associated with the programme.
Procure, manage and coordinate the Technical Advisors, Design Teams and Energy Performance Advisors working on the programme.
Procure, Manage and coordinate all construction contracts and contractors associated with the programme.
Deliver this programme in two distinct work streams - firstly, a Pilot Programme consisting of 10 no. locations (nationally) and secondly, a large scale national renovation programme.
Liaise and coordinate with other Project Leads (CATSO) across the regional offices to progress the Pilot Programme and to develop an action a plan for large scale programme.
Liaise with External Agencies such as DoH, DPER, NDFA, and SEAi and with CFO and national Service Division offices.
Liaise with Capital &amp;amp; Estates functions in the development and integration of all  policies, strategies and Implementation Plans such as the Asset and Property Strategy.
Assisting in the development of Decarbonisation Plans for new build and building retrofit programmes.
Managing the preparation of a comprehensive brief for the projects in consultation with services and estates personnel and advisors.
Ensuring that the brief is known and understood, in appropriate detail, by all those who are likely to work in the new facility.
Manage the necessary and appropriate consultation processes, meetings and other activities necessary to satisfactory completion of the project.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Acting as senior administrative officer for the management of the project and helping to resolve quickly such issues as may be for resolution and agreement.
Defining requirements for design services, buildings and equipment.
Advising on the selection of Design Teams, other professional services and Contractors for Capital Projects, arranging and managing the procurement processes.
Arranging for preparation of specifications, drawing and contract documents for Capital Projects.
Obtaining approval to proposals as necessary in accordance with protocols and regulations in a timely manner.
Developing proposals with selected design teams and contractors.
Developing action plans for the timely and efficient completion of contracts. Coordinating the tender and control stages of the project, having close liaison with the design team, site supervisory staff, etc. along with facility / hospital personnel.
Supervising staff and contractors in the implementation of agreed programmes.
Working with service management and nurse planners to ensure that the equipping / commissioning team is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Managing and controlling agreed project timescales and budgets for planning, design, construction and equipping and budgets to agreed quality standards.
Anticipating difficulties and problems, especially those arising from phasing, variations, commissioning and vacating, and ensuring that where necessary these are either resolved directly or brought to the notice of the Estates Manager and Project Board, for decisions on avoidable claims for delays, extras etc.
Managing and controlling expenditure on each assigned project. This is to include presentations to senior management and Project Board as required, of information and current estimates of total costs, running statements of financial commitment and forecasts of expenditure.
Checking design team fees accounts with regards to agreed fees and preparing same for certification by the Estates Manaoer. He / she shall process payments to contractors and design team firms for payment in accordance with constraints set down in contract documents, forms of agreement and statutory provisions.
Advising line management on measures appropriate to enable the orderly phasing out of services in old facilities and the transfer to new facilities of staff and services.
Assisting in the orderly phasing of developments by agreeing appropriate arrangements with line management and to keep line management and senior clinical staff informed of the plans as the developments proceed.
Ensuring appropriate maintenance arrangements are put in place for new buildings. The CATSO will assist and support the development of Energy Efficient Design (EED).
Providing technical input and advice to estates development of National Planning, building regulation and technical guidance documents relevant to the health built environment and energy, sustainability and climate action.
Providing professional technical advice and guidance, most specifically in the area of Energy Performance, Energy Efficient Design (EEO) and Towards Carbon Zero approaches and programmes.
Developing and providing EEO training.
Supporting all National and Regional Offices in the application of an Energy Efficient and Towards Carbon Zero Design approach to all works and projects. The CATSO will plan and supervise the execution of minor capital works.
Identifying minor capital Energy and Decarbonisation priorities as identified in Registers of Opportunities.
Preparing an Energy and Decarbonisation minor capital programme in consultation with service managers for approval.
Developing a comprehensive brief for the project for minor capital works in consultation with local managers and Maintenance Officers/Engineering Officers.
Preparing, or arranging for preparation, of plans and contract documents to detail required.
Arranging for the appointment and management of design teams where required.
Arranging for submission of tenders and recommending tenders for acceptance.
Agreeing programme for project with contractors.
Arranging for the management of the minor capital works.
Ensuring that agreed programme is completed within time and tender sum.
Working closely with and supporting Regional Estates Teams in delivering energy and decarbonisation related capital works.
Co-ordinating and managing all related Energy Performance Contract Programmes.
The CATSO will provide advice on the efficient use of energy and work with services personnel and other estates personnel and advisors on the efficient use of energy in healthcare premises.
Monitoring and reporting on the energy consumption in healthcare premises.
Assessing the energy efficiency standards in premises in accordance with current standards and regulations.
Advising on investment proposals in energy saving projects.
Preparing and implementing agreed investment proposals on energy saving projects. The CATSO will assist and support the development and work of Energy Management Teams by:
Supporting the Estates Manager to coordinate and support the management of Energy Bureau nationally.
Providing support and guidance to Estates Energy Officers.
Supporting the implementation of Energy Awareness Management Teams in agreed locations.
Establishing and embedding energy management best practices into the culture and day-to-day activities of staff and relevant stakeholders within the regions.
Working closely with, and supporting Regional Estates Teams in developing and implementing energy management best practices and works locally.
Embedding the energy agenda as a mainstream element in the delivery of the Estates service to health facilities
Will advise on facilities and environmental matters in conjunction with services personnel and other estates personnel, and advisors as required by:
Assisting as necessary in assessing health and safety of facilities and environmental risks.
Co-operating with Fire and Safety Officers, Services Managers, Health and Safety, Risk Management, Occupational Health and Infection Control Staff in addressing facilities improvements with regard to legislative compliance
Support, promote and actively participate in sustainable energy, water and waste initiatives to create a more sustainable, low carbon and efficient health service.
Supporting the preparation and management of Sustainability Management Programmes.
Supporting the preparation and management of procurement strategies and programmes for works and equipment in the area of Energy and Sustainability. Supporting the preparation and management of procurement strategies and programmes for Utilities and Energy.
Supporting the preparation and management of Critical Infrastructure Resilience management programmes.
Will prepare in consultation with appropriate officers and advisors, programmes for the maintenance of buildings, services, equipment and vehicles.
Defining in accordance with overall guidelines, maintenance requirements of all buildings, services, equipment and vehicles under his / her control, minor capital works and fire precautions schemes and proposing priorities in the allocation of resources available for these schemes.
Preparing budgets for the carrying out of the proposed programmes.
Defining the staff or contract resources necessary to discharge agreed programmes and preparing action plans for carrying out of same.
Assisting in defining requirements for all equipment and buildings, especially in seeking ease of maintenance and operation.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Recommending awards of maintenance contracts to outside contractors where for economical or practical considerations such is considered desirable.
Developing proposals with selected contractors.
Obtaining departmental approval to proposals as necessary.
Developing action plans for the timely and efficient completion of all contracts.
Supervising staff and contractors in the implementation of the agreed programme.
Managing and controlling the agreed budget.
Will ensure that all buildings, services, equipment and vehicles under his I her control are adequately maintained in accordance with the approved maintenance programmes by:
Developing planned maintenance routines for all relevant equipment based on manufacturer's instructions, equipment importance and usage rates.
Incorporating maintenance requirements in supply contracts for new equipment and vehicles where appropriate.
Developing regular inspection and maintenance routines for all buildings, services, equipment and vehicles.
Developing guidelines for the safe operation of all equipment.
Will work with and support the activities of the Property Manager to ensure compliance with Property Transaction Protocols and other relevant property related tasks when assigned such as:
Property management and technical advisory services as deemed appropriate for the management of the healthcare estate property portfolio within the assigned area.
To work with the Property Manager to develop and implement a property management strategy and local property plans in collaboration with other key personnel and advisors.
To work with the Property Manager to ensure property requirements are fully integrated with service provision and staffing levels and ensure all cross care group opportunities for property utilisation are maximised within the companies Property portfolio.
To work with the Property Manager to ensure that all property transactions conform to statutory requirements.
To assess the physical infrastructure of the property portfolio including purpose, state of upkeep, capacity, suitability, space utilisation and security.
Provide information to the Property Manager so as to maintain and keep a property asset register including appropriate records of the legal title to properties.
CATSO will ensure that adequate fire prevention and safety measures. and standards are devised and applied.
Discussing with the local authority Fire Officer in the area in association with the Service Manager and Fire Prevention Officers and other relevant staff, fire precaution and safety measures, and their priorities.
Providing a programme for implementation of agreed measures and arranging for employment and training of sufficient fire prevention officers.
Advising and agreeing annual programmes for fire precautions schemes after consultation with local authority Fire Officers in the area and the Service Managers and Fire Prevention Officers.
Ensure work programmes are implemented in line with the Capital &amp;amp; Estates Infrastructure Decarbonisation Roadmap and the wider Climate Action Strategy.
Provide professional technical advice and guidance, specifically in the area of Energy Performance and Energy Efficient Design (EEO) approaches, to support decarbonisation of the healthcare estate.
Have a good understanding and technical knowledge in relation to sustainable infrastructure and building decarbonisation, along with knowledge of current policy and regulation.
Embed sustainable infrastructure as a mainstream element in the delivery of the Capital &amp;amp; Estates service to healthcare facilities.
Support and actively participate in the organisational response to climate action, promoting a sustainable, low carbon and efficient health service
Co-operate with the Health Services Transformation Programme as required to carry out the duties of the post.
Have a working knowledge of the Health Information and Quality Authority (HIQA) Standards as they apply to the role for example, Standards for Healthcare, National Standards for the Prevention and Control of Healthcare Associated Infections, Hygiene Standards etc. and comply with associated protocols for implementing and maintaining these standards as appropriate to the role.
Have a good knowledge of Health and Safety requirements and ensure that Health and safety Legislation is complied with in all aspects of the delivery of the role
Achievement of targets and plans and completion of agreed programme within allocated budget.
Any other duties as assigned.

 
What you need to apply:

Hold a Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) major academic award in Mechanical Engineering or Electrical Engineering accredited by the relevant Professional Institute being Engineers IrelandHave Membership of the relevant professional association: Engineers Ireland.
Have had at least seven years' satisfactory experience in the design, project management and construction of buildings or in the installation or maintenance of the mechanical, electrical and heating services of such buildings.
A high level of knowledge and experience of the construction of buildings and building services and an understanding of the maintenance requirements.
Have a good understanding and technical knowledge in relation to sustainable infrastructure and building decarbonisation, along with knowledge of current policy and regulation and ability to Provide professional technical advice and guidance to support decarbonisation of the healthcare estate.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[QA on the Floor - Senior Associate ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-24 15:49:49]]></date><referencenumber><![CDATA[1840]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1840&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking candidates with a Quality on the Floor or Micro background on an initial 12-month contract for our Dublin based client who are a global leader in the field of biotechnology. You will report to the QA Manager, playing a pivotal role in the site's Quality Assurance team. As the Quality point of contact for manufacturing and inspection operations, the PQA Senior Associate will contribute to continuous improvement initiatives by undertaking additional responsibilities beyond routine QA duties.
 
 
 
Why you should apply:

This is an excellent opportunity for someone with a Micobiology background who is interested in trasitioning into a QA position

 
 
What you will be doing:

Ensure adherence to safety standards and SOPs in all activities.
Review and approve production batch records and associated documentation for Qualified Person disposition activities.
Provide real-time quality oversight and support for production unit operations, extending to formulation, vial and syringe Fill Finish activities, including media fills and assessment of aseptic interventions.
Conduct inspections of vials and syringes as part of AQLs, annual reserve inspections, and support complaint investigations.
Offer Quality Assurance support for on-the-floor investigations and deviations.
Review and approve deviations for closure, ensuring compliance with appropriate documentation.
Participate in customer complaint investigations.
Conduct routine Quality Assurance walks on the production floor.
Review and issue logbooks, ensuring compliance with procedures.
Provide training and guidance to staff for effective performance.
Review and approve cGMP records, ensuring compliance with appropriate documentation.
Support continuous improvement and Operational Excellence initiatives.
Undertake other tasks/projects as assigned by the manager.
Role supports 24/7 manufacturing so shift work is required and a shift premium is applicable

 
What you need to apply:

University degree in an Engineering or Science-related discipline
Over 4 years of relevant experience in the pharmaceutical or biotechnology industry or an equivalent combination of experience and educational background.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Quality, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-25 16:43:30]]></date><referencenumber><![CDATA[1841]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1841&amp;Itemid=986]]></url><city><![CDATA[Westmeath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Manager for a leading pharmaceutical company in Athlone.
We are seeking an experienced Project Manager to support the pharmaceutical capital projects. The successful candidate will be responsible for leading project execution, managing schedule delivery, coordinating cross-functional teams, and ensuring the project progresses through commissioning, qualification, and validation activities in line with regulatory requirements.
 
Why you should apply:

You will join an innovative team, working among a diverse group of visionaries, thinkers and doers, working on developing pioneering solutions that lead to shared success.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

A strong background in pharmaceutical manufacturing projects and direct experience managing CQV activities is essential.
Lead project planning, execution, monitoring, and control activities.
Develop and maintain detailed project schedules and recovery plans.
Manage, risks, issues, and change controls.
Coordinate multidisciplinary teams including Engineering, CQV, Operations, Quality, Automation, Process Engineering, and Vendors.
Drive project performance against key milestones and deliverables.
Facilitate project meetings and provide clear status updates to senior leadership.
Identify critical path activities and develop mitigation plans for schedule risks.
Ensure turnover packages are completed and transferred in accordance with project requirements.
Coordinate commissioning and qualification activities to support startup and validation readiness.
Manage vendor relationships and ensure delivery in accordance with contract commitments.
Ensure project execution complies with GMP, regulatory, EHS, and company standards.
Any other duties as assigned

 
What you need to apply:

Bachelor degree in Engineering or related discipline.
5 years of Project Management.
Pharma Commissioning Experience
Strong leadership and planning skills.

