<?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[Manufacturing Shift Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2024-04-17 11:03:34]]></date><referencenumber><![CDATA[1244]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1244&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Manufacturing Shift Manager for our client based in Mayo. In this role you will lead and facilitate the safe operations of the 24/7 Biologics manufacturing team in a bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements.
 
This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation.
 
As part of your new and exciting role you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build a culture of high performance for the 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, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

Act as key point of technical contact for aseptic fill finish activities.
Supervision and execution of compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and support processing activities in the biologics fill finish facility to meet clearly stated operating objectives
You will lead, coach &amp;amp; mentor your manufacturing team, across a 12-hour rotating shift, to maximize the effectiveness through clear and effective communication of task details and goals to their team members, to allow the biologics technicians to work effectively
As part of this diverse and inclusive team, you will conduct on the floor promotion of a culture of contamination control and compliance with aseptic best practice.
Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
We believe in collaboration so in this role, you will liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
Resolve operations/project issues by working with team members, project customers, and others as appropriate.
Responsible for driving operations excellences and Key operations targets including OEE where applicable
Provides direct interface as a subject matter expert with QA department to interaction with HPRA, FDA and applicable health authority and internal audits

 
What you need to apply:

Minimum of 3 year’s experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry. 
3rd level qualification in a Science, Engineering or related scientific field, advanced degree is preferred
Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing. 
Has a technical background in pharmaceutical, biologics, or similar industries 
A minimum of 1 year team direct supervisory experience in a team environment
Flexibility with working 12-hour shift, rotating between days and nights on a monthly rotation
Possess a strong technical knowledge and application of concepts, practices, and procedures.
Works on problems of complex scope where analysis of situations or data involves multiple competing factors.
Exercises judgment and advises management as to the appropriate actions

 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></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[Property Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-01-22 16:46:20]]></date><referencenumber><![CDATA[1502]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1502&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Property Manager for a client based in Galway. The Property Manager will be responsible for providing expertise, advice and support services in respect of the management of the extensive property portfolio for the area. The successful candidate must be capable of working on their own initiative, of performing as part of a team and engaging with internal and external stakeholders to deliver property services to our clients.
Why you should apply:

Competitive salary and a 24 month contract
This role offers an opportunity to influence and innovate in the management of critical health estates. If you’re passionate about leveraging your expertise to make a meaningful impact, this is a perfect career move for you!
You enjoy collaborating with cross functional teams, and in this role you get to work closely with local authorities, stakeholders, and multi-disciplinary teams to align property strategies with organisational goals.

What you will be doing:

Provide property management and advisory services as appropriate in the management of the Health Estate  
To assist in the planning management and rationalisation of the existing Estate
Provide, or arrange provision of independent expertise in property valuations.
Ensure yearly updating of property valuations of all properties listed in the Property Registers and Database where required
Advise on strategies associated with potential for disposing of surplus lands and properties, with particular reference to ‘campus’ sites and underutilised properties.
 Advise on strategies to maximise the operational and financial potential of properties and land assets within the portfolios
Review and advise, from a property management perspective, on third party proposals on behalf of clients, e.g. developer proposals, D&amp;amp;B development options, PPP procurement etc.
To advise and assist the integrated service area personnel on the sourcing and acquisition of new facilities in line with the goals contained in their Service Plans
Provide support role and assistance to the  business management personnel in the  integrated service area regarding the Development strategies for campus sites o Strategies for property asset management o Co-ordination of service location planning with Local Authority development planning
 Provide advice and assistance to the Hospitals, Health Community Areas &amp;amp; Corporate in relation to   sourcing suitable properties, through public and private development opportunities, public/private partnership, leasing, renting and buying opportunities joint venturing etc.
Co-operating and liaising as necessary with members of the staff as appropriate in the procurement, planning and zoning relating to buildings and properties
Prepare reviews and commentaries on Development Plans of the Local Authorities within the area, in consultation with appropriate officers and advisors.
Ensure statutory compliance in respect of Planning and Zoning Regulations regarding all properties
Sit on teams convened by the clients, from time to time, in respect of property related proposals
Ensure that property related contracts are executed in accordance with the requirement of the companies Property Protocol
Carry out property suitability assessment reports and liaise as necessary with other internal and external expertise.
Provide documentation in relation to the acquisition and disposal submissions to the Property Review Group and the Senior Leadership Team 
Establish and advise on costs as they relate to property transactions and development proposals
Inspect and review of leases and contracts as required.  Arranging for preparation of title maps, lease maps and other maps associated with contract documents for property related transactions and application submissions to the Property Registration  Authority
Ensure that property consultants, including conveyance solicitors and planning advisors, are fully and clearly briefed as appropriate
Ensure that property transactions and proposals are completed within acceptable time limits in accordance with the property protocol
Advise the Estate Manager as appropriate, in relation to the formulation and review of policies and programmes for property procurement, disposal and development and to ensure that such policies and programmes are communicated and agreed.
Work with the Property Services team and other team members as appropriate and necessary
Build relationships, in order to support the role,  with Estate Agents, Local Authorities and property management personnel
Provide expert advice to the companies personnel  in relation to property matters
Ensure satisfactory progress of property related proposals and transactions and that appropriate information sessions, briefing meetings and consultations are held as required.
Provide timely management information reports as directed by the Estate Manager
Maintain a comprehensive property register database for the company
Such other duties as the Estate Manager may direct from time to time
To act as spokesperson for the organisation as require
Demonstrate pro-active commitment to all communications with internal and external stakeholders
Adequately identifies, assesses, manages and monitors risk within their area of responsibility.
Engage in the companies performance achievement process in conjunction with your Line Manager and staff as appropriate.
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.
Support, promote and actively participate in sustainable energy, water and waste initiatives to create a more sustainable, low carbon and efficient health service
The above Job Specification is not intended to be a comprehensive list of all duties involved and consequently, the post holder may be required to perform other duties as appropriate to the post which may be assigned to them from time to time and to contribute to the development of the post while in office. 

What you need to apply:

Level 8 (or higher) Quality &amp;amp; Qualifications Ireland major academic award in Property Studies, Property Valuation &amp;amp; Management or Property Economics OR appropriate Membership of the relevant professional association: Society of Chartered Surveyors in Ireland OR hold a qualification at least equivalent to one of the above.
Minimum of 7 years relevant experience in the direction and supervision of commercial agency, property valuation, property transactions and/ or property management.
Experience in financial planning, budgeting, lease management and asset strategy development / management.
Broad knowledge of general property management skills across varying markets with experience in Health or other public service desirable
High level of technical proficiency to enable communication in technical terms with relevant personnel
High level of proficiency in valuation &amp;amp; negotiation skills
A knowledge of property procurements options &amp;amp; methodologies within the Public Sector
Good knowledge of zoning and planning objectives, to include development plans &amp;amp; area plans.
Has the capacity to lead, organise and motivate staff and teams to function effectively in times of rapid change.
]]></description><salary><![CDATA[75000]]></salary><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering, Commercial]]></category></job><job><title><![CDATA[R&amp;D Product Technical Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-02-26 14:18:24]]></date><referencenumber><![CDATA[1525]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1525&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[R&amp;amp;D Product Technical Manager
Team Horizon is seeking a R&amp;amp;D Product Technical Manager for a client in Galway. The product Technical Manager is accountable for the deliverables of R&amp;amp;D due to ensure the success of the project. As well as the detailed scheduling and budgeting of R&amp;amp;D activities with support of “Disciplines”)
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.
Excellent contracting rates on offer.
They put their people first and live their diversity and inclusion values embracing all perspectives.

What you will be doing:

Apply the specific PDP of his/her PG/PL following CPM (CLEAN Project Management)
In charge of the robust design in line with the economical targetsApplies Standardization rules, exceptionally will request de standardizations based on sound justifications
Call for all necessary design reviews
Make sure that Design Reviews of other networks are happening in a timely manner (Purchase, Industrial)
Represent the R&amp;amp;D function at the customer
Interface with the customer for the R&amp;amp;D subjects of the project, break down and cascade internally customer requests and needs
Report  and escalate to his project manager or R&amp;amp;D manager as needed
Responsible for the detailed scheduling and budgeting
Contribute to the identification of the needs in terms of resources, equipments, investments
Establish detail break down of the activities to meet the milestones
Follow activities and spending of his scope to meet his allowed budget
Management of the contributors
Daily management of all R&amp;amp;D contributors, dedicated or not
Assign to them the work packages needed
Regular review with his/her R&amp;amp;D manager or Product Manager and the Discipline Department Managers to check alignment between needs and availabilities

What you need to apply:

An Engineering Degree in a relevant area 
Minimum 5 years experience in an Project/Product Management role
Experience in any or all Mechanical, hardware &amp;amp; software design/ technology would be advantageous
Knowledge of engineering drawings &amp;amp; drawing control is desirable but not essential
Technical background Mechanical or Hardware
Good knowledge of design validation (DV) &amp;amp; process validation (PV) programs.
Experience in the automotive Industry will be an advantage
Manage Communication/reporting with customers
Proven ability to deliver projects on time and within budget
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></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]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-09 17:10:58]]></date><referencenumber><![CDATA[1650]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1650&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Project Engineer 
 Team Horizon is seeking a Project Engineer for a client in Mayo. The Project Engineer is responsible for safely coordinating and leading projects associated with New Product Introductions, Process Improvements, Automation, Aseptic processing, New Processing equipment with some Facility / utilities modifications to incorporate same.
 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:
People

Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. Processing equipment would include e.g., Autoclaves, RABS &amp;amp; Isolator Filling machines, LAF units, Compounding skids, Vessels, Containment booths &amp;amp; Stopper processing eq.
Writing User Requirement Specifications.
Selecting Vendors and completing Vendor evaluation matrix
Writing RCE's, placing orders, Project Management &amp;amp; Design review meetings.
Working to the ASME BPE 2019 Standard and relevant ISPE Guidelines etc.
Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel.
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.