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Clerk of Works]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-26 09:37:24]]></date><referencenumber><![CDATA[1842]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1842&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Clerk of Works for a building and refurbishment construction projects in Dublin.
To work as part of a multidisciplinary team to ensure that Construction Projects being delivered are of sufficient quality at handover, along with providing assistance to Engineers specifically regarding site works. 
The Clerk of Work Plays a crucial role in Construction Management, ensuring that mechanical ( e.g., HVAC, Plumbing, and Fire Protection Systems) and Electrical (e.g., power distribution, lighting and IT communications wiring) components are specified, Co- Ordinated, and installed according to project specifications.
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

To report to and take instructions from the Design Team and the Project Manager. To liaise as necessary with the Maintenance Manager. The Clerk of Works will have no authority to modify the design, incur additional costs or approve samples.  Moreover, he/she will have no authority to direct the main contactors methods of work or be empowered to issue variations from the contract documents.
To assist in the correct interpretation of all documents and to ensure that all works are carried out in accordance with the drawings, specification and other contract documents.
To advise the Design Team of any additional information required by the contractor.
To check that all workmanship and material meet the standards and performance criteria for the project and to identify and record unacceptable work as soon as possible for the information of the Architect/Design Team accordingly.
Implement Permit-to-Work procedures and co-ordinate with relevant staff the management of interfacing shutdowns, connections and commissioning of services and building works under the contract, reporting to the Architect and the Estates Department as necessary.
To report to the Design team on the implementation of the main contractors programme for the works, preparing progress reports, keeping records of instructions, variations and day works.
To record any factors that could give rise to claims for disruption or affect the projects progress.
To assist the Design Team in site inspections.
To identify and maintain an up to date schedule of remedial items.
To accompany all Local Authority Inspectors on their visits to site, maintaining the necessary liaison with the Local Authorities, as appropriate, in respect of compliance with statutory requirements.
To attend Design Team meetings, both on and off site, and site meetings as required.
To keep a detailed accurate diary of all events pertaining to the job, to include site reports, recording progress, material delivery and site labour and plant. Diary to be prepared in a form to be agreed with the Employers Representative (Architect).
Attend meetings arranged by the Engineering Department as required and furnish such reports as required.
Project Coordination: Work closely with project managers, architects, and engineers to review all design plans, specifications, and drawings.
Conduct in situ / above ceiling surveys to ensure that all new  wiring and containment installations meet design, safety, and quality requirements.
Ensure that M&amp;amp;E systems are designed and installed in accordance with the design documents and that containment can be installed in a coordinated manner with existing systems and building fire compartmentalisation.
Coordinate with subcontractors to ensure the scheduled installation of systems throughout a building campus or standalone buildings.
Witnessing of S/N testing of new  installations.
Compiling Handover and “As built” documentation for the various projects.
Constructability Reviews &amp;amp; Compliance: Review and interpret technical service routing drawings (mechanical, electrical, plumbing) to ensure compliance with the project’s design intent, building codes, and industry standards.
Identify potential conflicts between M&amp;amp;E systems and structure and resolve them before installation.
Ensure compliance with local regulations, codes, and safety standards.
On-site Supervision: Oversee the installation of all systems on-site to ensure quality and adherence to specifications.
Communication &amp;amp; Liaison: Act as the point of contact between the project team, subcontractors, and clients for all -related issues.
Facilitate coordination meetings to ensure that all parties are aligned on design changes, timelines, and expectations.
Problem-solving &amp;amp; Troubleshooting: Proactively identify potential problems with mechanical or electrical systems before they occur.
Troubleshoot issues during the construction phase, ensuring they are resolved quickly to avoid project delays.
Documentation &amp;amp; Reporting: Maintain up-to-date records of designs, specifications, and installation progress.
Prepare reports on project status, key issues, and milestones for the project management team.

 
What you need to apply:

Have attained a reasonable standard of general education commensurate with the role and have a satisfactory knowledge of and experience of duties to be performed and be capable of working on his/her own initiative.
Applicants must have served a recognized apprenticeship in a building or construction craft.
Have five years satisfactory supervisory and practical experience of complex building projects.
Possess the requisite knowledge of construction contract procedures and be capable of writing clear and precise reports, keeping work records, measuring and recording all variations from contracts and reading drawings.
Knowledge of and ability to interpret architects/engineers’ drawings, specifications and technical directions.
Have a high standard of practical experience in building construction.
Have a high degree of proficiency / expertise in Microsoft office.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Utilities Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-08-31 17:28:44]]></date><referencenumber><![CDATA[1843]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1843&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Utilities Project Engineer for a leading pharmaceutical in South Dublin.
The Utilities Project Engineer reports to the F&amp;amp;E (Facilities &amp;amp; Engineering) Readiness Manager and supports the delivery and operational readiness of utility systems for a new fill-finish facility, from mechanical completion through to handover to the operations team. The role requires at least three days per week on site. Site presence is essential to coordinate with construction, commissioning, system owners, maintenance technicians, stores and vendors; verify equipment and documentation; and resolve execution issues at the point of work.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Execute the assigned project plan activities, identifying risks and dependencies, and providing clear progress updates to the F&amp;amp;E Manager and stakeholders.
Establish CMMS readiness in IBM Maximo, including system locations, hierarchy, equipment and child assets, classifications, engineering work requests and asset-number set-up.
Execute commissioning and operational spare-parts readiness: assess vendor recommendations, develop draft approved spares lists, coordinate Z-number creation, validate budget and storage availability.
Define and implement instrument calibration readiness: obtain and classify instrument lists, complete criticality assessment, define calibration scope and strategy, support CCD (critical control device) set-up, and ensure calibration job plans, datasheets, work orders, initial calibrations and loop checks are complete.
Develop the preventative-maintenance programme by reviewing vendor and site standards, drafting and approving PMs/job plans, establishing maintenance structures and sequencing, and ensuring applicable job hazard analyses are identified, developed and effective.
Coordinate vendor and technician training readiness, including training proposals and agreeing course content.
Determine whether vendor SLAs or maintenance agreements are required and coordinate draft development, review and approval with the vendor and internal stakeholders.
Develop, review and track required equipment SOPs and operational documentation, ensuring deliverables support safe GMP operation and handover.
Be heavily involved in commissioning activities as systems come on line, working alongside the project commissioning team, vendors and operations. Support field walkdowns, issue resolution, documentation review, loop-check and initial-calibration readiness.
Work closely with System Owners, Maintenance Supervisors and Technicians, Capital Project Engineers, Quality, Validation, Stores, Finance and vendors to resolve issues and maintain delivery against key dates.
Manage change controls and support investigations, risk assessments and technical problem-solving in accordance with GMP, EHS and site procedures.
Experience in Clean utilities: WFI, clean steam, purified water, process air and nitrogen.
Other utilities: glycol, non-GMP HVAC, instrument air, service/chilled/potable water, LPHW and process waste.
Controlled-temperature units, including fridges and freezers, and associated qualified and non-qualified control systems.

 
What you need to apply:

Bachelor's degree in engineering or equivalent relevant engineering experience.
Typically three or more years' engineering experience in a GMP manufacturing or pharmaceutical project environment; utilities, greenfield start-up or equipment lifecycle experience is strongly preferred. Strong grounding in biotechnology or pharmaceutical manufacturing, including GMP/GDP, data integrity, EHS, change control, deviation/investigation processes and good documentation practice.
Demonstrable experience of maintenance readiness, asset management, calibration, commissioning support, qualification support or operational handover activities.
Strong, hands-on IBM Maximo experience, including locations, asset hierarchies, classifications, work orders, preventative-maintenance structures, job plans, calibration records and spare-parts data.
Experience with Veeva Vault QualityDocs or equivalent document-management systems is desirable.
Experience of change control (Trackwise), GDP-compliant documentation, technical report writing and cross-functional project delivery.
Strong practical mechanical and troubleshooting capability, with the confidence to work alongside maintenance, commissioning and vendor teams on site in a new facility environment.
Able to manage priorities, communicate clearly at all levels and deliver safely to demanding project timelines.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Construction Project Financial Analyst]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-01 10:36:25]]></date><referencenumber><![CDATA[1844]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1844&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[ Construction Project Financial Analyst
 
Team Horizon is seeking a Construction Project Financial Analyst in Dublin. The purpose of this role is to support the financial governance, cost monitoring and financial reporting functions of the National Maternity Hospital at St Vincent’s University Hospital Programme. This person will assist in analysing financial and project cost data, monitoring programme expenditure and supporting financial planning, forecasting and reporting processes to ensure effective financial oversight and compliance with and the programme governance requirements.
 
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
 
What you will be doing:
Financial Oversight and Cost Monitoring

Track expenditure against approved budgets using the programme's financial/cost management platform.
Report on the Cost Breakdown Structure (CBS) aligned to the programme WBS.
Assist with financial modelling and budget projections.
Support Contracts and Claims with financial plans, earned value, cost-to-complete analysis and cash flow forecasting.
Analyse financial/cost data to support budgets, forecasts and performance monitoring.
Assist with cost control and financial governance to keep delivery within budget.
Work with Contracts and Claims and stakeholders to set cost objectives and monitor spend.
Prepare cost reports, including variance analysis, to support governance decision-making.
Track contractor payments and support related financial analysis and cash flow accuracy.
Support review and monitoring of contractor cost performance.
Support implementation of financial processes for capital/programme expenditure and continuous improvement in reporting and cost control.

Service Delivery and Service Improvement

Support the implementation and management of change.
Identify service inefficiencies and implement improvements in line with legislation and best practice.
Stay aware of internal/external factors and local/national issues affecting service delivery.
Adapt work practices to make policies work and ensure the team understands changes.
Support staff through change processes.

 
 
Standards, Regulations, Policies, Procedures &amp;amp; Legislation

Contribute to policy and procedure development for own area.
Ensure day-to-day compliance with Financial Regulations and policies.
Assess compliance with National/EU legislation and policies.
Maintain accuracy and consistency with current standards.
Keep own and team's knowledge of relevant policies, procedures and practices up to date.
Stay current on relevant regulations Financial Regulations, Health &amp;amp; Safety, Employment law, FOI Acts, etc.).
Pursue continuous professional development.
Identify, assess, manage and monitor risk within own area.

Financial Oversight and Cost Monitoring

Track expenditure against approved budgets via the programme's cost management platform.
Report on the Cost Breakdown Structure (CBS) aligned to the WBS.
Support financial modelling and budget projections.
Assist Contracts and Claims with financial plans, earned value, and cash flow forecasting.
Analyse cost data to support budgets and performance monitoring.
Support cost control and financial governance within budget.
Set cost objectives and monitor spend with stakeholders.
Prepare cost reports and variance analysis for governance decisions.
Track contractor payments and support cash flow accuracy.
Monitor contractor cost performance.
Support financial processes and continuous improvement in cost control.

Service Delivery and Service Improvement

Support implementation and management of change.
Identify and fix service inefficiencies per best practice.
Stay aware of factors affecting service delivery.
Adapt work practices and guide the team through changes.
Support staff through change processes.

Standards, Regulations, Policies, Procedures &amp;amp; Legislation

Contribute to policy and procedure development.
Ensure compliance with Financial Regulations and policies.
Assess compliance with National/EU legislation.
Maintain accuracy and consistency with standards.
Keep own/team knowledge of policies and practices current.
Stay current on relevant regulations and legislation.
Pursue continuous professional development.
Identify, assess and manage risk within own area.

What you need to apply:

Knowledge of GAAP, Financial Regulations and Reporting Standards.
Proficient in Power BI, Excel and financial software/spreadsheets.
Working knowledge of the ACONEX Cost Module.
Experience in financial modelling, cost accounting and project accounting.
High accuracy and strong organisational skills.
Experience with complex data in a large organisation, working independently.
Ability to work within financial governance frameworks.
Commitment to professional development.

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Accountancy/Finance]]></category></job><job><title><![CDATA[QC Sr Associate Data Analytic]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-08 16:24:00]]></date><referencenumber><![CDATA[1847]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1847&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[QC Sr Associate Data Analytic
 Team Horizon is seeking a QC Sr Associate Data Analytic for a client in Dublin. This individual will apply advanced data analytics to extract actionable insights, optimize QC workflows, and drive digital transformation in quality operations.  If you are passionate about Quality Control, laboratory analytics, and data science, and want to drive the next evolution of QC digital optimization, we encourage you to apply!
 Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 What you will be doing:

Work in technical teams in the development, deployment and application of applied analytics, predictive analytics, prescriptive analytics.
Translate complex business processes into production level code.
Work alongside software engineers to translate algorithms into viable products meeting business requirements.
Perform exploratory and targeted data analyses using descriptive statistics and other methods.
Develop, evaluate, and maintain AI/ML and generative AI solutions, including model validation, monitoring, and performance optimization.
Work with data engineers on data quality assessment, data cleansing and data analytics.
Generate reports, annotated code, and other projects artifacts to document, archive, and communicate your work and outcomes.
Perform data verification and scenario testing of developed solutions ensuring business requirements are met.
Explore emerging and alternate technologies to support digital solution advancement.
Support code level troubleshooting activities.
Work with IS teams/resolver groups.
Share and discuss findings with team members practicing SAFe Agile delivery model.
Ensure AI/ML/Digital solution development complies with GxP and other regulatory standards, fostering a strong Quality culture.

What you need to apply:
Minimum Qualifications:

Doctorate, Master's + 2–3 years, Bachelor's + 4–5 years, or Diploma + 10–12 years of experience, in Software Engineering, Data Science, or ML Engineering.

Preferred Qualifications:

Experience with machine learning and generative AI (LLMs, RAG, agentic workflows, prompt engineering, fine-tuning, model evaluation) applied to structured and unstructured data.
Strong programming skills in Python and SQL; experience with cloud platforms (AWS, Azure, GCP) and tools such as Spark and Databricks.
Familiarity with MLOps and AI engineering practices (model versioning, monitoring, deployment pipelines, responsible AI) and software engineering fundamentals (e.g., Git).
Experience with BI/visualization tools (Tableau, Power BI, Spotfire) and automation platforms like Power Automate.
Knowledge of GxP compliance and regulated environments; healthcare, biotech, or life sciences experience a plus.
Proven ability to translate complex business problems into scalable, AI-driven solutions and manage multiple priorities with minimal supervision.
Strong communicator and self-starter, comfortable working independently and across global teams.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[IT/Software]]></category></job><job><title><![CDATA[QC Sr Associate Data Analytic]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-08 16:24:00]]></date><referencenumber><![CDATA[1847-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1847&amp;Itemid=986]]></url><city><![CDATA[Remote]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[QC Sr Associate Data Analytic
 Team Horizon is seeking a QC Sr Associate Data Analytic for a client in Dublin. This individual will apply advanced data analytics to extract actionable insights, optimize QC workflows, and drive digital transformation in quality operations.  If you are passionate about Quality Control, laboratory analytics, and data science, and want to drive the next evolution of QC digital optimization, we encourage you to apply!
 Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 What you will be doing:

Work in technical teams in the development, deployment and application of applied analytics, predictive analytics, prescriptive analytics.
Translate complex business processes into production level code.
Work alongside software engineers to translate algorithms into viable products meeting business requirements.
Perform exploratory and targeted data analyses using descriptive statistics and other methods.
Develop, evaluate, and maintain AI/ML and generative AI solutions, including model validation, monitoring, and performance optimization.
Work with data engineers on data quality assessment, data cleansing and data analytics.
Generate reports, annotated code, and other projects artifacts to document, archive, and communicate your work and outcomes.
Perform data verification and scenario testing of developed solutions ensuring business requirements are met.
Explore emerging and alternate technologies to support digital solution advancement.
Support code level troubleshooting activities.
Work with IS teams/resolver groups.
Share and discuss findings with team members practicing SAFe Agile delivery model.
Ensure AI/ML/Digital solution development complies with GxP and other regulatory standards, fostering a strong Quality culture.

What you need to apply:
Minimum Qualifications:

Doctorate, Master's + 2–3 years, Bachelor's + 4–5 years, or Diploma + 10–12 years of experience, in Software Engineering, Data Science, or ML Engineering.

Preferred Qualifications:

Experience with machine learning and generative AI (LLMs, RAG, agentic workflows, prompt engineering, fine-tuning, model evaluation) applied to structured and unstructured data.
Strong programming skills in Python and SQL; experience with cloud platforms (AWS, Azure, GCP) and tools such as Spark and Databricks.
Familiarity with MLOps and AI engineering practices (model versioning, monitoring, deployment pipelines, responsible AI) and software engineering fundamentals (e.g., Git).
Experience with BI/visualization tools (Tableau, Power BI, Spotfire) and automation platforms like Power Automate.
Knowledge of GxP compliance and regulated environments; healthcare, biotech, or life sciences experience a plus.
Proven ability to translate complex business problems into scalable, AI-driven solutions and manage multiple priorities with minimal supervision.
Strong communicator and self-starter, comfortable working independently and across global teams.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[IT/Software]]></category></job><job><title><![CDATA[Commercial Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-09 12:27:53]]></date><referencenumber><![CDATA[1849]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1849&amp;Itemid=986]]></url><city><![CDATA[Dublin ]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Commercial Manager to Lead commercial performance across major industrial scaffolding projects, driving cost control, contract success and growth while supporting teams, clients and developing your career.
 
Why you should apply:

This role offers a top-tier package, including a strong pension plan, life assurance at four times your salary, generous maternity pay, and an employee assistance programme to support your wellbeing.
You'll also benefit from educational assistance, clear career progression opportunities, Long Service Awards, and a refer-a-friend scheme, this is a package built to reward and support you for the long haul.

 
What you will be doing:

The Commercial Manager has overall responsibility for the commercial management and financial performance of industrial services projects and contracts.
The role ensures robust cost control, contract administration, risk management and commercial governance across multiple projects while supporting profitable growth and protecting the company's commercial interests.
The position acts as a key business partner to operational leadership, clients and senior management, providing commercial insight and strategic support to maximise contract performance and margin delivery, and commercial leadership across the division, ensuring that projects are delivered profitably while supporting operational teams and maintaining strong client relationships.
Key Responsibilities include –
Commercial Management
Contract Administration
Financial Control
Stakeholder Management
Team Leadership
Risk &amp;amp; Governance

 
What you need to apply:

Significant Quantity Surveying experience within industrial services, construction, engineering, utilities or infrastructure sectors. 
Experience managing large-scale contracts and complex commercial arrangements. 
Strong contract administration and commercial negotiation skills. 
Experience leading commercial teams and mentoring developing surveyors. 
Proven track record of improving financial and commercial performance. 
Qualifications and Experience Degree in Quantity Surveying, Construction Economics or related discipline.  Professional accreditation (RICS, SCSI or equivalent) desirable. 
Strong understanding of construction and engineering contracts. 
Full driving licence. 
Commercial acumen &amp;amp; Contract management 
Financial analysis and forecasting 
Negotiation and influencing 
Risk management 
Cost control and budgeting 
Leadership and team development 
]]></description><salary><![CDATA[€85 - €105,000 PA - DOE ]]></salary><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Management]]></category></job><job><title><![CDATA[Operations Director ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-09 12:30:44]]></date><referencenumber><![CDATA[1850]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1850&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking an Operations Director to lead safe, efficient industrial scaffolding operations across multiple sites, inspire strong teams, build trusted client relationships and drive lasting business performance.
 
Why you should apply:

This role offers a top-tier package designed to reward and support you well beyond the day-to-day. Alongside a strong pension plan and life assurance cover worth four times your annual salary, you'll benefit from an employee assistance programme to support your wellbeing, generous maternity pay, and educational assistance to help you keep growing your skills.
The company also invests in your long-term future through clear career progression opportunities and Long Service Awards that recognise loyalty and commitment, while a refer-a-friend scheme means you can be rewarded for helping build the team around you.
It's a package built not just to attract talent, but to look after it for the long haul.

 
What you will be doing:

The Operations Director is responsible for the safe, efficient and profitable delivery of industrial services operations across multiple client sites.
The role provides strategic and operational leadership to field teams, ensuring projects are delivered on time, within budget and in accordance with company, client and regulatory requirements.
The position acts as the key link between senior leadership, clients and operational teams, driving performance, operational excellence, safety culture and continuous improvement across the business.
The successful candidate will be a visible operational leader who combines strong commercial awareness with a relentless focus on safety, people and delivery.
They will build high-performing teams, foster strong client relationships and drive operational excellence across the business.
Key Responsibilities include-
Operational Leadership and Client &amp;amp; Commercial Management
Health, Safety, Environment &amp;amp; Quality
People Leadership
Financial Management
Planning &amp;amp; Performance
Key Performance Indicators

 
What you need to apply:

Significant operational leadership experience within industrial services, scaffolding, construction, engineering, utilities or a related environment. 
Experience managing large operational teams across multiple locations. 
Proven track record of delivering operational and commercial performance. 
Strong client and stakeholder management experience. 
Experience leading safety-focused organisations. 
Budget and P&amp;amp;L responsibility experience. 
Health &amp;amp; Safety qualification. 
Full driving licence.

 
 ]]></description><salary><![CDATA[€100,000 - €130,000 PA - DOE ]]></salary><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Management]]></category></job><job><title><![CDATA[Moulding Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-09 13:45:35]]></date><referencenumber><![CDATA[1851]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1851&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Moulding Engineer for a leading manufacturing company in Sligo.
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Sligo.

 
What you will be doing:

To partner with quality to ensure product attributes and performance achieve all specifications.
To ensure the performance of day to day preventative and demand maintenance activity to maintain manufacturing equipment.
To liaise with Production to ensure equipment performance is maximised.
To maintain records and documentation on relevant Engineering.
Procedures and preventative/ demand maintenance.
To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining trouble shooting, and installing/commissioning equipment.
Technical design making and project planning for new mould tools and processes.
Integration of new Injection Mould tooling and equipment in manufacturing processes.
Technical oversight on existing lines, investigation yields and quality trends.
Prepare appropriate CAPA plans and implement per timelines.
Leading projects against agreed project milestones.
Partnering with Marketing and Business Development, Customers, Suppliers, Vendors and Internal Cross-Functional teams as required.
Ensuring projects are delivered on-time and within budget according to business requirements.
Coordination and analysis of metrology measurements during product development phases.
Decision making on mould design and steel adjustments to meet tight tolerances.
Establish calibration, preventive maintenance and spare parts programmes.
Ensure compliance with calibration and maintenance requirements.
Ensure safety standards are met and safe working practices adhered to.
Ensuring compliance with all Quality, Regulatory, GMP requirements and adherence to all copmpany policies and relevant legislation.
Participate in Risk Management activities as required.
All other duties as requested or assigned.

 
What you need to apply:

A relevant technical qualification in engineering/science/moulding.
Degree Level preferable and or relevant experience.
5-7 years+ relevant experience.
Demonstrated knowledge of molding, extrusion and/or polymer processes and technologies.
Strong analytical problem-solving skills; statistics knowledge/experience would be advantageous.
Previous project/process management, product technology transfer /NPI and validation experience is desirable.
Results driven with proven ability to prioritize work.
Proven ability to deliver projects on time and within budget.
Good working knowledge of quality systems would be helpful.
Excellent written and verbal communication skills is essential.
Working knowledge of AutoCad and/or Solidworks is a benefit.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-09 17:21:33]]></date><referencenumber><![CDATA[1852]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1852&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer for a leading manufacturing company in Sligo.
Will join a team of 6 reporting to Capital Projects Manager, will be supporting a number of small/medium sized capital projects related to equipment/installation/construction. Mechanical/Chemical/Process engineering background.
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Sligo.

 
What you will be doing:

To provide Engineering services to the plant, in order to maximise the availability of all Site Process Equipment and Utilities.
To manage capital engineering projects within site following the Project Lifecycle approach (typical project value range: anything up to €5 million).
To support the engineering teams in controlling uptime of process equipment and optimizing efficiencies both in equipment and process performance.
To support the Engineering team with the emphasis on continual operational improvements.
To provide process engineering support and technical trouble shooting within the site.
To improve the operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives.
To manage the execution of projects within the engineering group including specific Process Safety Projects.
To support the provision of process safety initiatives to the site.
To liaise with Production to ensure equipment performance is maximized.
To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining, troubleshooting and installing/commissioning equipment.
To provide engineering support and technical trouble shooting to all site operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives.
Leadership of process equipment commissioning and validation activities.
Identification and project management of continuous improvement projects.
Work closely with all site functions and other departments to deliver these continuous improvement projects.
Preparation of feasibility studies and budget management for all assigned projects.
Management and negotiation of external contracts and contractors.
Support all major site initiatives and sites core goals.
Any duties as assigned.