Product

Contribute to a team environment on specific technical problem-solving forums associated with Product manufacture &amp;amp; Aseptic fill.
Deliver on Process improvement / cost reduction projects.

Meetings

Lead your regular weekly / bi-weekly Project review meetings with your Project team.
Attend the weekly Tier 1 meeting with your manager.

What you need to apply:
Education and Experience/Knowledge: 

Third level qualification in an Engineering or equivalent discipline/experience.
Experience of working in Biologics, Pharmaceuticals or Medical device industry. Minimum of 2 to 5 years’ experience.
Project Management experience with a 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.

Behaviours/Value: 

 Relationship Building: Establishing working relationships with main contacts through a hands on approach and giving clear and concise instruction.
Communication: Good communication and presentations skills, both written and oral – ability to present data in a clear and concise manner to team members and where required, to management.
Planning &amp;amp; Organising: Able to plan activities and tasks whilst ensuring the required number of people are available and in place to perform the task.
Decision Making: Identify and understand issues, problems and opportunities whilst working within a team environment to provide a solution.
Adaptability; Able to work in a fast, dynamic, environment whilst being able to adjust readily to meet unexpected constraints.
Passion for results: Drive, high energy, and ability to work under pressure and deliver results; get things done (an action-oriented approach) overcome obstacles.
Receptivity to feedback - Receptive to the ideas of others and welcome and accept constructive feedback.
Culture fit: Have a people centred approach in a team environment whilst upholding the values and ethos of the company.

Other requirement (i.e. travel) 

Undertake any travel that the role may require for design review meeting, build inspections, Factory Acceptance Tests (FAT’s) etc.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-10 09:53:08]]></date><referencenumber><![CDATA[1651]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1651&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Sr Project Manager
Team Horizon is seeking a Sr Project Manager for a client in Dublin. The Senior Project Manager will lead project teams and interact across functional and site department groups to achieve project objectives. With minimal guidance, the candidate will lead all aspects of their project(s): Safety, planning, cost, schedule, risk, communications, resources, team dynamics and performance, implementation, monitoring, completion and follow-up.
 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:

Project management and execution of projects including project planning/scoping and execution, prioritization, resources management, status management and external communication.
Working with various stakeholders, both inside and outside to scope projects and ensure requirements are satisfied. Managing expectations and communicating project progress and challenges to these stakeholders.
Develop and/or review engineering technical specifications and bid documents for engineered equipment, materials engineering, and construction service contracts
Lead day to day design (where applicable) and construction management of project works, including procurement, installation, and commissioning
Provide engineering support for manufacturing processes and equipment within the manufacturing facility by designing, specifying, purchasing and constructing mechanical systems and components (with the aid of an A&amp;amp;E firm if required).
Implement and maintain quality control processes to ensure that installations and deliverables meet industry standards and client expectations.
Strategic solution seeking to complex project phasing and execution issues. The Project Manager will be responsible for their portfolio of projects from concept, through design, construction, commissioning and operation
Coordinating the introduction of new equipment including driving the project team problem solving and troubleshooting process prior to qualification &amp;amp; start-up
Leader of multidisciplinary site teams
Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.
Role model safety leadership. Support a safe working environment by driving compliance with environmental health/safety practice, rules and regulations. Ensure projects are designed with superior levels of environmental control, health and safety built in.
Supervise contingent workers as needed. These workers include construction managers and all general craft labour and A&amp;amp;E firm personnel
Present projects to senior leadership at governing bodies for updates and approvals
Limited travel may be required to support execution of projects.

 What you need to apply:

Bachelor’s Degree in Engineering or Relevant Experience
Typically 5+ years project management/engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment
Proven project management experience from project inception through to handover
Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous
Demonstrated experience in a GDP Compliant environment.
Proven ability working cross functionally, delivering technical solutions and implementing improvements.
Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results
Technical report writing and communication/presentation skills
Data driven decision maker
Ability to work to tight deadlines in a fast-moving environment

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></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[Senior System Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-09-18 14:01:24]]></date><referencenumber><![CDATA[1658]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1658&amp;Itemid=986]]></url><city><![CDATA[Limerick]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Senior Systems Engineer
 Team Horizon is seeking a Senior Systems Engineer for a client in Limerick. The Senior Systems Engineer will lead the definition, design, and verification of complex electromechanical systems, translating user needs into system specifications, performing risk assessments (dFMEA), and executing verification and validation activities.
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:

Provides technical solutions to a wide range of difficult problems. Solutions are imaginative, thorough, practical, and consistent with objectives. Exercises latitude in determining technical objectives of the assignment methods and in selecting techniques and evaluation criteria for obtaining resolution based on risk-based assessment (including dFMEA analysis and input into product Hazard Analysis).
Contributes to the completion of specific programs and projects, and develops work plans to reduce concept to design.
Owns derivation &amp;amp; test of product requirements and high-level design system and subsystem specifications. This includes derivation from user needs, writing, tracing, characterizing, and verifying specification performance.
Assumes a technical contributor role and works closely with other functional groups. Will provide guidance and work direction to cross-functional team members including mechanical engineers, reliability engineers, software developers, and software test.
Independently evaluates problems of high complexity and applies analytical/scientific principles to fulfill project and business objectives. Designs and performs development activity independently with minimal supervision.
Development of detailed subsystem workflow step and exception logic to guide software in development of instrument functions as well as to inform Theory of Operation for product/solution. Collects, records, analyzes, interprets, reports, and, presents results to cross functional colleagues and leaders.
Responsible for employing DFSS (Design for Six Sigma) and product development best practices to manage technical risk and impart product robustness and reliability.
Execute system verification and validation activities for their cross-functional project team including protocol writing, execution and reporting.
Contributes to the transition from R&amp;amp;D to manufacturing/service and supports system troubleshooting activities for products in the field.
Liaison between R&amp;amp;D and Quality/Reliability functions to inform/support functions based on quality procedures including risk analysis, verification/validation for specific subsystems.

What you need to apply:

Bachelor’s degree in science or engineering is essential.
A minimum of 6 years relevant experience in systems engineering, medical device design, robotic system design or similar. 
Experience with Systems Engineering and requirements management, including: 

Demonstrated capability with requirement/specification management 
Systems integration and testing, Failure Modes Effects Analysis, verification &amp;amp; validation
Experimental design, data acquisition, graphical analysis and use of statistical methods for large complex data sets.
Experience implementing Design for Six Sigma (DFSS) methodologies.
Beta-testing, and/or field implementation of new product launches preferred. 
Ability to work independently and as a member of a multi-disciplinary team, with global collaboration and external development partners. 
Ability to communicate concepts, ideas and knowledge effectively and clearly to other individuals and teams. 
Experience operating in at least 1 product development process: waterfall or agile; experience operating within design control. 
A differentiator would be an understanding of or experience working in outpatient, retail, and/or central pharmacy.


]]></description><salary><![CDATA[70,000]]></salary><jobtype><![CDATA[Permanent]]></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[Automation Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-10-29 10:53:53]]></date><referencenumber><![CDATA[1682]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1682&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Automation Engineer 
Team Horizon is seeking an  Automation Engineer who will be  responsible for supporting the Business Unit / Department with day-to-day automation issues to ensure successful delivery of the planned production schedule. The primary role is to support the business unit across all shifts and work closely with the Snr Automation engineers for complex issues and identifying process improvements.
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:

Primary responsibility is to support the business Unit / Department with day-to-day automation issues to ensure successful delivery of the planned production schedule. The role will be based on 3rd shift (00:00am to 08:00) @ 33%, with cover support for weekend callouts.
Implementing improvements to the equipment and procedures used in the manufacturing process
Lead small automation projects to improve the processes within the unit
Support the automation design element of capital expenditure projects in the unit/department
Support the installation and commissioning of automated equipment onsite
Contribute in a team environment on specific technical problem solving forums associated with product manufacture, aseptic fill and Packaging
Work closely with the BTS (IT) and Maintenance groups when troubleshooting issues on equipment and systems
Support off shift and weekend issues as required based on a Rota
Attend twice-weekly Tier 2 department meetings             
Attend external meetings as required

What you need to apply:

Bachelor’s degree required in Engineering, I.T, Mechatronics or other related discipline
Minimum 1- 3 years’ experience working on support automation control systems and client/server architectures with a strong grasp of basic networking concepts
Experience working with Siemens and Rockwell (Allen Bradley) PLC control systems
Experience working with SCADA systems, Rockwell FactoryTalk, Siemens WinCC, iFix, Wonderware etc.
]]></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[2025-11-03 10:17:41]]></date><referencenumber><![CDATA[1683]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1683&amp;Itemid=986]]></url><city><![CDATA[Wexford]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[ Facilities Technician 
 Team Horizon is seeking a Facilities Technician for a client in Enniscorthy. This person will perform preventative maintenance on equipment and troubleshoot problems. Repair equipment and systems when they break and must document everything actioned.
 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:

Conduct work on Electrical systems, BMS Systems, HVAC, Boiler Control Systems and emergency lighting systems and process / manufacturing equipment.
Complete work on building services including Mechanical, Electrical, Fire Systems, Building Fabric, etc.
Conduct Mechanical and Electrical maintenance including fault finding.
Completion of facility repair work (General day to day facility maintenance and repairs)
Liaise with supplier and contract companies to ensure maintenance and calibration activities are completed on time.
Ensure all contractors on site are compliant with onsite Health and Safety and GMP standards and procedures.
Participate on project teams with engineers, technicians and other professionals of various disciplines/departments to continuously improve our manufacturing environments and processes.
Support facility validations and manufacturing area qualifications as required.
Manage the CMMS system for all facilities and utilities assets and instruments
Update the plant calibration and preventative maintenance schedules as required for new equipment or updates on existing equipment

Other Responsibilities may include, however are not limited to:

Support other functions in software validation of equipment controls such as Building management systems, facility controls, process equipment controls, HR administrative systems etc.

What you need to apply:

Successful completed a Trade’s Certificate or qualified in a technical discipline.  Fundamental understanding of mechanical, electrical and other utility systems. 
Up to 2 years Electrical &amp;amp; HVAC facilities experience, with high levels of flexibility and innovation. 
Experience in Facility Equipment fault finding and maintenance activities. 
Knowledge of Electrical systems, BMS Systems, HVAC, Boilers, Boiler Control Systems and emergency lighting systems. 
Experience in building services (Mechanical, Electrical, Fire Systems, Building Fabric, etc) 
Excellent interpersonal skills and self-motivated.  Excellent report writing and PC literate. 
Cleanroom experience is an advantage but not essential. 
Ability to assess urgency and impact (e.g., safety-critical vs. routine maintenance).
]]></description><jobtype><![CDATA[Permanent]]></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[Capital Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-04 15:21:39]]></date><referencenumber><![CDATA[1686]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1686&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Capital Project Engineer for a company with projects in Sligo.
The role is to plan and supervise the execution of major &amp;amp; minor capital works.
 
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.
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:

Assist in the preparation of comprehensive brief for the proposed major and minor capital projects in consultation with services and Capital &amp;amp; Estates personnel and advisors.
Prepare budgets for the carrying out of the proposed Minor &amp;amp; Major Capital work programmes and ensuring that projects are within agreed budgets.
Be responsible for Minor Works lists, selection of contractors for bid purposes and recommendation of tenders for acceptance for all projects.
Ensure compliance with EU procurement and company financial regulations.
Supervise staff and contractors in the implementation of the agreed programme.
Provide Technical Support role to service personnel and other Capital &amp;amp; Estates personnel as required.
Prepare in consultation with appropriate officers and advisers, programmes for the maintenance of buildings, services, and equipment (under their control):
Defining in accordance with overall guidelines, maintenance requirements of all buildings, services, equipment, major &amp;amp; minor capital works, fire precautions and risk management schemes and proposing priorities in the allocation of resources.
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 same
Draw up, or in appropriate circumstances, to arrange for the development of plans and contract arrangements for the implementation of approved maintenance programmes:
Assisting in defining requirements for all equipment and building, especially in seeking ease of maintenance and operation.
Recommending awards of maintenance contracts to outside contractors where for economical or practical considerations such is considered desirable.
Developing proposals with selected contractors.
Supervising staff and contractors in the implementation of the agreed programme.
Ensure that the buildings, services, and equipment under their control are adequately maintained in accordance with approved maintenance programmes.
Assist in defining requirements for all equipment and building especially in seeking ease of maintenance and operation.
Comply with regulatory requirements including permission, licences, certificates and approvals.
Work with and support the activities of the Property Manager to ensure compliance with Property Transaction Protocols and other relevant property related task when assigned.
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
Work with the property manager to ensure that all property transactions conform to statutory requirements Assess the physical infrastructure of the companies property portfolio including purpose, state of upkeep, capacity, suitability, space utilization and security
Ensure that adequate fire prevention and safety measures and standards are devised and applied in association with Fire &amp;amp; Safety Officer:
Evaluate environmental infrastructural risk issues &amp;amp; develop procedures to manage risks.
Evaluate the intended performance and operation of healthcare buildings, their actual performance, and to seek continuous improvement through investigation, communication, training, maintenance and review procedures.
Provide advice on the efficient use of energy and work with service personnel and other Capital &amp;amp; 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.
Assisting in the preparation and implementation of 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.
Assisting as necessary in assessing Health &amp;amp; Safety of facilities and environmental risks.
Co-operating with company 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.
Support, promote and actively participate in sustainable energy, water and waste initiatives to create a more sustainable, low carbon and efficient health service.
Adequately identifies, assesses, manages and monitors risk within their area of responsibility.
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.
Succeed in developing good working relationships with other members of the team and with administrators of institutions in which maintenance staff are engaged.
To support, promote and actively participate in sustainable energy, water and waste initiatives to create a more sustainable, low carbon and efficient health service.
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).
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.
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, Building Surveying, Property Surveying or Project Management Division).
Demonstrate a good knowledge and experience of the construction and maintenance of buildings, equipment and services and building regulations and guidelines.
Demonstrate Technical skills and ability appropriate to the post and the ability to motivate staff in safety measures.
Demonstrate knowledge and awareness of EU Procurement legislation and Government construction procurement guidelines.
Demonstrate knowledge and awareness of Health &amp;amp; Safety legislation and 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.
Demonstrate an awareness of the complex service requirements of Health Buildings.
Demonstrate awareness of sustainable Healthcare Building Guidelines and management in the specification design construction and refurbishment of Healthcare Buildings.
Demonstrate evidence of computer skills including use of Microsoft  Word, Excel, email, Engineering specific programmes such as Project Manager, Autocad etc. and Financial systems (for e.g. SAP).
Demonstrate evidence of effective planning and organising skills including awareness of resource management and importance of value for money, the ability to manage deadlines and effectively handle multiple tasks.
Demonstrate leadership and team management skills including the ability to work with multi-disciplinary team members and also the ability to motivate, train, develop and manage staff.
]]></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[2025-11-05 12:01:59]]></date><referencenumber><![CDATA[1687]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1687&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Process Engineer for a leading manufacturing company in Mayo
The company are seeking a Process Engineer to join our engineering team. This is an exciting time to join our team as we bring new products and technologies to the site. The Process Engineer is responsible for providing technical assistance for equipment/machinery and all aspects of performance around the production and packaging of products to meet customer requirements, FDA, HPRA, EPA and safety 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:

Assist with management, engineering, process improvement, equipment reliability, and control system activities.
Identify, plan, schedule, manage and communicate on production related projects to all affected stakeholders.
Ensuring systems, equipment, and products operate at optimal levels and meet Business Unit (BU) needs by preventing failures and maximizing uptime
Analyse equipment failure data, conduct root cause analysis, develop and implement new procedures and processes to prevent reoccurrence
Implement lean technologies such as standard work, visualisation boards.
Support the BU by developing robust process and systems to ensure delivery of effective quality.
Ensure that line processes, equipment and materials are maintained to deliver consistent, reliable and predictable process performance and product quality.
Develop &amp;amp; implement systems &amp;amp; structure to minimise technical downtime on the line.
Resolve technical issues in an effective &amp;amp; timely manner with the technical team to support operations.
Drive continuous improvement and process efficiency programs, i.e., OEE, OPEX, RCA, RCM and productivity output for the BU.
Manage external vendors and services for equipment and technology in the BU along with Manufacturing.
Manage technical documentation, reports, files, logs and records for the BU.
Assist with the trending, monitoring, performance of equipment and the reduction of unplanned downtime.
Help manage, track and monitor the relevant KPIs for the Technical Team.
Assist with the trending, monitoring and reduction of repeat deviations associated with the equipment and technology in the BU. Generate and approve associated change controls and relevant protocols.
Help support the BU during regulatory and compliance audits.
Any other duties as assigned.

 
What you need to apply:

Third level qualification in Mechanical, Electrical or Process Engineering 4+ years experience working in high volume automated manufacturing environment performing a similar role is essential. Pharmaceutical industry experience is preferred.
Detailed knowledge of regulatory requirements in a pharmaceutical GMP environment.
Excellent documentation skills.
Excellent digital literacy with experience using Maximo, One Vault, Quality software and Microsoft Office (Word, Excel, PowerPoint etc.).
]]></description><jobtype><![CDATA[Fixed Term]]></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[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[Health Safety &amp; Infrastructural Risk]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-07 12:37:02]]></date><referencenumber><![CDATA[1690]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1690&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Health Safety &amp;amp; Infrastructural Risk
Team Horizon is seeking a Health Safety &amp;amp; Infrastructural Risk for a client in Galway. This person will provide risk management advice for the protection of staff, public and patients in relation to Infrastructural Risk and Safety issues while ensuring they comply with legal and statutory obligations in relation to Safety and Health &amp;amp; Safety Prevention is met.
Why you should apply:

Competitive salary
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:

Advising as appropriate regarding interpretation of Health Technical Memorandums, Legislation, Guidance &amp;amp; Standards issued by the Government Departments and ensuring their implementation
To monitor the implementation of appropriate and necessary Health, Safety and Infrastructural risk arrangements in respect of the Healthcare Estate and to co-ordinate audits on selected projects
To evaluate the infrastructural risk issues in relation to healthcare estate and to assist in the development of policies and procedures to manage the related risks
To establish and maintain good working relationships with relevant outside bodies, including the Health &amp;amp; Safety Authority and the Health Information and Quality Authority (HIQA), particularly where new standards relevant to Estates Health and Safety and Infrastructural Risks are being considered, prepared or published.
Demonstrate pro-active commitment to all communications with internal and external stakeholders
To assess the continuous professional development and undertake a training need analysis for Estates staff working in this area of Estates.
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.
Assess the continuous professional training requirements for Estates staff in the area and advise the Estate Manager of the appropriate training courses and coordinating with the training providers on the course provided.
Monitor the performance and implementation of the Estates 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 , infrastructural risk and safety matters.
Advise, guide and participate in the risk assessment process/inspection within the area of maintenance and infrastructural risk.
Assist in the development of health and safety training programmes for maintenance
Receive copies of accident reports relevant to their area of expertise, and action/investigate, if necessary. Providing accident investigation reports for accidents investigated.
Have access to the NIMS reporting system and co-ordinate the running of reports on accidents/ incidents within the local estates Office
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 Be a member of the National Health &amp;amp; safety Groups and 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 premises
Assist in the setting up and amendment of Emergency Plans.
Provide an input into planning the Minor Capital Programme in relation to  Infrastructural Risk by highlighting and prioritising essential works required.
Provide guidance and support to Estates staff and Service managers on their obligations with regard to infrastructural risk issues such as Legionella control, asbestos management, radon in buildings and other infrastructural risk items
Assist and provide guidance on the development and implementation of national policies on infrastructural risk and safety issues pertinent to the Capital and Estates function.
Monitor the management of asbestos, legionella, radon, aspergillus and other infrastructural risk issues within buildings under the control of the Estates Office and provide guidance to Service colleagues on their responsibilities

 What you need to apply:

A minimum of 7 years’ relevant experience in Fire Safety or Construction Health &amp;amp; Safety
A Level 8 (or higher) qualification in one of the following areas: Architecture, Engineering, or Surveying (plus a postgraduate qualification in Fire or Health &amp;amp; Safety)
Fire Engineering
Health &amp;amp; Safety (accredited for Graduate Membership of IOSH) OR professional membership with: SCSI, RICS, Engineers Ireland, or RIAI OR eligibility for registration under the Building Control Act 2007
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[EHS]]></category></job><job><title><![CDATA[Robotics Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-12 11:59:07]]></date><referencenumber><![CDATA[1691]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1691&amp;Itemid=986]]></url><city><![CDATA[Ireland]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Robotics Project Engineer
Team Horizon is seeking a Project Engineer for a client in Ireland. This person will support the execution of robotics projects at multiple international sites (Germany, Ireland, Italy, France, Singapore), contributing to planning, implementation, and delivery.
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:

Collaborate with cross-functional site teams to clearly define project scope, objectives, and deliverables that align with both business and technical needs.
Build and maintain strong relationships with site teams, stakeholders, and vendors to anticipate challenges, resolve roadblocks, and ensure successful project outcomes across a range of environments—including highly regulated sectors like Pharma, biotech, or similar.
 Articulate the value proposition and expected benefits of robotics projects, incorporating productivity, efficiency, safety, and (where relevant) compliance considerations.
Manage vendor and third-party relationships covering selection, procurement, and ongoing evaluation of products and services, while ensuring vendors can meet specific requirements of regulated industries if applicable.
Provide hands-on technical leadership to fill capability gaps within project teams, from requirement gathering to solution delivery and troubleshooting.
Identify and assess opportunities for future robotics projects, leveraging best practices from both industrial and regulated environments to build a long-term project pipeline (e.g., 2027 and beyond).
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 (PoC) projects, including piloting new technologies and approaches in various settings such as manufacturing, logistics, or laboratory environments.
Travel as needed, primarily within Europe and occasionally to international sites, with an ability to adapt to diverse regulatory requirements and operational cultures.

What you need to apply:

Background in robotics engineering, sales engineering, applications engineering, or similar functions, ideally with experience across leading robotics platforms (e.g., Kuka, FANUC, ABB, UR, MiR, Otto, etc.).
Proven track record of deploying robotics in manufacturing, logistics, or laboratory processes—converting operational needs into effective automated solutions.
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.
Strong communication and stakeholder management skills, with the ability to work across technical and non-technical teams worldwide.
Adaptive and open mindset, comfortable working in multicultural and multidisciplinary teams, and in both regulated and unregulated environments.
]]></description><jobtype><![CDATA[Remote, 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[2025-11-13 09:51:03]]></date><referencenumber><![CDATA[1693]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1693&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CQV Engineer for a leading pharmaceutical company in South Dublin.
Owns projects, equipment, responsible for document drafting and protocol execution.
 
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:

Single Use / Formulation / Equipment Commissioning and Qualification (C&amp;amp;Q) engineer for a capital project. Ensure the C&amp;amp;Q activities associated with the capital project are completed safely, as per schedule and in compliance with GMP and Quality Requirements.
Commissioning &amp;amp; Qualification of Single Use Systems / Formulation Equipment / Process equipment.
Generation of all C&amp;amp;Q test documents (C&amp;amp;Q Plan/Set to Works/FAT/SAT/IV/FT/C&amp;amp;Q Summary Report.
Provide technical assistance during investigations and system design.
Coordinates and Supervises all C&amp;amp;Q activities on their systems.
Ensures the C&amp;amp;Q schedule is maintained.
Manages Daily C&amp;amp;Q coordination meetings.
Responsible for Tracking and Reporting of C&amp;amp;Q status and risks/issues.
Ensures Startup of equipment/utilities is completed in a safe and coordinated manner.
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:

Commissioning &amp;amp; Qualification of Single Use Systems / Formulation Equipment / Process equipment.
Generation of all C&amp;amp;Q test documents (C&amp;amp;Q Plan/Set to Works/FAT/SAT/IV/FT/C&amp;amp;Q Summary Report
Provide technical assistance during investigations and system design.
Coordinates and Supervises all C&amp;amp;Q activities on their systems.
Ensures the C&amp;amp;Q schedule is maintained.
Manages Daily C&amp;amp;Q coordination meetings.
Responsible for Tracking and Reporting of C&amp;amp;Q status and risks/issues.
Ensures Startup of equipment/utilities is completed in a safe and coordinated manner.
Assist in the development of User Requirement Specifications (URS’s) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).
]]></description><jobtype><![CDATA[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[Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-11-24 12:09:54]]></date><referencenumber><![CDATA[1697]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1697&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[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[CQV Lead]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-04 13:58:00]]></date><referencenumber><![CDATA[1704]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1704&amp;Itemid=986]]></url><city><![CDATA[Westmeath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CQV Lead for a leading pharmaceutical company in Athlone.
We are seeking an experienced Senior CQV Lead to oversee the development and execution of a comprehensive CQV plan for a major upgrade to the manufacturing facility. This CQV lead will be pivotal in ensuring that all systems, equipment, and processes meet regulatory compliance, operational readiness, and project timelines. The Lead CQV Engineer reports to the Engineering Director/Capital Project Lead and is accountable to coordinate CQV resources, deliverables and activities from the validation approach definition, design review, turn-over systems definition and C&amp;amp;Q activities at site.
 
 
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.
You are a project engineer seeking a new challenge and have experience working on a range of projects from the installation of new machinery to the co-ordination of contractors and vendors

 
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 other 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[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[Equipment Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-19 11:14:14]]></date><referencenumber><![CDATA[1707]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1707&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Equipment Engineer for a leading pharmaceutical company in South Dublin
The role is responsible for assisting with the Engineering elements of the expansion project through design, implementation, and operational readiness in collaboration with multiple stakeholder groups.
 
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:

As a member of the Engineering team, support the expansion of the existing manufacturing facility, focusing on filling, inspection, and formulation equipment.
Support the manufacturing readiness strategy, startup, and validation of new systems and equipment to ensure requirements are in line with company standards and fit for purpose.
Assist with equipment project deliverables of setup, calibration, spare parts management, functional testing, and start-up support.
Ensure consistency in equipment design and practices, with a focus on simplifying processes and tasks.
Collaborate with diverse groups including Manufacturing, Quality, PD, Automation, IS, EHSS, and Global Engineering to ensure project delivery.
Establish maintenance strategies and develop initial PM programs for process equipment.
Travel as required to support project execution.
Any duties as assigned.

 
What you need to apply:

Minimum of a Bachelor’s Degree in Engineering (Mechanical, Electrical, or Chemical) with typically 4+ years of experience in engineering projects and systems.
Fundamental knowledge of applicable quality management and regulatory requirements.
Solid leadership, technical writing, and communication/presentation skills.
Experience in change control, non-conformance, corrective and preventative actions, and validation practices.
Experience in developing strategies for new product introduction and new technology deployment.
Team player who actively promotes a culture of clear communication, collaboration, and engagement at all relevant levels for effective decision-making.
Manufacturing experience in a biopharmaceutical formulation/fill/finish facility.
Strong technical ability to understand and resolve complex problems as part of a focused and high-performing team.
Experience in vendor management and contract negotiations with a focus on equipment suppliers.
Independent, self-motivated, organized, and able to multi-task in project environments.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Clerk of Works - Construction]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-22 16:56:45]]></date><referencenumber><![CDATA[1708]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1708&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Clerk of Works for a construction project in Cork/Kerry.
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 - Construction]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-22 16:56:45]]></date><referencenumber><![CDATA[1708-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1708&amp;Itemid=986]]></url><city><![CDATA[Kerry]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Clerk of Works for a construction project in Cork/Kerry.
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[Fire prevention Officer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2025-12-22 17:15:46]]></date><referencenumber><![CDATA[1709]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1709&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Fire Prevention Officer for a company with sites in Cork and Kery
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:

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[Contractor]]></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[2025-12-22 17:15:46]]></date><referencenumber><![CDATA[1709-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1709&amp;Itemid=986]]></url><city><![CDATA[Kerry]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Fire Prevention Officer for a company with sites in Cork and Kery
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:

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[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[ Specialist Data Analytics]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-02 12:01:43]]></date><referencenumber><![CDATA[1710]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1710&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Specialist Data Analytics
Team Horizon is seeking a QC Specialist Data Analytics for our client based in Dublin who will have a key role in  Quality Transformation and the QC Optimization Initiative. The role will be responsible for applying 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:

Analyze and interpret complex QC data from laboratory instruments, manufacturing processes, and digital QC systems to improve decision-making and process efficiency.
Collaborate with QC analysts to design and implement data-driven solutions for quality improvement and regulatory compliance.
Assist in developing business cases and strategic recommendations for digital solution Developments.
Support the definition and advancement of a self-service reporting model. Automate QC reporting and visualization using tools such as Spotfire, Power BI, Tableau to provide real-time insights.
Ensure data integrity and traceability by working with structured and unstructured QC datasets from multiple laboratory sources, including LIMS, LMES, and real-time monitoring systems.
Optimize laboratory workflows by integrating digital tools, AI-driven analytics, and automation to enhance data collection and reporting efficiency.
Partner with business stakeholders to share data best practices, identify and drive business process data standardization initiatives.
Provide support in developing executive communications and present analysis and insights to senior leadership.
Support analytical reports maintenance and validation.
Work closely with IT, data engineering, and digital transformation teams to enhance QC data management and accessibility.
Drive innovation in digital QC strategies, leveraging big data analytics for enhanced quality monitoring and predictive quality insights.