 
What you need to apply:

Degree in a relevant Engineering Discipline (Mechanical/Chemical/Process).
5 years + strong site experience in API Manufacturing / OSD Manufacturing / BioPharm but will consider more junior (3 years) if they have relevant project site experience.
Proven track record in delivering Capital Projects – new equipment, utilities, facilities, etc.
Good knowledge of change control and C&amp;amp;Q processes/execution.
API process equipment trains (reactors, filter dryers, pumps, process pipework, milling, containment technology – gloveboxes, downflow booths, etc.).
Drug Product equipment (tablet press, roller compaction, tablet coater, material handling – post hoists, blenders, milling – Quadro Comils, etc.)
Cleanroom processing/utilities – HVAC, CIP systems, Purified water generation and distribution systems, etc.
Knowledgeable/competent with executing change control.
Experience in process engineering, with relevant experience of batch processing, automation, project management, commissioning and validation, equipment reliabilyAPI process equipment trains (reactors, filter dryers, pumps, process pipework, milling, containment technology – gloveboxes, downflow booths, etc.).
Drug Product equipment (tablet press, roller compaction, tablet coater, material handling – post hoists, blenders, milling – Quadro Comils, etc.) Cleanroom processing/utilities – HVAC, CIP systems, Purified water generation and distribution systems, etc.
Knowledgeable/competent with executing change control.
Experience in process engineering, with relevant experience of batch processing, automation, project management, commissioning and validation, equipment reliability and continuous improvement.
Working knowledge of distributed control systems, such as Delta V.
This is a hand-on role requiring a logical and structured approach to resolving day to day engineering issues typical of a live manufacturing environment.
Knowledge of cGMP and regulatory requirements relating to the Healthcare industry is required.
Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements. 
Trackwise change control system experience.
Electrical background – competency with electrical system design &amp;amp; installation (process equipment and site electrical infrastructure), familiar with ATEX regulations and requirements.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Construction Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-15 14:01:31]]></date><referencenumber><![CDATA[1853]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1853&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Construction Project Manager for a company based in Cork city with project in Cork and Kerry.
The Client provides a range of professional, technical, project management, property, fire &amp;amp; safety, and related services in respect of the procurement, development, operation, and maintenance of buildings, plant, and equipment. These services include design, specification, project management, supervision, and procurement associated with building and refurbishment works in the Cork /Kerry region
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Managing the preparation of a comprehensive brief for the projects in consultation with organisational service personnel and advisors.
Ensuring that the project brief is known and understood, in appropriate detail, by all those who are likely to work in the new facility.
Managing the necessary and appropriate consultation processes, meetings and other activities necessary to satisfactory completion of the project.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Acting as senior administrative officer for the management of the project and helping to resolve quickly such issues as may be for resolution and agreement.
Defining requirements for design services, buildings and equipment.
Advising on the selection of Design Teams, other professional services and Contractors for Projects, arranging and managing the procurement processes.
Arranging for preparation of specifications, drawing and contract documents for Projects.
Obtaining approval to proposals as necessary in accordance with organisation protocols and regulations in a timely manner.
Developing proposals with selected design teams and contractors.
Developing action plans for the timely and efficient completion of contracts.  Co-ordinating the tender and control stages of the project, having close liaison with the design team, site supervisory staff, etc. on the one hand and hospital personnel on the other.
Supervising staff and contractors in the implementation of agreed programmes.
Working with service management and ancillary services  to ensure that the equipping/commissioning team  is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Ensuring that the equipping/commissioning team is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Managing and controlling agreed project timescales and budgets for planning, design, construction and equipping and budgets to agreed quality standards.
Anticipating difficulties and problems, especially those arising from phasing, variations, commissioning and vacating, and ensuring that where necessary these are either resolved directly or brought to the notice of the Engineering Manager and Engineering Director , for decisions on avoidable claims for delays, extras etc.
Managing and controlling expenditure on each assigned project. This is to include presentations to senior management and Project Board as required, of information and current estimates of total costs, running statements of financial commitment and forecasts of expenditure.
Checking design team fees accounts with regards to agreed fees and preparing same for certification by the Engineering Manager.  He/she shall process payments to contractors and design team firms for payment in accordance with constraints set down in contract documents, forms of agreement and statutory provisions. o            Advising line management on measures appropriate to enable the orderly phasing out of services in old facilities and the transfer to new facilities of staff and services.  o Assisting in the orderly phasing of developments by agreeing appropriate arrangements with line management and to keep line management and senior clinical staff informed of the plans as the developments proceed.
Ensuring appropriate maintenance arrangements are put in place for new buildings.
Developing a comprehensive brief for the project for minor capital works in consultation with local managers and Maintenance Officers/Engineering Officers.
Preparing or arranging for preparation of plans and contract documents to detail required.
Arranging for the appointment and management of design teams where required.
Arranging for submission of tenders and recommending tenders for acceptance.
Agreeing programme for project with contractors.
Arranging for the management of the minor capital works.
Ensuring that agreed programme is completed within time and tender sum.
Prepare in consultation with appropriate teams, programmes for the maintenance of buildings, services, equipment and vehicles (under his/her control).
Defining in accordance with overall guidelines, maintenance requirements of all buildings, services, equipment and vehicles under his/her control, minor capital works and fire precautions schemes and proposing priorities in the allocation of resources available for these schemes.
Preparing budgets for the carrying out of the proposed programmes.
Defining the staff or contract resources necessary to discharge agreed programmes and preparing action plans for carrying out of same.
Draw up, or in appropriate circumstances, arrange for the development of plans and contract arrangements for the implementation of approved project / maintenance programmes.
Assisting in defining requirements for all equipment and buildings, especially in seeking ease of maintenance and operation.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Recommending awards of maintenance contracts to outside contractors where for economical or practical considerations such is considered desirable.
Developing proposals with selected contractors.
Obtaining departmental approval to proposals as necessary.
Developing action plans for the timely and efficient completion of all contracts.
Supervising staff and contractors in the implementation of the agreed programme.
Managing and controlling the agreed budget.
Ensure that all organisation’s  buildings, services, equipment and vehicles under his/her control are adequately maintained in accordance with the approved maintenance programmes.
Developing planned maintenance routines for all relevant equipment based on manufacturer’s instructions, equipment importance and usage rates.
In-corporating maintenance requirements in supply contracts for new equipment and vehicles where appropriate.
Developing regular inspection and maintenance routines for all buildings, services, equipment and vehicles.
Developing guidelines for the safe operation of all equipment.
Work with and support the activities of the Organizations Property Manager to ensure compliance with Property Transaction Protocols and other relevant property related tasks when assigned.
Property management and technical advisory services as deemed appropriate for the management of the healthcare estate property portfolio within the assigned area.
To work with the Property Manager to develop and implement a property management strategy and local property plans in collaboration with other key personnel and advisors.
To work with the Property Manager to ensure property requirements are fully integrated with service provision and staffing levels and ensure all cross-care group opportunities for property utilisation are maximised within the Organisations Property portfolio.
To work with the Property Manager to ensure that all property transactions conform to statutory requirements.
To assess the physical infrastructure of the Organisations property portfolio including purpose, state of upkeep, capacity, suitability, space utilisation and security.
Provide information to the Property Manager to maintain and keep a property asset register including appropriate records of the legal title to properties.
Discussing with the local authority Fire Officer in the area in association with the Service Manager and Fire Prevention Officers and other relevant staff, fire precaution and safety measures, and their priorities.
Providing a programme for implementation of agreed measures and arranging for employment and training of sufficient fire prevention officers.
Advising and agreeing annual programmes for fire precautions schemes after consultation with local authority Fire Officers in the area and the Service Managers and Fire Prevention Officers.
Provide advice on the efficient use of energy and work with services personnel and other organisational  personnel and advisors on the efficient use of energy in premises.
Monitoring and reporting on the energy consumption in healthcare premises.
Assessing the energy efficiency standards in premises in accordance with current standards and regulations.
Advising on investment proposals in energy saving projects.
Preparing and implementing agreed investment proposals on energy saving projects.
Advise on facilities and environmental matters in conjunction with services personnel and other capital &amp;amp; estates personnel, and advisors as required by:
Assisting as necessary in assessing Health &amp;amp; Safety of facilities and environmental risks.
Co-operating with Fire and Safety Officers, Services Managers, Health &amp;amp; Safety, Risk Management in addressing facilities improvements with regard to legislative compliance.

 
What you need to apply:

Hold a Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) major academic award in Architecture, Engineering or Surveying accredited by the relevant Professional Institute (Society of Chartered Surveyors in Ireland, Royal Institution of Chartered Surveyors, Engineers Ireland, Royal Institute of Architects of Ireland).
Have Full Membership of the relevant professional association1: Society of Chartered Surveyors in Ireland or Royal Institution of Chartered Surveyors or Engineers Ireland or Royal Institute of Architects of Ireland.
Have had at least seven years satisfactory &amp;amp; relevant experience in planning, design, project management or construction of buildings or in the installation or maintenance of the mechanical, electrical, and heating services of such buildings to include ICT Wiring and containment
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Metrology Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-16 09:45:11]]></date><referencenumber><![CDATA[1854]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1854&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Metrology Engineer for a leading pharmaceutical company in Sligo.
To provide a metrology service with an emphasis on continual improvement. The metrology service extends in equal measure to both commercial manufacture and new product introductions. The metrology service is broken into 4 work streams; moulded component batch release, tooling development in support of new product introductions, measurement system development/qualification &amp;amp; calibrations.
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

All work streams are executed in continual compliance with the policies relating to Personnel, Quality, Engineering, Safety and Finance.
To provide analytical support for moulded component batch release as and when required.  
To create and review Metrology reports as required in support of moulded component batch release and engineering study development.
To maintain &amp;amp; troubleshoot measurement systems to ensure their continued optimum performance.
Contentious improvement metrology systems and processes for efficiency and customer satisfaction.
To conduct statistical analysis on measurement results generated from the dimensional inspection of samples from moulding runs for new product introductions and replacement tools.
Generation and maintenance of documentation required in support of new and existing metrology systems and process.
To develop and qualify measurement systems for new product introductions as per project timelines.
Ensure safety standards are met and safe working practices are adhered to.
Implementation of all relevant policies relating to Personnel, Quality, Engineering &amp;amp; Safety.
Identification and implementation of metrology and/or manufacturing related cost improvement projects and initiatives.
Specification, evaluation and selection of new metrology equipment as and when required.
Development of documentation for metrology equipment for compliance with plant systems for calibration and preventive maintenance.
Generation of validation documentation for the Installation Qualification and Operational Qualification of new metrology equipment.
Carrying out component drawing assessments in order to evaluate their suitability for dimensional inspection.
Providing recommendations to design owners on how make component drawings more suitable for dimensional inspection.
Participation in cross functional design for excellence workshops.
Liaise with Division Engineering &amp;amp; R&amp;amp;D as required.
Design and development of prototype fixtures for evaluation through Gauge R&amp;amp;R
Covey learnings from prototypes to fixture manufactures for incorporation into final design.
Participation in fixture design reviews prior to manufacture.
Introducing fixtures per project timelines and budgets.
Generation of the required supporting metrology documentation for equipment, fixtures and Gauge R&amp;amp;R.
Measurement routine development or the overseeing of measurement routine development by external contractors.
Design and qualification of instrument generated measurement reports in compliance with corporate and site data integrity policies and procedures.
Coordination of Gauge R&amp;amp;R activities including statistical analysis and report generation.
Compliance with the Site Priority List.
Present project status updates at various management levels
Overseeing tooling development measurements.
Data analysis including statistical analysis on metrology results.
Troubleshooting and maintenance of metrology equipment, fixtures and measurement routines for quality and efficiency improvement.
Interface with suppliers and plant customers.
Ensure the effective management of appropriate internal and external plant projects.
Development and maintenance of metrology schedules and capacity plans.
Preparation of capital expenditure requests for plant.
Ensure successful external, Division and Corporate audits.
Issue management reports as requested and on time.
Management of relevant budgets within target.
Supervise external contractors.
Negotiate cost / quality effective external contracts.
Prepare appropriate CAPA plans and implement timelines.
Comply with the EHS policy and procedures and demonstrate EHS best practices in all work activities.
Continually be conscious of your own safety and that of others, always complying with safety notices and barriers.
Report any EHS incidents and/or Near Misses (unsafe acts and conditions) immediately to your supervisor and always raise the event in eAchieve;
Support a culture of EHS excellence by recognizing and submitting opportunities for EHS improvement on eAchieve;
Attend all required EHS training and medical surveillance programs;
Wear PPE as required.
Any other duties as assigned.  

 
What you need to apply:

A minimum of an Ordinary Degree (Level 7) in Engineering or related discipline is required.
+2 years’ experience as a Metrology Technician or similar in combination products or a highly regulated industry.
Required to undertake specific investigations, and equipment monitoring, with the view to improve manufacturing performance e.g. reducing equipment downtime and maximizing output and yield.
It may be necessary to re-design elements of manufacturing equipment to adapt to process conditions in order to improve efficiency.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Manager (AI Deployment Manager)]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-18 13:03:51]]></date><referencenumber><![CDATA[1855]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1855&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Manager (AI Deployment Manager) for a our client based in Dublin. We are seeking an AI Deployment Manager (Content Development) to drive the deployment of AI-enabled solutions across Centralized Content projects. The role will focus on improving content creation, content reuse and localisation through the evaluation, design and implementation of AI-enabled tools and workflows.
 
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.

 
 
What you will be doing:

Manage the pilot of generative AI solutions for creating first drafts of strategic story decks, congress updates and other priority content.
Assess suitable tools, define priority use cases and evaluate opportunities to improve the efficiency and quality of content development.
Develop a modular content plan and reusable content architecture for content, claims and approved content blocks.
Define tagging, maintenance and reuse principles to enable faster adaptation of approved content across markets and channels.
Define and test an AI-enabled localisation solution for approved GSL materials following Velocity implementation.
Assess AI-supported translation capabilities and improve the findability of approved source materials, including through ARI.
Collaborate with the Centralized Content team and relevant stakeholders to ensure solutions are practical, scalable and aligned with governance and approval workflows.
Document findings, recommendations and implementation requirements, and communicate progress to key stakeholders.
Identify opportunities to improve content supply chain efficiency through automation, standardisation and responsible use of AI.

 
What you need to apply:

Experience in content operations, content supply chain, digital transformation or AI-enabled workflow implementation. 
Experience evaluating or implementing AI, automation or generative AI solutions. 
Understanding of content modularisation, content reuse and localisation processes. 
Strong project management, analytical and problem-solving skills. 
Ability to work collaboratively with cross-functional and international teams.
Experience in the pharmaceutical, healthcare or life sciences sector would be advantageous.
Knowledge of regulated content, scientific communications and approval workflows would be an advantage.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Commercial]]></category></job><job><title><![CDATA[Project Engineer - Syringe Inspection Equipment]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-21 12:41:09]]></date><referencenumber><![CDATA[1856]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1856&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer (Syringe Inspection) for a client in Dublin who will support the installation, validation, and lifecycle management of automated syringe inspection systems within a GMP fill-finish facility expansion.
 
Why you should apply:
●  This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
●  There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
●  Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.
 
What you will be doing:
●  Act as System Owner (SO) for automated syringe inspection systems.
●  SO during the FAT/SAT, commissioning, qualification, and validation activities.
●  Ensure compliance with GMP, Annex 1, and data integrity requirements.
●  Own system performance metrics including: False reject rates, Detection capability, OEE performance
●  Support inspection recipe development and optimisation.
●  Develop maintenance and lifecycle strategies for inspection equipment.
●  Lead troubleshooting and root cause investigations for inspection failures.
●  Support audit readiness and regulatory inspections.
 
What you need to apply:
●  Bachelor’s Degree in Engineering (Mechanical, Electrical, Automation, or related discipline).
●  5+ years’ experience in biopharmaceutical manufacturing.
●  Experience with Automated visual inspection systems (AVI), Vision systems, High-speed packaging or inspection lines
●  Understanding of particulate detection, cosmetic defect inspection, and container closure integrity.
●  Experience supporting equipment validation and data integrity compliance.
●  Strong analytical and problem-solving skills.]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Operational Excellence Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-21 16:32:57]]></date><referencenumber><![CDATA[1857]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1857&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[ 
Team Horizon is seeking an Operational Excellence Specialist for our Clients manufacturing facility in Dublin on an initial 12-month contract.
 
 
Why you should apply:

You will have the opportunity to lead initiatives that enhance our operational capabilities, ensuring we meet our strategic ambitions and continue to transform the lives of patients globally.
Hybrid Role

 
What you will be doing:

Lead supply chain efficiency initiatives to optimise resource allocation and minimise waste.
Embed continuous improvement and Lean methodologies, equipping teams with the tools and knowledge to improve performance.
Develop and adapt standardised work processes to ensure consistency and quality, and facilitate problem-solving workshops.
Conduct value stream mapping to identify bottlenecks and inefficiencies, and implement improvements to workflows and product delivery.
Support the deployment of Design for Lean and Six Sigma methodologies to improve product and process quality.
Develop performance metrics and use data-driven insights to inform strategic decisions and improvements.
Oversee digital transformation projects, integrating digital solutions to streamline processes and improve decision-making.
Support the implementation of global strategies and align improvement initiatives with organisational objectives.
Improve meeting effectiveness, communication and collaboration across teams.
Conduct organisational maturity assessments and develop action plans to address capability gaps.
Lead and support strategic improvement initiatives through training, coaching and stakeholder engagement.
Develop and refine business governance processes to improve operational efficiency and performance management.
Mentor and coach programme sponsors, managers and key users to support effective strategy execution.
Support workplace culture and employee engagement initiatives aligned with organisational values.
Collaborate with central operational excellence teams to adapt standards across operations and build strong stakeholder relationships.
Support recognition initiatives that acknowledge successful project outcomes and employee contributions.
Lead learning and development programmes to build employee skills and knowledge.
Oversee onboarding programmes that integrate new employees into the organisation’s culture and operations

 
What you need to apply:

Bachelor’s degree in science, engineering, business, or a related field is required. 
Desirable certifications include Lean Six Sigma (Black Belt preferred), PMP, Change Management, or Strategic Management, demonstrating a commitment to operational excellence.
Power BI skills
3 years of experience in delivering strategy and business excellence systems, or a similar role within a complex, matrixed organization (preferably in a GxP environment)
Proven decision-making ability and strong communication skills.
Capable of influencing cross-functionally and working collaboratively across diverse teams.
Strong analytical and problem-solving skills, demonstrating a results-oriented mindset.

 
 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[QA Operations Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-22 15:34:22]]></date><referencenumber><![CDATA[1858]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1858&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a QA Operations Manager who will lead the day-to-day Quality Assurance oversight of GMP manufacturing operations to ensure products are manufactured, tested, packaged, stored, and released in compliance with regulatory requirements, company standards, and the site Pharmaceutical Quality System.
 
Why you should apply:

Opportunity to provide quality leadership across manufacturing, packaging, warehouse, engineering, validation, QC, and support functions.
You will ensure effective QA presence on the shop floor, timely review of GMP documentation, robust deviation and batch record management, and proactive identification and escalation of quality risks.

 
What you will be doing:

Actively participate in daily quality operations, ensuring real-time support for Manufacturing, QC, and Compliance systems teams.
Develop, and retain talent in QA, ensuring the team possesses the right GMP expertise, problem-solving skills, and risk-based decision-making capabilities.
Provide coaching, training, and mentorship to embed a culture of proactive quality ownership.
Decision Making/Problem Solving - Identify and understand issues, problems and opportunities and compare data from different sources to draw conclusions and develop solutions consistent with the facts. Natural influencer and ability to form strong relationships cross functionally.
Support regulatory audits and inspections.
Lead or support quality risk assessments related to manufacturing operations, process deviations, contamination control, facility controls, cleaning, equipment, materials, and supply continuity.
Support operational readiness for new products, process changes, facility upgrades, and manufacturing campaigns.
Oversee deviation management, approve CAPAs, and drive continuous improvement. Maintain a strong QA presence on the manufacturing floor to support real-time decision-making and quality risk escalation.
Ensure appropriate quality oversight of critical process steps, line clearances, material movements, hold times, sampling, cleaning, and environmental controls.
Write, review, and revise Standard Operating Procedures (SOPs).
Identify and correct weaknesses, procedural gaps, and policy exceptions to optimize quality control and assurance.
Provide training to employees on quality procedures and compliance.
Collaborate with vendors, contractors, and suppliers to ensure they meet the organization's quality standards.
Support departmental objectives and strategic initiatives.
Other duties as assigned

 
What you need to apply:

Minimum 6 – 8 years of relevant experience in biotech or pharmaceutical industry
Minimum 2-3 years’ experience managing GMP Quality operations activities.
Prior experience interfacing with and managing inspections performed by regulatory bodies. Advanced degree in Biological /Pharmaceutical science discipline.
Experience leading deviation investigations, CAPA, change control, batch record review, and inspection readiness activities.
Experience in leadership roles within a GMP-regulated biologics, vaccines, or sterile manufacturing environment.
Demonstrated success in quality management leadership and the resolution significant quality /technical challenges.
Expertise in EU GMP, regulatory inspections, risk-based QA strategies, and digital transformation in quality systems.
Proven ability to lead teams, optimize QA processes, and drive a culture of continuous improvement.
Strong working knowledge of Industry Compendia, regulations, and standards including USP / Ph. Eur, GMP, EMA, and ICH Specialized Knowledge or Skills
Proficient in quality principles in a manufacturing facility
Must be able to work under pressure and meet deadlines, while maintaining a positive attitude.
Have good communication skills and able to work in collaboration.
Effective time management; deliver results on time.
Excellent computer proficiency (MS Office – Word, Excel, Power Point and Outlook).
Has the ability to read, write and communicate in English.
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management]]></category></job><job><title><![CDATA[Quality Systems Manager ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-22 15:35:28]]></date><referencenumber><![CDATA[1859]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1859&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Quality Systems Manager who can lead the effective management, maintenance, and continuous improvement of the site's Pharmaceutical Quality System (PQS) to ensure compliance with GMP, regulatory requirements, and company standards.
 
 
Why you should apply:

This role provides leadership and oversight of key quality systems including deviations, CAPA, change control, complaints, quality risk management, document control, training, audit management, and management review processes

 
What you will be doing:

Supports and facilitates audits and regulatory inspections.
Develops, improves, and monitors Quality Systems for the organization.
Continuously improves areas impacted by deviations and approves appropriate CAPAs.
Monitor system performance through KPIs and Quality Metrics.
Drive continuous improvement initiatives across all quality systems.
Write and revise standard operating procedures (SOPs).
Provides direction and oversight during active processes and applies understanding of European Union (EU) Veterinary Medicinal Products regulations related to Veterinary Medicinal Products and Continuous improvement.
Decision Making/Problem Solving - Identify and understand issues, problems and opportunities and compare data from different sources to draw conclusions and develop solutions consistent with the facts. Natural influencer and ability to form strong relationships cross functionally.
Correct weaknesses, ineffective procedures, and discrepancies and performs or approves appropriate corrective actions
Write, review, and revise Standard Operating Procedures (SOPs)
Provides Training to new employees.
Able to work effectively with team members and other professionals such as vendors, contractors, or suppliers with the aim of ensuring their products or services meet the organization’s quality standards
Support departmental objectives and strategic initiatives.
Proficiency with Microsoft applications, including Word and Excel and environmental systems.
Other duties as assigned

 
What you need to apply:

Minimum 6 – 8 years of relevant experience in biotech or pharmaceutical industry
Minimum 2 to 3 years’ experience managing GMP Quality Systems.
Prior experience interfacing with and managing inspections performed by regulatory bodies.
Advanced degree in Biological /Pharmaceutical science discipline. 
Demonstrated success in quality management leadership and the resolution significant quality /technical challenges.
Expertise in EU GMP, regulatory inspections, risk-based QA strategies, and digital transformation in quality systems. 
Proven ability to lead teams, optimize QA processes, and drive a culture of continuous improvement.
Strong working knowledge of Industry Compendia, regulations, and standards including USP / Ph. Eur, GMP, EMA, and ICICH Specialized knowledge or Skills 
Proficient in quality principles in a manufacturing facility with a strong quality mindset and proactive approach.
Must be able to work under pressure and meet deadlines, while maintaining a positive attitude. • Have good communication skills and able to collaborate effectively.
Effective time management; deliver results on time.
 Excellent computer proficiency (MS Office – Word, Excel, Power Point and Outlook).
Has the ability to read, write and communicate in English.

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Quality, Management]]></category></job><job><title><![CDATA[Project Engineer - Robotics &amp; AI]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-23 16:27:27]]></date><referencenumber><![CDATA[1860]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1860&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer - Robotics New build for a leading pharmaceutical company in Ireland.
This role combines project engineering and project management with system-level technical leadership in robotics.
The successful candidate will partner with site and global stakeholders to identify and assess robotics opportunities, define requirements and business cases, evaluate solution options and feasibility, and lead projects from concept through successful execution.
The role serves as the technical owner for robotics applications - understanding technology capabilities, limitations, risks, and tradeoffs; challenging vendor recommendations; and guiding solution direction - while external system integrators perform the detailed design, programming, and system build.
Can be a remote role but will be providing global project support which will include 25% travel required.
 
Why you should apply:

You will join an innovative team, working among a diverse group of visionaries, thinkers and doers, working on developing pioneering solutions that lead to shared success.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Co-lead the execution of robotics projects across global sites and new-build programs, including locations where facilities, operating models, and site teams are still being established; coordinate scope, schedule, budget, risks, stakeholders, and external system integrators from concept through implementation.
Collaborate with global, site, and cross-functional new-build teams to define operational needs, project scope, user requirements, success criteria, and deliverables, often while facility designs, processes, and ownership models are still evolving.
Build alignment across global functions, new-build teams, future site stakeholders, and vendors; navigate complex governance and decision processes, resolve ownership gaps and roadblocks, and maintain robotics project momentum while balancing competing priorities and accelerated site-delivery timelines.
Drive timely input and alignment from global and cross-functional stakeholders to define, quantify, and articulate the business value of robotics opportunities, including productivity, capacity, efficiency, safety, and, where relevant, compliance benefits, despite evolving assumptions and competing priorities.
Lead the selection and management of system integrators, equipment suppliers, and technology partners; review proposals, concepts, schedules, risk assessments, and implementation plans; and hold vendors accountable for meeting project requirements.
Provide system-level technical leadership by assessing robotics applications, evaluating technology capabilities and limitations, comparing solution alternatives, and determining feasibility, risks, and scalability. Review and challenge integrator recommendations while relying on external partners for detailed design, programming, and system build.
Support the global robotics team in building the long-term project pipeline by working with site stakeholders to identify and assess future robotics opportunities.
Regularly gather input and feedback from each site to guide the organization’s robotics and automation strategy, addressing both operational value and compliance readiness where necessary.
Lead and oversee small-scale proof-of-concept projects by defining objectives and evaluation criteria, coordinating external partners, assessing results, and recommending whether solutions should be advanced, modified, or discontinued.
Travel internationally as needed and adapt to diverse regulatory requirements, operating cultures, project stages, and new-build environments.
Any other duties as assigned.

 
What you need to apply:

Experience working in regulated industries (such as Pharma, biotechnology, or medical devices) is an advantage, particularly familiarity with Good Manufacturing Practice (GMP), ISO, or FDA requirements, and validation processes (IQ/OQ/PQ). Competence in handling project documentation, risk assessments, and compliance documentation when required.
Proven track record of leading robotics or automation projects in manufacturing, logistics, or laboratory environments, including translating operational needs into requirements, managing external delivery partners, and guiding solutions through implementation and startup. Strong communication, stakeholder management, and influencing skills, with the ability to create alignment across global technical and non-technical teams, clarify ownership, obtain timely decisions, and progress work without direct authority or a fully established site organization.
Adaptive and open mindset, comfortable working in multicultural and multidisciplinary teams, and in both regulated and unregulated pharmaceutical environments.
Background in industrial robotics sales or applications engineering.
Communication and Relationship Development.
Project management and organizational skills to manage multiple projects.
An engineering degree would be good to have but not a must if the candidate has relevant experience. (mechanical, industrial, robotics, electrical, mechatronics).
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Engineer - Robotics &amp; AI]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-23 16:27:27]]></date><referencenumber><![CDATA[1860-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1860&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer - Robotics New build for a leading pharmaceutical company in Ireland.
This role combines project engineering and project management with system-level technical leadership in robotics.
The successful candidate will partner with site and global stakeholders to identify and assess robotics opportunities, define requirements and business cases, evaluate solution options and feasibility, and lead projects from concept through successful execution.
The role serves as the technical owner for robotics applications - understanding technology capabilities, limitations, risks, and tradeoffs; challenging vendor recommendations; and guiding solution direction - while external system integrators perform the detailed design, programming, and system build.
Can be a remote role but will be providing global project support which will include 25% travel required.
 