What you need to apply:

Doctorate degree and 2 years of Project Management, Quality and/or Operations experience OR Master’s degree and 6 years of Project Management, Quality and/or Operations experience OR Bachelor’s degree and 8 years of Project Management, Quality and/or Operations experience.
Preferred to have a Bachelor’s or Master’s degree in a relevant field such as Data Science, Chemistry, Biochemistry, Pharmaceutical Sciences, Engineering, or a related discipline.
5+ years of experience in Quality Control (QC) or Manufacturing setting, with a strong focus on QC data analysis and digital optimization.
Deep knowledge of laboratory operations, analytical testing, quality control workflows, and regulatory requirements (e.g., GMP, GLP, FDA, ISO standards).
Proficiency in programming languages with emphasis on SQL, Python and R.
Experience with data visualization tools or packages, such as Spotfire, Power BI or Tableau.
Experience with LIMS, MES, ELN, and other digital QC systems to extract, analyze, and interpret complex datasets.
Strong background in statistical data analysis, process monitoring, and root cause investigations in QC environments.
Experience with advanced statistical/analytical techniques and machine learning algorithms (structured and unstructured data)
Experience with Databricks platform for data analytics and MLOps
Experience working with big data platforms, cloud-based analytics (AWS, Azure, GCP), and automation tools for QC data integration.
Ability to translate complex QC datasets into actionable insights to enhance laboratory efficiency, compliance, and decision-making.
Experience in pharmaceutical, biotech, medical device, or highly regulated industries where QC compliance is critical.
Expertise in data governance, audit trail management, and data security best practices in a QC setting
Expertise in QC technology and digital transformation.
Excellent Organisational, Communication Skills and Time Management.
Ability to work under minimal supervision, identify and manage competing priorities.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Laboratory/Scientific, IT/Software]]></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[CQV Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-06 11:26:44]]></date><referencenumber><![CDATA[1712]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1712&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CQV Engineer for a leading manufacturing company in Mayo.
The CQV Engineer collaborates closely with project teams, contributes to documentation, and actively participates in field execution. This role ensures systems are installed, commissioned, qualified, and validated in line with project requirements, regulatory guidelines, and industry standards.
 
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:

Client-side lead to work with equipment vendors to support the CQV lifecycle activities as part of a new facility start-up project.
Responsible for developing and executing commissioning and qualification documentation for new systems and equipment.
This will include supporting the complete CQV lifecycle; Writing URS documents, review / approval of Design Specifications, input into the control strategy, development and execution of the test matrix (leveraged) to support offsite / onsite execution (as per ASTM E2500).
Participate in and support field execution of commissioning and qualification testing, ensuring accurate data collection, evaluation, and reporting.
Experience of working with equipment vendors to develop and execute the CQV lifecycle.
Assist in troubleshooting, resolution of issues, and investigation of deviations during system start-up and qualification.
Collaborate with engineering, construction, operations, and quality teams to ensure seamless project execution.
Ensure adherence to cGMP, FDA, EU, ISPE, and other regulatory standards relevant to system validation.
Assist with project scheduling, coordination of vendors/contractors, and inventory of required materials/parts for CQV activities.
Maintain robust, compliant, and traceable documentation of all CQV processes.
Identify opportunities for improvement and contribute to best-practice CQV procedures.

 
What you need to apply:

Bachelor’s Degree in engineering or scientific discipline preferred.
Direct experience performing validation studies in cGMP biopharmaceutical or aseptic filling environment is required.
Knowledge of aseptic processing and liquid filling operations preferred.
Must be able to analyse data using basic statistical methods.
3 years of CQV experience in a regulated industry (pharmaceutical, biotechnology, medical device, etc.), covering multiple systems: process, utilities, and/or HVAC.
Demonstrated experience with development and execution of CQV protocols and documentation (FAT/SAT, IQ, OQ, PQ).
Willingness to travel and participate in on-site fieldwork as required.
Solid understanding of process equipment, clean utilities, black utilities, and HVAC system operations.
Strong analytical, documentation, and organizational skills.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-06 14:41:31]]></date><referencenumber><![CDATA[1713]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1713&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[Senior Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-06 14:41:31]]></date><referencenumber><![CDATA[1713-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1713&amp;Itemid=986]]></url><city><![CDATA[Kerry]]></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[Quantity Surveyor]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-06 14:54:23]]></date><referencenumber><![CDATA[1714]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1714&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Quantity Surveyor for nationwide healthcare company based in Galway.
The companies Estate department 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 the health service’s physical infrastructure – including buildings, plant and equipment.
 
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:

Services include design, specification, project management, procurement, contractual, commercial, supervision associated with major and minor capital building and refurbishment works, risk and asset management, property services, fire, health and safety issues etc.
Strategic advice and guidance on the Built Environment in the Healthcare service and related service planning and development issues
Professional technical advice and guidance to the service
Capital programme and project management of same
Procurement of professional design services, construction works and equipment.
Support in the provision and management of estates services through the provision of specific procurement, contractual and commercial related advice and support agreed budgets and agreements at a national, regional and local level, and in compliance with public procurement regulations and other relevant statutory requirements.
Provide professional advice supporting the preparation, management and delivery of the health capital programme.
Provide professional advice on all aspects of procurement, contract, and commercial related issues which related to the delivery of capital projects.
Manage the performance of the appointed Design Team Quantity Surveying consultant in particular to ensure that they are providing the specific deliverables as set out in their agreed scope of service.
Assist in the development of relevant health policies.
Assist with implementation and delivery of national and other priority projects and programmes, in support of approved policy and the service plan.
Prepare standards and guidance for capital investment and development, with particular reference to spatial standards, cost norms, procurement processes and sustainable design.
Promoting achievement of quality in relation to professional services, project outcomes, and sustainable health infrastructure.
Assist with the implementation of a standardised cost reporting structure which will capture key cost, risk, procurement and programme related data which is then reported upon to the Principal Quantity Surveying Adviser.
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.
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.
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.
Assist in the management of projects and helping to quickly resolve such issues as may be for resolution and agreement.
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 company 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 projects, having close liaison with design teams, site supervisory staff, etc. on the one hand and hospital personnel on the other.
Supervising staff and contractors in the implementation of agreed programmes.
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 Principal Quantity Surveying Adviser, and local Estates Leads for decisions on claims for delays, extras etc.
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.
Checking design team fees accounts with regards to agreed fees and certification of same. 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.
Preparation of progress reports on Capital developments
The implementation of Government public procurement policy as advised by the Principal Quantity Surveying Adviser at a regional level.
Promoting effective and efficient capital procurement practices for the selection and contract award of design team and construction services.
Undertaking relevant research and evaluation of completed projects, and to assist in professional development and strengthening of expert capability within the office, as well as the development of a robust and accurate cost database to support in the budgeting preparation for future projects.
Health estate planning, option studies, briefing, design development and project management with a view to optimising value related to best outcomes.
Individual capital expenditure proposals and related whole life cost issues, such as facilities management, maintenance, periodic re-investment and end of use disposal or exit costs.
Maintenance of cost databases, preparing individual project cost limits, assessing of submissions for new capital investments.
Preparing cash-flow forecasting for the respective capital projects as part of the preparation for the quarterly reviews for the management of the Capital Programme / Plan.
Production of guidance material relating to policy delivery, investment, procurement and project management.
Acting as a member of multi-disciplinary project teams for specified projects. Advising design teams in the planning and execution of projects of varying type and scope. Agreeing to and monitoring performance and programme. Ensuring efficient cost management of projects.
Promotion of high standards of cost control practice and procurement process.
Promotion of value for money considerations in the provision of healthcare facilities
Provision of policy advice on relevant investment, cost and procurement issues. Assisting in the development of awareness and understanding of issues and developments in the area of sustainability in energy usage across Health Estate.
Advising on the management of construction and infrastructure risk in health facilities.
Ensuring a pro-active commitment to all communications with internal and external stakeholders. Providing cost, procurement and commercial advice on Sustainability and the efficient use of energy in healthcare premises by:
Understanding the process and procedures around Green Procurement and the implementation of same within procurement strategies and project delivery.
Be familiar with the various form of energy saving technologies and be able to advise on the costs of various energy saving measures Other Duties:
Adequately identifies, assesses, manages and monitors risk within their area of responsibility.
Engage in the company 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.
And another duties as assigned.

 
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 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 officeA knowledge and understanding of the healthcare environment.
A good working knowledge of legislation and technical guidance in the Estates area including Building, Planning, Health &amp;amp; Safety and Fire Safety Regulations.
A knowledge of option appraisal procedures, cost estimation and control, design economics, and the procurement process appropriate to public sector capital projects.
Identifies with and is committed to the core values of the company and places a high emphasis on achieving high standards of excellence.
An understanding of the critical components that make up the health services and their interdependencies that contribute to their successful delivery.
An understanding of the critical issues in relation to the Healthcare Estate.
An understanding of the key issues in relation to capital planning and individual project management.
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering]]></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[Building Services Design Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-07 16:35:57]]></date><referencenumber><![CDATA[1717]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1717&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Building Service Engineer for a design consultancy company with projects in Mayo and Sligo.
This role will be focused on electrical and mechanical design of Building Services including heating, lighting, controls systems, Heat pumps and Boilers systems. The role will be based in Ballina and will include site visits. Project will range from school projects, commercial fit outs and manufacturing projects.
 
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 Design and specification of Electrical Engineering Solutions for Buildings to current regulations and design standards.
Working directly with clients and project engineers to define project requirements and develop technical solutions.
Lead Pre-Construction activities including, design development, construction details, services coordination, technical submittals, sub-contracts, etc.
Provide technical support to the estimating, procurement, commercial, and project bid teams.
Provide off site technical support to construction teams.
Carrying out design and calculation work using relevant industry software (AutoCAD, Revit etc)

 
 
What you need to apply:

Third Level Degree in Electrical, Mechanical or Building Services Engineering.
3+ years’ relevant experience, preferably building services systems.
Strong technical skills in Electrical Engineering Services &amp;amp; Design.
Familiarity with Irish building regulations
Knowledge of Design Guides, Building Regulations, EN &amp;amp; IEC Standards.
Experience with client, vendor, and contractor coordination. Proactive team player with excellent attention to detail.
Proficiency in AutoCAD, Revit, or similar software
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering]]></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[Operations Excellence Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-13 10:47:43]]></date><referencenumber><![CDATA[1719]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1719&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Operations Excellence Specialist for a leading pharmaceutical company in Sligo.
The function of the Operational Excellence Specialist is to support implementation of Lean Six Sigma and continuous improvement programs throughout the organization.
The function of the OpEx specialist is to support implementation of Lean Six Sigma and continuous programs throughout the organization. The job entails supporting internal teams of network change agents to identify opportunities to significantly reduce operating costs, improve efficiency and lead the implementation efforts to achieve these improvements.
 
 
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:
•          Responsible for executing continuous improvement efforts throughout the company to meet service, quality and cost objectives
•          Support excellence in the day-to-day management of the business through implementation and maintenance of daily management tools.
•          Support functional leadership and assigned teams with development of both strategic project portfolios and detailed project plans
•          Establish/maintain network of change agents and be the focal point for continuous improvement expertise and troubleshooting within all support functions.
•          Apply the concepts, tools and training techniques of Lean, Continuous Improvement and Six Sigma philosophies
•          Influence/motivate senior management to identify opportunities and apply Lean, Continuous Improvement and Six Sigma philosophies.
•          Support/motivate project teams to ensure timely and successful delivery of projects.
•          Provide regular communication of project status to departmental staff and leadership
•          Lead education and training, in partnership with the OpEx team.
•          Lead and facilitate process improvements and Structured Problem Solving using Lean and Six Sigma Methodologies Digital experience – power BI Implement Operational Excellence Tools and systems to support the overall site objectives and the achievement of the site Perfect Index Targets.
•          Enhance and improve site performance through the implementation of tools and systems to monitor and deliver key performance metrics.
•          Drive the CI, OpEx culture at the site as a change agent and by engaging employees through programs like 5s, iCAN and Gemba. Deliver training across the site including HER and OpEX and provide mentorship and coaching to employees.
•          Any other duties as assigned.
What you need to apply:
•          Must have a Six Sigma Yellow or Green belt.
•          1-3 years relevant experience in an Op Ex role.
•          A self-starting, self-motivated, leader with highly developed interpersonal skills.
•          Excellent written and oral communication skills, experience in presenting complex data to all levels of leadership Excellent organizational skills, problem solving and conflict resolution, and the ability to develop win/win relationships with other teams and organizations.
•          Strong analytical skills and familiarity with statistical analysis (e.g. Minitab, JMP
 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Equipment Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-13 11:41:33]]></date><referencenumber><![CDATA[1720]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1720&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Equipment Engineer for a leading pharmaceutical company in South Dublin.
The Project / Equipment Engineer reports to the Senior Manager for Strategic Engineering Projects and is responsible for scoping and executing technical projects supporting Drug Product manufacturing within Formulation, Component Preparation, Vial/Syringe Filling, Lyophilisation, Device Assembly, Inspection, Filter/Filter Integrity Testing areas. This includes qualification of new equipment and implementation of associated reliability and maintenance programs. 
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:
•          Project management and execution of assigned projects including project prioritization, resources management, status management and external communication.
•          Working with various stakeholders, to scope projects and ensure requirements are satisfied. Project input will span from concept, through design, construction, commissioning and operation
•          Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification &amp;amp; start-up
•          Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
•          Ability to translate strategic/emerging technology solutions into pragmatic executable plans
•          Development and management of change controls
•          Participate as a member of multidisciplinary site and multisite team.
•          Development of detailed specifications, engineering documents, protocols and standard operating procedures
•          Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.
•          Works in a collaborative manner with the System Owners, Maintenance Supervisors &amp;amp; Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.
•          Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures
•          Support a safe working environment by complying with environmental health/safety practice, rules and regulations
•          Travel may be required to support execution of projects.
•          Any duties as assigned.
 
What you need to apply:
•          Bachelor’s Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience.
•          Typically, 3+ years engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment or Automated Inspection and/or Automated Device Assembly.
•          Proven project management experience.
•          Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous.
•          Demonstrated experience in a GDP Compliant environment.
•          Experience in MS Office, MS Project, Change Control &amp;amp; Document Management Systems.
•          Proven ability working cross functionally, delivering technical solutions and implementing improvements.
•          Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results.
•          Technical report writing and communication/presentation skills.
•          Data driven decision maker.
•          Ability to work to tight deadlines in a fast-moving environment]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Investment Coordination &amp; Operations Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-14 10:51:30]]></date><referencenumber><![CDATA[1721]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1721&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking an Investment Coordination &amp;amp; Operations Specialist for a leading pharmaceutical company in Dublin.
The Dublin manufacturing site is progressing through a period of significant investment and innovation, supported by a broad portfolio of capital projects, R&amp;amp;D initiatives, and transformation programs. The site has secured IDA grant approval and routinely submits R&amp;amp;D tax credit applications to Irish Revenue. To support this work, we are building a team responsible for ensuring investments are well managed, well documented, and fully compliant with funding and regulatory 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 in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

 
What you will be doing:

The Investment Coordination &amp;amp; Operations Specialist will provide the day-to-day organisational, analytical, and documentation support required to keep these processes running smoothly. The role works closely with the Transformation Lead, Finance, Engineering, Operations, and third-party partners to ensure investment activities are efficient, transparent, and aligned with internal and external expectations.
Investment Activity Coordination - Support the planning, organisation, and tracking of site investment activities across capital, R&amp;amp;D, and innovation projects.
Maintain clear documentation on project progress, spend, milestones, and resourcing.
Help coordinate the flow of information and updates between project teams and leadership.
Tracking of Spend, Invoices &amp;amp; Supporting Documentation - Maintain organised records of invoices, purchase orders, expenditure, and relevant documentation associated with investment and R&amp;amp;D activities.
Monitor and record spend patterns and ensure supporting details are available and accurate.
Distinguish and document spend categories (e.g., capital, operational, R&amp;amp;D-related) based on guidance from Finance.
Support the preparation of scheduled spend reports or summaries.
Resource &amp;amp; Activity Allocation Support - Track resource utilisation across relevant projects, including internal labour contributions and contractor involvement.
Maintain logs, trackers, and summaries that support downstream funding applications and internal reporting.
Work with teams to ensure their time and activity records are accurate and up to date.
IDA Grant Support &amp;amp; Drawdown Preparation - Maintain structured, audit-ready documentation required to support IDA grant drawdowns.
Organise and validate the information required for each funding milestone or claim.
Ensure records align with approved project scopes and IDA conditions.
Work with Finance and Engineering to gather supporting materials such as invoices, timesheets, project updates, and evidence of eligible activities.
R&amp;amp;D Tax Credit Preparation &amp;amp; Coordination - Coordinate the annual collation of materials required for R&amp;amp;D tax credit submissions.
Support the gathering of evidence, technical summaries, labour allocations, and eligible spend records.
Work with cross-functional SMEs to ensure documentation is complete, consistent, and compliant with Irish Revenue requirements.
Maintain structured files to support potential Revenue queries or audits.
Governance, Organisation &amp;amp; Process Administration - Maintain templates, trackers, checklists, and logs to ensure investment-related processes are well organised and repeatable.
Help ensure documentation is stored correctly and accessible for reviews or audits.
Contribute to refining and improving internal workflows related to investment tracking, grant management, and tax credit support.
Stakeholder Communication &amp;amp; Administrative Support
Support meeting preparation, including agendas, notes, action tracking, and follow-ups.
Facilitate communication between internal teams and external partners regarding documentation or data needs.
Assist in the preparation of presentations, reports, and executive updates.
Any other duties as assigned.