Why you should apply:

You will join an innovative team, working among a diverse group of visionaries, thinkers and doers, working on developing pioneering solutions that lead to shared success.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Co-lead the execution of robotics projects across global sites and new-build programs, including locations where facilities, operating models, and site teams are still being established; coordinate scope, schedule, budget, risks, stakeholders, and external system integrators from concept through implementation.
Collaborate with global, site, and cross-functional new-build teams to define operational needs, project scope, user requirements, success criteria, and deliverables, often while facility designs, processes, and ownership models are still evolving.
Build alignment across global functions, new-build teams, future site stakeholders, and vendors; navigate complex governance and decision processes, resolve ownership gaps and roadblocks, and maintain robotics project momentum while balancing competing priorities and accelerated site-delivery timelines.
Drive timely input and alignment from global and cross-functional stakeholders to define, quantify, and articulate the business value of robotics opportunities, including productivity, capacity, efficiency, safety, and, where relevant, compliance benefits, despite evolving assumptions and competing priorities.
Lead the selection and management of system integrators, equipment suppliers, and technology partners; review proposals, concepts, schedules, risk assessments, and implementation plans; and hold vendors accountable for meeting project requirements.
Provide system-level technical leadership by assessing robotics applications, evaluating technology capabilities and limitations, comparing solution alternatives, and determining feasibility, risks, and scalability. Review and challenge integrator recommendations while relying on external partners for detailed design, programming, and system build.
Support the global robotics team in building the long-term project pipeline by working with site stakeholders to identify and assess future robotics opportunities.
Regularly gather input and feedback from each site to guide the organization’s robotics and automation strategy, addressing both operational value and compliance readiness where necessary.
Lead and oversee small-scale proof-of-concept projects by defining objectives and evaluation criteria, coordinating external partners, assessing results, and recommending whether solutions should be advanced, modified, or discontinued.
Travel internationally as needed and adapt to diverse regulatory requirements, operating cultures, project stages, and new-build environments.
Any other duties as assigned.

 
What you need to apply:

Experience working in regulated industries (such as Pharma, biotechnology, or medical devices) is an advantage, particularly familiarity with Good Manufacturing Practice (GMP), ISO, or FDA requirements, and validation processes (IQ/OQ/PQ). Competence in handling project documentation, risk assessments, and compliance documentation when required.
Proven track record of leading robotics or automation projects in manufacturing, logistics, or laboratory environments, including translating operational needs into requirements, managing external delivery partners, and guiding solutions through implementation and startup. Strong communication, stakeholder management, and influencing skills, with the ability to create alignment across global technical and non-technical teams, clarify ownership, obtain timely decisions, and progress work without direct authority or a fully established site organization.
Adaptive and open mindset, comfortable working in multicultural and multidisciplinary teams, and in both regulated and unregulated pharmaceutical environments.
Background in industrial robotics sales or applications engineering.
Communication and Relationship Development.
Project management and organizational skills to manage multiple projects.
An engineering degree would be good to have but not a must if the candidate has relevant experience. (mechanical, industrial, robotics, electrical, mechatronics).
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Engineer - Robotics &amp; AI]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-23 16:27:27]]></date><referencenumber><![CDATA[1860-3]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1860&amp;Itemid=986]]></url><city><![CDATA[Remote]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer - Robotics New build for a leading pharmaceutical company in Ireland.
This role combines project engineering and project management with system-level technical leadership in robotics.
The successful candidate will partner with site and global stakeholders to identify and assess robotics opportunities, define requirements and business cases, evaluate solution options and feasibility, and lead projects from concept through successful execution.
The role serves as the technical owner for robotics applications - understanding technology capabilities, limitations, risks, and tradeoffs; challenging vendor recommendations; and guiding solution direction - while external system integrators perform the detailed design, programming, and system build.
Can be a remote role but will be providing global project support which will include 25% travel required.
 
Why you should apply:

You will join an innovative team, working among a diverse group of visionaries, thinkers and doers, working on developing pioneering solutions that lead to shared success.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Co-lead the execution of robotics projects across global sites and new-build programs, including locations where facilities, operating models, and site teams are still being established; coordinate scope, schedule, budget, risks, stakeholders, and external system integrators from concept through implementation.
Collaborate with global, site, and cross-functional new-build teams to define operational needs, project scope, user requirements, success criteria, and deliverables, often while facility designs, processes, and ownership models are still evolving.
Build alignment across global functions, new-build teams, future site stakeholders, and vendors; navigate complex governance and decision processes, resolve ownership gaps and roadblocks, and maintain robotics project momentum while balancing competing priorities and accelerated site-delivery timelines.
Drive timely input and alignment from global and cross-functional stakeholders to define, quantify, and articulate the business value of robotics opportunities, including productivity, capacity, efficiency, safety, and, where relevant, compliance benefits, despite evolving assumptions and competing priorities.
Lead the selection and management of system integrators, equipment suppliers, and technology partners; review proposals, concepts, schedules, risk assessments, and implementation plans; and hold vendors accountable for meeting project requirements.
Provide system-level technical leadership by assessing robotics applications, evaluating technology capabilities and limitations, comparing solution alternatives, and determining feasibility, risks, and scalability. Review and challenge integrator recommendations while relying on external partners for detailed design, programming, and system build.
Support the global robotics team in building the long-term project pipeline by working with site stakeholders to identify and assess future robotics opportunities.
Regularly gather input and feedback from each site to guide the organization’s robotics and automation strategy, addressing both operational value and compliance readiness where necessary.
Lead and oversee small-scale proof-of-concept projects by defining objectives and evaluation criteria, coordinating external partners, assessing results, and recommending whether solutions should be advanced, modified, or discontinued.
Travel internationally as needed and adapt to diverse regulatory requirements, operating cultures, project stages, and new-build environments.
Any other duties as assigned.

 
What you need to apply:

Experience working in regulated industries (such as Pharma, biotechnology, or medical devices) is an advantage, particularly familiarity with Good Manufacturing Practice (GMP), ISO, or FDA requirements, and validation processes (IQ/OQ/PQ). Competence in handling project documentation, risk assessments, and compliance documentation when required.
Proven track record of leading robotics or automation projects in manufacturing, logistics, or laboratory environments, including translating operational needs into requirements, managing external delivery partners, and guiding solutions through implementation and startup. Strong communication, stakeholder management, and influencing skills, with the ability to create alignment across global technical and non-technical teams, clarify ownership, obtain timely decisions, and progress work without direct authority or a fully established site organization.
Adaptive and open mindset, comfortable working in multicultural and multidisciplinary teams, and in both regulated and unregulated pharmaceutical environments.
Background in industrial robotics sales or applications engineering.
Communication and Relationship Development.
Project management and organizational skills to manage multiple projects.
An engineering degree would be good to have but not a must if the candidate has relevant experience. (mechanical, industrial, robotics, electrical, mechatronics).
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Project Manager - Construction]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-25 12:31:46]]></date><referencenumber><![CDATA[1861]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1861&amp;Itemid=986]]></url><city><![CDATA[Kerry]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Project Manager for a company with projects across Kerry and Cork.
The Client provides a range of professional, technical, project management, property, fire &amp;amp; safety, and related services in respect of the procurement, development, operation, and maintenance of buildings, plant, and equipment. These services include design, specification, project management, supervision, and procurement associated with building and refurbishment works in the Cork /Kerry region.
 
Why you should apply:

You will join an innovative team, working among a diverse group of visionaries, thinkers and doers, working on developing pioneering solutions that lead to shared success.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Managing the preparation of a comprehensive brief for the projects in consultation with organisational service personnel and advisors.
Ensuring that the project brief is known and understood, in appropriate detail, by all those who are likely to work in the new facility.
Managing the necessary and appropriate consultation processes, meetings and other activities necessary to satisfactory completion of the project.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Acting as senior administrative officer for the management of the project and helping to resolve quickly such issues as may be for resolution and agreement.
Defining requirements for design services, buildings and equipment.
Advising on the selection of Design Teams, other professional services and Contractors for Projects, arranging and managing the procurement processes.
Arranging for preparation of specifications, drawing and contract documents for Projects.
Obtaining approval to proposals as necessary in accordance with organisation protocols and regulations in a timely manner.
Developing proposals with selected design teams and contractors.
Developing action plans for the timely and efficient completion of contracts. Co-ordinating the tender and control stages of the project, having close liaison with the design team, site supervisory staff, etc. on the one hand and personnel on the other.
Supervising staff and contractors in the implementation of agreed programmes.
Working with service management and ancillary services to ensure that the equipping/commissioning team is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Ensuring that the equipping/commissioning team is established in good time, is adequately briefed and trained, and is effectively supported in carrying out its work.
Managing and controlling agreed project timescales and budgets for planning, design, construction and equipping and budgets to agreed quality standards.
Anticipating difficulties and problems, especially those arising from phasing, variations, commissioning and vacating, and ensuring that where necessary these are either resolved directly or brought to the notice of the Engineering Manager and Engineering Director , for decisions on avoidable claims for delays, extras etc.
Managing and controlling expenditure on each assigned project. This is to include presentations to senior management and Project Board as required, of information and current estimates of total costs, running statements of financial commitment and forecasts of expenditure.
Checking design team fees accounts with regards to agreed fees and preparing same for certification by the Engineering Manager. He/she shall process payments to contractors and design team firms for payment in accordance with constraints set down in contract documents, forms of agreement and statutory provisions.
Advising line management on measures appropriate to enable the orderly phasing out of services in old facilities and the transfer to new facilities of staff and services.
Assisting in the orderly phasing of developments by agreeing appropriate arrangements with line management and to keep line management and senior clinical staff informed of the plans as the developments proceed.
Ensuring appropriate maintenance arrangements are put in place for new buildings.
Plan and supervise the execution of Project works by:
Developing a comprehensive brief for the project for minor capital works in consultation with local managers and Maintenance Officers/Engineering Officers.
Preparing or arranging for preparation of plans and contract documents to detail required.
Arranging for the appointment and management of design teams where required.
Arranging for submission of tenders and recommending tenders for acceptance.
Agreeing programme for project with contractors.
Arranging for the management of the minor capital works.
Ensuring that agreed programme is completed within time and tender sum.
Prepare in consultation with appropriate teams, programmes for the maintenance of buildings, services, equipment and vehicles (under his/her control) by:
Defining in accordance with overall guidelines, maintenance requirements of all buildings, services, equipment and vehicles under his/her control, minor capital works and fire precautions schemes and proposing priorities in the allocation of resources available for these schemes.
Preparing budgets for the carrying out of the proposed programmes.
Defining the staff or contract resources necessary to discharge agreed programmes and preparing action plans for carrying out of same.
Draw up, or in appropriate circumstances, arrange for the development of plans and contract arrangements for the implementation of approved project / maintenance programmes by:
Assisting in defining requirements for all equipment and buildings, especially in seeking ease of maintenance and operation.
Complying with all regulatory requirements including permission, licences, certificates and approvals.
Recommending awards of maintenance contracts to outside contractors where for economical or practical considerations such is considered desirable.
Developing proposals with selected contractors.
Obtaining departmental approval to proposals as necessary.
Developing action plans for the timely and efficient completion of all contracts.
Supervising staff and contractors in the implementation of the agreed programme.
Managing and controlling the agreed budget.
Ensure that all organisation’s buildings, services, equipment and vehicles under his/her control are adequately maintained in accordance with the approved maintenance programmes by:
Developing planned maintenance routines for all relevant equipment based on manufacturer’s instructions, equipment importance and usage rates.
In-corporating maintenance requirements in supply contracts for new equipment and vehicles where appropriate.
Developing regular inspection and maintenance routines for all buildings, services, equipment and vehicles.
Developing guidelines for the safe operation of all equipment.
Work with and support the activities of the Organizations Property Manager to ensure compliance with Property Transaction Protocols and other relevant property related task.s
Property management and technical advisory services as deemed appropriate for the management of the healthcare estate property portfolio within the assigned area.
To work with the Property Manager to develop and implement a property management strategy and local property plans in collaboration with other key personnel and advisors.
To work with the Property Manager to ensure property requirements are fully integrated with service provision and staffing levels and ensure all cross-care group opportunities for property utilisation are maximised within the Organisations Property portfolio.
To work with the Property Manager to ensure that all property transactions conform to statutory requirements.
To assess the physical infrastructure of the Organisations property portfolio including purpose, state of upkeep, capacity, suitability, space utilisation and security.
Provide information to the Property Manager to maintain and keep a property asset register including appropriate records of the legal title to properties.
Ensure that adequate fire prevention and safety measures and standards are devised and applied by:
Discussing with the local authority Fire Officer in the area in association with the Service Manager and Fire Prevention Officers and other relevant staff, fire precaution and safety measures, and their priorities.
Providing a programme for implementation of agreed measures and arranging for employment and training of sufficient fire prevention officers.
Advising and agreeing annual programmes for fire precautions schemes after consultation with local authority Fire Officers in the area and the Service Managers and Fire Prevention Officers.
Provide advice on the efficient use of energy and work with services personnel and other organisational personnel and advisors on the efficient use of energy in premises by;
Monitoring and reporting on the energy consumption in healthcare premises.
Assessing the energy efficiency standards in premises in accordance with current standards and regulations.
Advising on investment proposals in energy saving projects.
Preparing and implementing agreed investment proposals on energy saving projects.
Advise on facilities and environmental matters in conjunction with services personnel and other capital &amp;amp; estates personnel, and advisors as required by:
Assisting as necessary in assessing Health &amp;amp; Safety of facilities and environmental risks.
Co-operating with Fire and Safety Officers, Services Managers, Health &amp;amp; Safety, Risk Management in addressing facilities improvements with regard to legislative compliance.
Any other duties as assigned.