 
What you need to apply:

3+ years' experience in roles involving coordination, administration, operations, or process support. Strong organisational skills with experience maintaining high-volume documentation or records.
Familiarity with invoices, POs, and basic spend or activity tracking. Strong proficiency in Excel and comfort working with enterprise systems (SAP, Oracle, or similar).
Ability to work collaboratively with technical teams and cross-functional stakeholders.
High attention to detail and a structured, methodical approach to organising work. Desirable  Experience within a biopharmaceutical, pharmaceutical, or regulated manufacturing environment.
Exposure to government funding, grants administration, R&amp;amp;D activities, or tax credit submissions.
Understanding of capital/R&amp;amp;D investment lifecycles or engineering/technical project environments.
Experience with reporting tools (Power BI, Smartsheet, or similar). Competencies  Excellent organisation and documentation discipline.
Strong communication and coordination skills.
Ability to handle multiple streams of information simultaneously. Analytical mindset and comfort working with structured data.
Proactivity, problem-solving, and continuous improvement mindset. High integrity and commitment to compliance.
What This Role Enables  Smooth, organised, compliant administration of IDA drawdowns and R&amp;amp;D tax credit submissions.
Clear visibility and traceability of investment activities across the site. Strong operational support for site transformation, innovation, and growth programs.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Warehouse Specialist]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-19 10:29:01]]></date><referencenumber><![CDATA[1723]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1723&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Warehouse Specialist
Team Horizon is seeking a Warehouse Specialist for a client in Sligo. The Warehouse Department is part of the Supply Chain function with responsibility for the following areas:

Receiving, Material handling and storage, issuance of materials to Production
Packaging and shipping and associated documentation

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:

Maintain a clean and organized work area
Assist our client in achieving environmental, health, and safety goals by working safely and observing all general plant and department safety policies
 Ensure accurate Receipt of Materials in a timely manner
Ensures that all materials are accurately located and controlled both physically and on SAP.
Issuance of material to manufacturing and Packaging
Shipping of product and non-inventory items in accordance with SOPs
Complete area verification in accordance with SOPs and cGMPs. (ie returns/staging/fixed bins etc)
Perform all assigned duties according to departmental SOP's and cGMP's.
Remain current on proper procedures by reviewing current, revised, and new SOP's relating to the job and to the department.
Complete and remain current with all required cGMP and safety training.
Perform tasks in warehouse that complement the manufacturing and business objectives of the Business units and to provide on-time delivery to customers.
Complete all required documentation associated with the supply of materials.

What you need to apply:

Leaving Certificate or equivalent
3 years + industry experience within a warehouse environment, pharma/regulated environment preferred.
High sense of safety standards within a regulated GMP environment.
Experienced computer skills, Outlook, Microsoft Excel. Word &amp;amp; Powerpoint. 
Good Knowledge of SAP and Warehouse processes.
Good Knowledge of Products and processes.
Experienced forklift driver.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Operations &amp; Manufacturing]]></category></job><job><title><![CDATA[Automotive Vehicle Maintenance and Electronic Support Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-19 16:18:07]]></date><referencenumber><![CDATA[1724]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1724&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Automotive Vehicle Maintenance and Sensor Integration Support Technician for a leading automotive company in North Galway.
The primary objective is to ensure our R+D fleet of test and capture vehicles are maintained and operating to the highest standards and available for project engineering and development work. The scope of work encompasses the maintenance, installation, debugging and data handling activities for our ADAS test vehicles and associated equipment.
 
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:

Vehicle Fleet Maintenance: Perform maintenance checks on our test vehicles to ensure maximum availability for test and development work. This includes diagnosing and repairing modern vehicle system faults.
ADAS Hardware Installation: Install ADAS system sensors (e.g., cameras, radars, ultrasonic sensors, LiDARs) into development vehicles. Sanity test and validate to calibration level.
Custom and Integration: Design and build sensor brackets, complete harness builds, and perform fi nal integration testing for all installed ADAS equipment.
Calibration : Sensor calibration after retro to ADAS vehicles
Equipment Management: Build and install ADAS sensor measurement equipment into vehicles.
System Debugging: Support the engineering team in debugging faults related to the systems under test on the vehicles.
Preparation of ADAS vehicles prior to customer or senior management visits for the purpose of a system demonstration.
Test Bench Support: Assist with the building of test benches to validate measurement equipment prior to vehicle installation.
Data Handling: Support the handling and transfer of data storage devices from the test vehicles to the on-site data storage systems.
Documentation: Prepare documentation, reports, and logs related to maintenance, installation, and testing activities.
Any duties as assigned.

 
What you need to apply:

A minimum of five (5) years experience in diagnosing and repairing modern vehicle system faults.
A minimum of five (5) years experience with modern automotive diagnostic tools and vehicle bus protocols/architecture (e.g., CAN, Ethernet).
Excellent communication skills and attention to detail.
Ability to work in a fast-paced development environment and maintain efficiency under pressure.
A valid driver's license with a clean driving record. 6. Familiarity with high-voltage (HV) automotive systems is an advantage.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Equipment Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-20 12:09:04]]></date><referencenumber><![CDATA[1726]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1726&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Equipment Engineer for a leading pharmaceutical company in South Dublin.
The Project / Equipment Engineer to join the facilities &amp;amp; engineering team to support the continued expansion of the plant and production capability on site. The Project / Equipment Engineer will report to the Senior Manager for Facilities &amp;amp; Engineering Projects and is responsible for portfolio ownership, scoping and executing technical projects within Formulation, Component Preparation, Syringe Filling, and Inspection areas. This includes new product introductions, qualification of new equipment and implementation of associated reliability and maintenance programs.
 
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:

Portfolio ownership of a number of projects within a specific business area supported by reporting engineers for successful completion.
Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification &amp;amp; start-up.
Coordination of engineering readiness scoping and readiness for new product introductions.
Project management and execution of assigned projects including project prioritization, resources management, status management and external communication.
Working with various stakeholders, to scope projects and ensure requirements are satisfied. Project input will span from concept, through design, construction, commissioning and commercial operational readiness.
Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
Ability to translate strategic/emerging technology solutions into pragmatic executable plans.
Development and management of change controls.
Participate as a member of multidisciplinary site and multisite teams.
Development of detailed specifications, engineering documents, protocols and standard operating procedures.
Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.
Works in a collaborative manner with the System Owners, Maintenance Supervisors &amp;amp; Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.
Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures.
Support a safe working environment by complying with environmental health/safety practice, rules and regulations.
Travel may be required to support execution of projects.
Any other duties asa assigned.

 
What you need to apply:

The successful candidate for this role will bring the following education, skills and experience
Bachelor’s degree in engineering (Mechanical, Electrical or Chemical) or Relevant Experience.
Typically, 5+ years engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment or Automated Inspection and/or Automated Device Assembly, Labelling and Ancillary processes.
Technology transfer experience preferred.
Proven project management experience.
Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous.
Demonstrated experience in a GDP Compliant environment.
Experience in MS Office, MS Project, Change Control &amp;amp; Document Management Systems.
Proven ability working cross functionally, delivering technical solutions and implementing improvements.
Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results.
Technical report writing and communication/presentation skills.
Data driven decision maker.
Ability to work to tight deadlines in a fast-moving environment.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-20 12:15:47]]></date><referencenumber><![CDATA[1727]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1727&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Manager for a leading pharmaceutical company in South Dublin.
The Project Manager – New Syringe Fill Plant Engineering Readiness will report to the Associate Director. They will be responsible for managing projects within the Operations Readiness Programme for the new fill plant project. The successful candidate will have at least five to eight years of experience within the pharmaceutical or biotech industry and will have demonstrated project management skills.
 
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:
•          Experience in a leadership role in a pharmaceutical or biotech manufacturing facility that engages with site SMEs and managers, and global functions.
•          The ability to influence and lead cross functional teams to deliver their projects that ensure a smooth start up of the new vial filling line.
•          The ability to work independently and identify risks and mitigation pathways to ensure project delivery
•          A passion for continuous improvement applied to project management.
•          Lead and drive Engineering readiness for new filling plant.
•          Arrange agreement among the project team, customers, and management on the goals of the project.
•          Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification &amp;amp; start-up.
•          Works in a collaborative manner with the System Owners, Maintenance Supervisors &amp;amp; Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.
•          Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
•          Works with workstream leads to develop and maintain the Project schedule/plan that aligns with the overall goals of the Programme.
•          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
•          Always ensure compliance to cGMP.
•          Ensure safety &amp;amp; compliance standards are maintained to the highest standards 
•          Ensure financial compliance in line with Business &amp;amp; Financial guidance 
•          Support a culture of personal responsibility within reporting structure 
•          High Energy and Commitment.
•          Ability to work independently.
•          Comfortable leading across multiple stakeholders &amp;amp; multinational teams.
•          Strong ability to influence and affect change.
•          Capable of resolving issues of conflict effectively.
•          A proven track record in the ability to transfer goals and objectives into measurable plans.
•          Ability to identify gaps/risks and put appropriate remediation plans in place.
•          Uses strong relationships to identify requirements and potential opportunities.
•          Employs project management techniques and Problem Solving.
•          Provides leadership, guidance, and advice in own field of project management
•          Knowledge or experience with MES and MBR projects.
•          Knowledge or experience with validation of Aseptic Filling Lines.
•          Any other duties as assigned.
 