 
What you need to apply:

Hold a Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) major academic award in Architecture, Engineering or Surveying accredited by the relevant Professional Institute (Society of Chartered Surveyors in Ireland, Royal Institution of Chartered Surveyors, Engineers Ireland, Royal Institute of Architects of Ireland).
Or Have Full Membership of the relevant professional association1: - Society of Chartered Surveyors in Ireland - Royal Institution of Chartered Surveyors - Engineers Ireland - Royal Institute of Architects of Ireland Or
Have had at least seven years satisfactory &amp;amp; relevant experience in planning, design, project management or construction of buildings or in the installation or maintenance of the mechanical, electrical, and heating services of such buildings to include ICT Wiring and containment.
Candidates must possess the requisite knowledge and ability (including a high standard of suitability and of administrative capacity) for the proper discharge of the duties of the position.
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Utilities Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-09-25 12:47:12]]></date><referencenumber><![CDATA[1862]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1862&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Utilities Project Engineer for a leading pharmaceutical company in south Dublin.
The Plant Utilities Project Engineer is a site-based role to provide client-side focused technical ownership and field engineering support for the plant utility systems during construction, installation, startup, commissioning and operational readiness.
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

The engineer will take technical ownership of assigned plant utility systems from construction phase through Mechanical Completion, startup, commissioning, operational readiness and final transfer to Site operations.
The principal systems include: Air compressors, dryers and distribution Cooling Water and Cooling Towers Chilled Water Potable Water Domestic Hot Water Safety Shower systems Heat Recovery systems Associated pumps, vessels, heat exchangers, piping, valves, instrumentation, controls/BMS and equipment interfaces
Act as client-side technical lead with project delivery ownership of assigned plant utility systems from construction through startup, commissioning, operational readiness and final handover.
Using strong technical knowledge of system design intent, P&amp;amp;IDs, equipment, piping, controls, interfaces and operating requirements to deliver the systems.
Self starter with the ability to investigate and implement solutions to challenges between design, construction &amp;amp; site operations priorities and the ability to coordinate multiple stakeholders
Using excellent communication skills to manage deliverables and report out on progress including identifying support required, priorities &amp;amp; risks
Provide hands-on field engineering support, monitoring installation and proactively identifying and resolving technical, constructability, quality and operability issues.
Review and resolve RFIs, technical queries, field changes and deviations, coordinating with designers, contractors, vendors and company SMEs as required.
Verify equipment and piping installations against approved design, specifications, vendor requirements and applicable standards.
Support equipment installation, tie-ins, inspections, walkdowns, punch closure and Mechanical Completion of plant utility systems.
Confirm system readiness for pressure testing, flushing, cleaning, filling, water treatment, startup and commissioning.
Coordinate utility interfaces with Electrical, BMS/Automation, HVAC, CSA, Process Utilities and other disciplines.
Provide hands-on startup and commissioning support, working with vendors, Construction, CQV and Operations to troubleshoot equipment and system performance issues.
Verify system hydraulic and operational performance, including flow, pressure, temperature, balancing, controls and equipment operation, and drive deficiencies through to resolution.
Maintain system ownership through operational readiness and transfer of care, custody and control, ensuring outstanding technical and punch items are appropriately closed or managed.
Support Operations and Maintenance readiness, including training, maintenance requirements, vendor support and knowledge transfer, ensuring systems are safe, functional, maintainable and ready for operation. 

 
What you need to apply:

Degree-level qualification in Building Services Engineering, Mechanical Engineering, or equivalent. Professional registration or chartered status preferred but not required.
Minimum 8–10 years of experience in building services design, construction, and commissioning in the life sciences sector.
Comprehensive understanding of MEP systems within GMP and regulated facilities.
Ability to coordinate multidisciplinary engineering teams and lead design reviews.
Strong working knowledge of relevant codes and standards (IS, EN, CIBSE, ASHRAE).
Excellent communication and stakeholder management skills.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Process Scientist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-10-01 14:09:47]]></date><referencenumber><![CDATA[1863]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1863&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Process Scientist for our client based in Mayo. You will be instrumental in maintaining site supply readiness for new products through major and regional market launches, and will lead portfolio change programmes including raw material changes, batch size changes, new technology introductions, and vendor updates.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Provide technical leadership to the Westport site, aligning with the global vision and mission.
Lead and manage cross-functional teams to deliver technology transfer milestones and product launch readiness.
Serve as a primary technical resource for manufacturing issues, driving data-driven root cause analysis and resolution.
Lead complex and high-impact Non-Conformance Reports (NCRs) within the Eyecare portfolio.
Identify, plan, and execute process and technology improvement programmes, including Cost Improvement (CI) initiatives
Lead portfolio change activities such as raw material changes, new technology introductions, and vendor updates.
Represent the site at customer, regulatory-facing meetings, and regulatory audits.
Ensure all activities are carried out in full compliance with GMP and relevant local and global policies and SOPs
Support digitisation of Eyecare and Implants operations and contribute to the Track and Trend programme.
Support Commissioning &amp;amp; Qualification (C&amp;amp;Q) of process equipment in collaboration with Global and Site Engineering.
Drive Process Safety improvements within the Eyecare and Implants operations.
Coach and develop colleagues, fostering a high-performance team culture and promoting cross-departmental training.
Support financial planning activities including budgets, strategic projects, and cost improvement commitments.

 
What you need to apply:

Bachelor's degree or higher in a relevant scientific or engineering discipline; a Master's or PhD in Engineering, Science, or Technology is a distinct advantage. 8+ years of relevant pharmaceutical industry experience (BSc); 7+ years (MSc); 5+ years (PhD).
Demonstrated end-to-end experience of product transfer and launch phases, including regulatory engagements.
Strong technical background in pharmaceutical manufacturing processes, with proven troubleshooting and problem-solving skills.
Excellent leadership, communication, and collaboration skills with the ability to work effectively across Commercial, Operations, Global, and R&amp;amp;D functions.
Comfortable working in a fast-paced, dynamic environment with the agility to adapt to shifting priorities and constraints.

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Manufacturing Specialist ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-10-05 17:10:27]]></date><referencenumber><![CDATA[1864]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1864&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Manufacturing Specialist for an initial 12-month contract. The position acts as a Process Owner Lead and will direct initiatives that improve the reliability and efficiency of manufacturing processes in addition to day-to-day support related to unplanned event troubleshooting, investigations, CAPA identification and implementation.
 
 
Why you should apply:

You will be an established professional who is a self-starter, capable of applying advanced process knowledge and creativity to complete complex assignments related to the manufacturing operations
Hybrid Flexibility

 
 
What you will be doing:

Perform as a knowledgeable subject matter expert (SME), and single point of contact on site and network projects and programs, to advance manufacturing and aseptic operations through ownership of the assigned processes and taking a proactive approach to safety, quality, and compliance by actively seeking opportunities to remove error traps.
Accountable for process documentation (e.g., SOPs, Training, Electronic Batch Records, Risk Assessments) in assigned area of responsibility. Gatekeeper (develop, review and update) of process documentation to maintain structure and control over generation and revision ensuring the documents clearly and correctly direct the process.
Leading and/or providing input to strategic initiatives that will improve and develop processes for the future.
Contribute in a team environment to operational issues pertaining to processes as they arise and provide expertise and support to help resolve escalated technical issues as required.
Use subject matter expertise to identify and lead continuous improvement projects in assigned area of responsibility. Ensure project timelines are met, challenges identified, mitigations are in place and communication plans delivered to all stakeholders.
Involved in the daily business management systems and reporting, have a clear understanding of what is happening in the assigned area of responsibility. Monitor any process trends including business performance metrics. Identify actions that will enable the process and the Manufacturing areas better achieve and surpass metrics in the future.
Lead and/or Support investigations that impact on safety, quality and/or compliance of the processes, ensuring thorough investigations are conducted and actionable CAPAs, to prevent future reoccurrence, are implemented within agreed timeline.
Remain current on state-of-the-art for systems and processes and advise on the appropriate adoption and use of new techniques and technology.
Ability to lead change from an aseptic operations perspective is a plus.

 
What you need to apply:

Bachelor’s degree in Science, Engineering or related discipline with 5 + years’ experience in aseptic Drug Product Manufacturing or related cGxP manufacturing experience.
Experience with regulatory compliance in cGMP manufacturing and in-depth knowledge of Eudralex Volume 4, Annex 1 Manufacture of Sterile Medicinal Products.
Proven ability to work in a high paced matrix organization and effectively influence change and escalate issues professionally and in a timely manner.
Excellent Decision-Making skills and confidence to challenge others respectfully and professionally on decisions that impact the manufacturing area.
Proactive and works well with others in a collaborative, fast-paced goal-driven environment.
Interacts well with diverse groups (Manufacturing, Validation, Engineering, Quality etc) and maintains strong working relationships with internal and external collaborators.
Demonstrated ability to coach, mentor and/or cross train colleagues within core technical areas.
Excellent verbal and written communication skills: Strong Technical writing skills for cGxP documentation (e.g., investigations, procedures, change controls) and good Presentation skills.

 
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Quality, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Contract Manufacturing Sr Mg]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-10-06 15:32:11]]></date><referencenumber><![CDATA[1865]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1865&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CW Contract Manufacturing Sr Mg for our client based in Dublin. Hybrid work with onsite requirement once a month.
 
 
Why you should apply:

This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Manufacturing operations: Develop and lead robust business processes, maintain reliable relationships with contract site management; assess industry trends, internal network, and technology advancements as tools to improve contract site performance.
Manage budget development, monitoring, and reporting; create and manage contracts - confidentiality disclosure agreement(s), scope of work agreement(s), request for pricing/information, supply agreement(s) etc.; monitor and improve financials with CMO; actively manage and communicate forecasts to the sites and manage capacity planning.
Drive operational excellence and champion change.
Site performance monitoring: Manage contract site performance using lean tools and PDCA, lead site operating review meetings; drive improvements at contract sites; sustain and improve the overall health of the business, and lead communication/relationship with the contract site as well as internal management. Project Management and Technology transfer: Lead a department-wide project from conception to implementation and close-out. Present to and obtain buy-in for value proposition of such projects to senior management.
Provide oversight of all planning and coordination of product transfer activities to the contract site(s); develop, present, and obtain approval of budget, timeline and ensure execution of transfer team activities to achieve seamless product transfer to the contract site(s); ensure risk management initiatives are taking place as per RM plan; lead site issue management and resolution; provide issue escalation to executive management.

 
What you need to apply:

Bachelor’s in Business Administration, Engineering, or Science-related field 
8+ years of experience in protein, API, DS, DP, or packaging manufacturing environment 
8+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles 
5+ years of experience working with external parties and/or leading cross-functional teams for clinical and/or commercial products
3+ years of project management experience leading multi-functional and multi-location team 
 3+ years of experience across ACM or CMQ 
Ability to travel +/- 20% of time (domestic and international)    
Assimilates multiple inputs and allocates resources to potentially conflicting priorities     
Anticipates and resolves complex problems and integrates into continuous improvement 
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Management, Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Facilities Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-10-07 12:34:11]]></date><referencenumber><![CDATA[1866]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1866&amp;Itemid=986]]></url><city><![CDATA[Meath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Facilities Technician for a leading pharmaceutical company in Blanchardstown, Dublin. One role is on midweek days and the other is Weekend nights - Friday, Saturday and Sunday – 7pm-7am
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Dublin.

 
What you will be doing:

Work with flexibility within the Engineering Department and in co-operation with other Departments.
Carry out planned and unplanned maintenance on site facilities and utilities equipment.
Report maintenance activities at daily tier meetings, ensuring issues and open items are communicated in a timely and concise manner.
Record maintenance activities in the Computerised Maintenance Management System (CMMS) in detail on facilities and utilities equipment in compliance with regulatory as well as cGMP requirements.
Develop and maintain a good understanding of site utilities, including HVAC, compressed air, MPHW boilers, chillers, purified water systems, fire alarm, BMS and associated controls.
Assist in developing and improving new and existing maintenance plans that are critical to site utilities.
Participate in Safety &amp;amp; Environmental training programmes and initiatives, and adhere to safe working practices as set out by the Safety Statement and other company safety rules.
Take part in cross-functional training initiatives and support training of others as required.
Develop and maintain a strong working relationship with all the departments’ stakeholders on site.
Permit and supervise external contractors on site, ensuring that they adhere to the site safety rules and regulations.
Any other duties as assigned.

 
What you need to apply:

QQI Level 6 electrical trade qualification or equivalent.
A minimum of 5 years’ experience in facilities equipment maintenance.
Experience in Pharmaceutical or related industries preferable but not essential.
Experience in troubleshooting of temperature, humidity, pressure, flow, level, control valves and instrumentation control systems.
Experience in statutory compliance, electrical installation, maintenance and electrical fault finding, electrical testing and verification, statutory testing.
Experience in carrying out preventive maintenance and troubleshooting on facilities/utilities equipment, HVAC, MPHW/LPHW systems, chillers, pumps, motors, compressors, fire alarms, wastewater treatment plants, purified water systems, repair/maintenance of electrical wiring, outlets, fixtures and lighting.
Good Mechanical Aptitude.
Experience in the use of a CMMS system. Proficient in the use of Microsoft 365. Good interpersonal skills. Quality mindset with a focus on detail.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Facilities Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-10-07 12:34:11]]></date><referencenumber><![CDATA[1866-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1866&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Facilities Technician for a leading pharmaceutical company in Blanchardstown, Dublin. One role is on midweek days and the other is Weekend nights - Friday, Saturday and Sunday – 7pm-7am
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Dublin.

 
What you will be doing:

Work with flexibility within the Engineering Department and in co-operation with other Departments.
Carry out planned and unplanned maintenance on site facilities and utilities equipment.
Report maintenance activities at daily tier meetings, ensuring issues and open items are communicated in a timely and concise manner.
Record maintenance activities in the Computerised Maintenance Management System (CMMS) in detail on facilities and utilities equipment in compliance with regulatory as well as cGMP requirements.
Develop and maintain a good understanding of site utilities, including HVAC, compressed air, MPHW boilers, chillers, purified water systems, fire alarm, BMS and associated controls.
Assist in developing and improving new and existing maintenance plans that are critical to site utilities.
Participate in Safety &amp;amp; Environmental training programmes and initiatives, and adhere to safe working practices as set out by the Safety Statement and other company safety rules.
Take part in cross-functional training initiatives and support training of others as required.
Develop and maintain a strong working relationship with all the departments’ stakeholders on site.
Permit and supervise external contractors on site, ensuring that they adhere to the site safety rules and regulations.
Any other duties as assigned.

 
What you need to apply:

QQI Level 6 electrical trade qualification or equivalent.
A minimum of 5 years’ experience in facilities equipment maintenance.
Experience in Pharmaceutical or related industries preferable but not essential.
Experience in troubleshooting of temperature, humidity, pressure, flow, level, control valves and instrumentation control systems.
Experience in statutory compliance, electrical installation, maintenance and electrical fault finding, electrical testing and verification, statutory testing.
Experience in carrying out preventive maintenance and troubleshooting on facilities/utilities equipment, HVAC, MPHW/LPHW systems, chillers, pumps, motors, compressors, fire alarms, wastewater treatment plants, purified water systems, repair/maintenance of electrical wiring, outlets, fixtures and lighting.
Good Mechanical Aptitude.
Experience in the use of a CMMS system. Proficient in the use of Microsoft 365. Good interpersonal skills. Quality mindset with a focus on detail.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Electrical Engineering Advisor]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-10-09 11:33:00]]></date><referencenumber><![CDATA[1867]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1867&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Electrical Engineering Advisor for a major construction projects in Dublin
The project is at construction stage, with the design substantially complete. The successful candidate will play a key role in supporting the client through the construction, commissioning, soft landings, operational readiness and equipping phases of this highly complex healthcare development.
This appointment would suit a senior electrical/building-services engineer who has worked on major, complex construction projects and wants to apply their experience from the client side. The ideal candidate will bring sufficient technical depth to challenge the design and construction teams when required, particularly in relation to critical power, electrical resilience, safety and commissioning, while also understanding that successful delivery of a project of this scale depends on collaboration and effective management of interfaces. Experience of a major hospital project would be highly advantageous. However, candidates from other technically complex sectors such as pharmaceutical manufacturing, semiconductor manufacturing, advanced manufacturing, laboratories, data centres or similarly high-specification facilities will also be considered. A key requirement is the ability to operate effectively from construction through commissioning and into operational readiness, ensuring that the electrical systems delivered are not only technically compliant but are robust, maintainable and fit for the hospital's long-term operational needs.
 
Why you should apply:

Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
They put their people first and live their diversity and inclusion values embracing all perspectives.

 
What you will be doing:

Act as the senior electrical engineering representative within the client project team during construction and delivery.
Provide technical oversight and assurance of electrical installations and associated works.
Review and assess contractor technical submissions, drawings, method statements, technical proposals, commissioning plans and other relevant documentation.
Monitor implementation of the approved electrical design and identify departures, technical risks, interface issues and potential impacts on project performance.
Work closely with the design team and works contractor to resolve technical queries, RFIs, design clarifications and construction issues.
Provide technical input into the management of change, ensuring that proposed changes are appropriately assessed, justified and documented.
Monitor the quality, installation, testing and performance of electrical systems and equipment.
Identify emerging technical, programme, quality and operational risks and ensure that appropriate mitigation measures are developed and implemented.
Support the client team in ensuring that electrical systems are delivered in accordance with the contract, approved design, statutory requirements and relevant standards.
Participate in site inspections, technical audits and quality reviews of electrical installations.
Review inspection and test plans and associated quality documentation.
Monitor installation standards and workmanship and raise technical concerns where required.
Review non-conformances and assist in determining appropriate corrective actions.
Monitor the close-out of technical defects and outstanding works.
Assess the implications of proposed substitutions, alternative equipment and value-engineering proposals.
Ensure that maintainability, accessibility, reliability and future operational requirements are considered during construction.
Provide technical input into risk assessments and project assurance processes.
Provide electrical engineering input throughout the testing, commissioning and integrated systems testing phases.
Review and challenge commissioning strategies, plans, procedures and results.
Ensure that commissioning activities adequately demonstrate the required performance and functionality of electrical systems.
Support the development and implementation of the project's soft landings and operational readiness strategy.
Work closely with the hospital's maintenance and operational teams to ensure that systems are maintainable, accessible and suitable for the intended operational environment.
Ensure that commissioning activities demonstrate not only individual system performance but also the integrated performance and resilience of the hospital's electrical infrastructure
Support the development and review of operation and maintenance documentation, asset information, training requirements and handover documentation.
Assist with the transition from construction into operational use and support the resolution of defects and outstanding commissioning issues.
Work closely with the project team and clinical/operational stakeholders during the equipping phase to ensure that the electrical infrastructure is ready to support the installation and operation of medical and specialist equipment.
Reviewing electrical requirements associated with medical equipment and specialist installations.
Coordinating equipment power requirements with the design and construction teams.
Ensuring appropriate capacity, resilience, isolation and protection arrangements are provided.
Supporting equipment installation, testing and commissioning activities where they interface with the building electrical systems.
Provide expert advice on electrical building-services requirements relevant to major healthcare developments.
Demonstrate a strong understanding of relevant Irish and European standards, legislation, codes and guidance relating to electrical building services.
Have a working knowledge of relevant NHS Health Technical Memoranda (HTMs) and Health Building Notes (HBNs) and their application to healthcare environments.
Ensure that appropriate healthcare engineering principles are considered in construction, commissioning and operational-readiness activities.
Maintain awareness of emerging standards, guidance and best practice relevant to healthcare engineering and complex building-services installations.
The successful candidate will operate at the interface between a number of senior stakeholders, including: Client project and technical teams; The multi-disciplinary design team; The main works contractor and specialist electrical subcontractors; The hospital's maintenance, estates and operational teams; ICT and technology stakeholders; Commissioning specialists; Other technical consultants and advisers; and Relevant statutory and regulatory stakeholders.
Establishing effective professional relationships across the project team.
Providing clear and authoritative technical advice to the project M&amp;amp;E Lead and wider client team.
Facilitating resolution of technical issues between designers, contractors and operational stakeholders.
Participating in design, construction, commissioning and project progress meetings.
Clearly communicating complex technical matters to both technical and non-technical stakeholders.
Supporting the client in protecting the project's quality, programme, cost and operational objectives.
The successful candidate will contribute to ensuring that: Electrical installations are delivered in accordance with the approved design and project requirements.

Critical electrical infrastructure provides the required levels of resilience and reliability. Construction-stage technical issues are identified and resolved efficiently. Electrical systems are appropriately inspected, tested, commissioned and integrated. Emergency and essential-power systems are comprehensively tested. Defects and outstanding technical issues are effectively managed through to completion. Operational and maintenance requirements are incorporated into the delivery process. Hospital maintenance and operational teams are adequately engaged and prepared for occupation. Medical equipment and specialist systems can be successfully integrated with the building electrical infrastructure.
 
What you need to apply:

QQI Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) or equivalent qualification in Electrical Engineering, Building Services Engineering or related discipline.
Chartered Engineer status, or equivalent professional qualification, preferably with Engineers Ireland or an equivalent recognised professional body.
Significant post-graduate experience in electrical engineering and building-services delivery.
Substantial experience working on large-scale, complex construction projects.
Proven experience in a client-side, consultancy, contractor or technical assurance role through construction and commissioning.
Demonstrable experience with complex electrical systems.
Experience of construction-stage technical review, inspection, commissioning and handover.
Strong knowledge of relevant Irish and European standards and requirements applicable to electrical building services.
Working knowledge of NHS HTMs and HBNs, particularly those relevant to healthcare engineering and hospital environments.
Experience of working collaboratively with multidisciplinary design teams, contractors and specialist subcontractors.
Excellent communication, technical-reporting and stakeholder-management skills.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Mechanical Engineering Advisor]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-10-09 12:36:45]]></date><referencenumber><![CDATA[1868]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1868&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Mechanical Engineering Advisor on a major construction project in Dublin
The project is at construction stage, with the design substantially complete. The successful candidate will play a key role in supporting the client through the construction, commissioning, soft landings, operational readiness and equipping phases of this highly complex healthcare development. To provide electrical engineering leadership and technical assurance throughout the delivery phase, ensuring that the electrical building-services systems are delivered to the required standards, performance criteria, quality and operational requirements. This appointment would suit a senior electrical/building-services engineer who has worked on major, complex construction projects and wants to apply their experience from the client side. The ideal candidate will bring sufficient technical depth to challenge the design and construction teams when required, particularly in relation to critical power, electrical resilience, safety and commissioning, while also understanding that successful delivery of a project of this scale depends on collaboration and effective management of interfaces. Experience of a major hospital project would be highly advantageous. However, candidates from other technically complex sectors such as pharmaceutical manufacturing, semiconductor manufacturing, advanced manufacturing, laboratories, data centres or similarly high-specification facilities will also be considered.
 
Why you should apply:

They put their people first and live their diversity and inclusion values embracing all perspectives.
You enjoy working in a culture of learning and collaboration and making a positive impact.

 
What you will be doing:

Act as the senior electrical engineering representative within the client project team during construction and delivery.
Provide technical oversight and assurance of electrical installations and associated works.
Review and assess contractor technical submissions, drawings, method statements, technical proposals, commissioning plans and other relevant documentation.
Monitor implementation of the approved electrical design and identify departures, technical risks, interface issues and potential impacts on project performance.
Work closely with the design team and works contractor to resolve technical queries, RFIs, design clarifications and construction issues.
Provide technical input into the management of change, ensuring that proposed changes are appropriately assessed, justified and documented.
Monitor the quality, installation, testing and performance of electrical systems and equipment.
Identify emerging technical, programme, quality and operational risks and ensure that appropriate mitigation measures are developed and implemented.Support the client team in ensuring that electrical systems are delivered in accordance with the contract, approved design, statutory requirements and relevant standards.
Participate in site inspections, technical audits and quality reviews of electrical installations.
Review inspection and test plans and associated quality documentation.
Monitor installation standards and workmanship and raise technical concerns where required. Review non-conformances and assist in determining appropriate corrective actions.
Monitor the close-out of technical defects and outstanding works.
Assess the implications of proposed substitutions, alternative equipment and value-engineering proposals.
Ensure that maintainability, accessibility, reliability and future operational requirements are considered during construction.
Provide technical input into risk assessments and project assurance processes. Commissioning and Operational Readiness
Provide electrical engineering input throughout the testing, commissioning and integrated systems testing phases.
Review and challenge commissioning strategies, plans, procedures and results.
Ensure that commissioning activities adequately demonstrate the required performance and functionality of electrical systems.
Support the development and implementation of the project's soft landings and operational readiness strategy.
Work closely with the hospital's maintenance and operational teams to ensure that systems are maintainable, accessible and suitable for the intended operational environment.
Ensure that commissioning activities demonstrate not only individual system performance but also the integrated performance and resilience of the hospital's electrical infrastructure.
Any other duties assigned.

 
What you need to apply:

QQI Level 8 (or higher) Quality &amp;amp; Qualifications Ireland (QQI) or equivalent qualification in Electrical Engineering, Building Services Engineering or related discipline.
Or Chartered Engineer status, or equivalent professional qualification, preferably with Engineers Ireland or an equivalent recognised professional body.
Significant post-graduate experience in electrical engineering and building-services delivery.
Substantial experience working on large-scale, complex construction projects.
Proven experience in a client-side, consultancy, contractor or technical assurance role through construction and commissioning.
Demonstrable experience with complex electrical systems.
Experience of construction-stage technical review, inspection, commissioning and handover.
Strong knowledge of relevant Irish and European standards and requirements applicable to electrical building services.
Working knowledge of NHS HTMs and HBNs, particularly those relevant to healthcare engineering and hospital environments.
Experience of working collaboratively with multidisciplinary design teams, contractors and specialist subcontractors.
Excellent communication, technical-reporting and stakeholder-management skills.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job></source>