What you need to apply:
•          Technical Degree and/or Masters’ or equivalent in Engineering 5-8 years of experience (including min of 2yrs as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment.
•          Preferred Experience: Portfolio Management, Portfolio Resource Management, Business Case Development 
•          Systems / Equipment: MS Office, MS Project, MS PowerPoint and MS Visio, Change Control &amp;amp; Document Management Systems.
•          Preferred Requirements: Smartsheet.]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Equipment Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-20 12:21:15]]></date><referencenumber><![CDATA[1728]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1728&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Equipment Engineer for a leading pharmaceutical company in South Dublin.
The Project / Equipment Engineer reports to the Senior Manager for Engineering Projects and is responsible for scoping and delivering technical projects that support Drug Product manufacturing. The role focuses primarily on the Lyophilisation area, with additional responsibilities across Formulation, Component Preparation, Vial/Syringe Filling, and Inspection. Key responsibilities include the introduction and qualification of new or upgraded equipment, along with the implementation of associated reliability and maintenance programs.
 
 
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:

Project management and execution of assigned projects including project prioritization, resources management, status management and external communication.
Acting on behalf of the sustaining system owners to ensure the robust and effective delivery of project elements to the end user.
Working with various stakeholders, to scope projects and ensure requirements are satisfied. Project input will span from concept, through design, construction, commissioning and operation
Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification &amp;amp; start-up
Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
Development and management of change controls
Participate as a member of multidisciplinary site and multisite team.
Development of detailed specifications, engineering documents, protocols and standard operating procedures.
Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.
Works in a collaborative manner with the System Owners, Maintenance Supervisors &amp;amp; Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.
Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures.
Support a safe working environment by complying with environmental health/safety practice, rules and regulations.
Travel may be required to support execution of projects (e.g. FAT).
Any other duties as assigned.

 
What you need to apply:

Bachelor’s Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience.
Typically, 3+ years engineering experience, preferably in a GMP biopharmaceutical manufacturing environment.
Proven project management experience.
Strong mechanical capability with hands on equipment experience in a technical role.
Demonstrated experience in a GDP Compliant environment.
Experience in MS Office, MS Project, Change Control &amp;amp; Document Management Systems.
Proven ability working cross functionally, delivering technical solutions and implementing improvements.
Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results.
Technical report writing and communication/presentation skills.
Data driven decision maker.
Ability to work to tight deadlines in a fast-moving environment.

 ]]></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[2026-01-20 12:54:02]]></date><referencenumber><![CDATA[1729]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1729&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer for a leading pharmaceutical company in Blanchardstown, Dublin.
Supporting the Capital Projects Team with site-based projects for Oral Solid Dose Manufacturing, Facilities and Packaging operations.
 
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:
•          Supporting the Capital Projects Team with site-based projects for Oral Solid Dose Manufacturing, Facilities and Packaging operations.
•          Supporting and executing validation support activities on site.
•          Partaking or leading potential continuous improvement programs, process mapping and gap analysis.
•          Optimisation of existing processes to achieve desired targets.
•          Delivering projects and assigned duties on time and on budget.
•          Coordinating changes using the approved change control procedure to ensure that cGMP is adhered to.
•          Supporting validation activities for project activities, including the review of validation documentation and attendance of validation activities.
•          Designing and writing summaries for regulatory compliance or project specific documentation, including URS, DS and detailed project schedules using MS Office applications (Project, Word, Excel, Visio, etc.).
•          Updating project details on a regular basis, leading project teams during scheduled project meetings, providing feedback and updates to team and senior management.
•          Any other duties as assigned.
 
What you need to apply:
•          Bachelor’s degree in Engineering.
•          5 years' experience in the Pharmaceutical Industry as a Project Engineer.
•          Experience in cGMP, general packaging systems and serialisation is advantageous.
•          Ability and proven track record of working and managing multiple departmental teams for operational and capital projects.
•          Excellent technical writing ability.
•          Strong documentation skills.
•          Strong interpersonal and communication skills.
•          Must work to the highest engineering standards.
•          Have strong technical and problem-solving skills.
•          Willingness to travel within Europe (minimal travel depending on projects). Hybrid/flexible working.]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></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[Maintenance Engineering Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-22 14:06:09]]></date><referencenumber><![CDATA[1732]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1732&amp;Itemid=986]]></url><city><![CDATA[Meath]]></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[Maintenance Engineering Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-22 14:06:09]]></date><referencenumber><![CDATA[1732-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1732&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[R&amp;D Environmental Test &amp; Validation Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-28 14:26:28]]></date><referencenumber><![CDATA[1733]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1733&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a R&amp;amp;D Environmental Test &amp;amp; Validation Engineer for a leading manufacturing in North Galway.
The Engineer will support DV planning, execution, and reporting. This Engineer will cover all documentation, project management, requirements review, test equipment bring up, testing and reporting across all environmental test activities.
 
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 Galway

 
What you will be doing:

Test service request process, review and analysis.
Analyse customer specification with the product Project Team Member and quality PTM, challenge the tests requested and define the final validation plan to build the final offer. Define the need of specific tools or bench (characterization, reliability...)
Define also the associated budget.
Write the detailed validation plan and test specification including both customer validation and also company requirements (to achieve quality targets)
Schedule the validation plan and manage the test with the support of laboratory resources (technicians…)
Responsible for the main relationship with the customer and project team for environmental validations (methods and results) wherever the tests are located (Troy, Shenzen, Bietigheim, Prague, external lab…).
Work in parallel with the project team; contribute to correct the design in order to meet product performance.
Manage the configuration and logistics of tested parts
Lead validation FMEA generation for assigned project
General DR’s for software, hardware &amp;amp; product design reviews, problem resolution, FMEA analysis. 3)
Manage the planning inside the laboratory and allocated resources (technicians, tools, benches,…)
Responsible to obtain the specific tools needed for the validation (need specification and follow-up).
Manage the cost of the validation activities.
Familiarise with working system using bench equipment to enable view on delivered product and to understand customer problems.
Carry out all work to comply with Quality Management System and Validation Engineering Processes e.g. ASPICE, ISOTS16949.
Work with Methods &amp;amp; Tools (M&amp;amp;T) team to develop test environment solutions to enable Design &amp;amp; Process Validation (DV/PV)
Test setup and verification of test platforms.
Test script development (using NI LabVIEW / TestStand)
Execution of testing using lab equipment (using thermal chambers, IPx) as per test specification
Safety focussed and dedicated to maintaining high quality standards
Report validation status to the project team and management on a regular basis (QRQC, 5mm…)
Generation of test reports, peer-reviews of data and follow up on approval
Create daily and weekly activity report on project and non project related activities using dashboards made available
Perform problem management role interfacing with customer, allocation of Device Under Test (DUT) failures to appropriate functions and leading weekly review
Participate in lessons learned across the various projects

 
What you need to apply:

A relevant Technical Engineering Degree e.g. Computer &amp;amp; Electronic Engineering, Physics &amp;amp; Instrumentation, Mechatronics.
Min 3 years test engineering experience Proficient in National Instruments (LabVIEW/or TestStand) Computer literate in MS Office suite (ECDL)
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[CSV Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-01-28 16:19:56]]></date><referencenumber><![CDATA[1734]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1734&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CSV Engineer for a leading pharmaceutical company in Blanchardstown, Dublin.
 
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:

Support Manage activation and de-activation of accounts for on-site computer systems.
Ensure compliance with local and global SOPs for related CSV activities.
Ensure all associated documentation is managed and executed accordingly.
Liaise with stakeholders ensuring smooth transition to the new account management process.
Work with the CSV support teams to implement relevant aspects of the CSV remediation plan.
React to any access issues in an appropriate timeframe to ensure minimal effect on site operations.
Provide the Senior Engineering Director with regular updates and escalate any issues should they arise.
Support other engineering systems activities when required.
Any duties as assigned.

 
What you need to apply:

Proven Experience working in a Manufacturing or Packaging environment, preferably in a regulated industry.
Experience in generation or modification of setup configuration in equipment computer systems would be an advantage.
An Engineering or IT qualification. A basic understating of Computer Systems Validation.
Experience using other Engineering and Compliance Systems.
Good attention to detail.
Previous experience with GMP document management.
Good communication skills and works well within a team environment.

 ]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Equipment Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-03 14:12:15]]></date><referencenumber><![CDATA[1735]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1735&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Equipment Project Engineer for a leading pharmaceutical company in South Dublin.
The role will be responsible for the Syringe Inspection Equipment elements of the new facility, including implementation and ensuring operational readiness of the equipment.
 
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 role will be responsible for the Syringe Inspection Equipment elements of the new facility, including implementation and ensuring operational readiness of the equipment.
As a member of the Site Engineering team, support the existing manufacturing facility, with a focus on syringe inspection equipment.
Support the manufacturing readiness strategy, startup, and validation of new systems and equipment to ensure compliance with company standards and fit-for-purpose requirements.
Assist with equipment deliverables, including setup, spare parts management, functional testing, start-up support, and sustaining equipment in operation.
Collaborate with diverse groups including Manufacturing, Quality, PD, Automation, IS, EHSS, and Global Engineering to ensure successful project delivery.
Establish maintenance strategies and develop initial preventive maintenance (PM) programs for process equipment.
Any other duties as assigned.

 
What you need to apply:

Bachelor’s degree in engineering with typically 5+ years of experience in engineering projects and systems.
Fundamental knowledge of applicable quality management and regulatory requirements.
Strong leadership, technical writing, and communication/presentation skills.
Experience developing strategies for new technology deployment.
Demonstrated ability to foster a culture of clear communication, collaboration, and engagement at all levels for effective decision-making.
Manufacturing experience in a biopharmaceutical formulation/fill/finish facility.
Strong technical ability to analyse and resolve complex problems.
Experience in vendor management, with a focus on equipment suppliers.
Independent, self-motivated, organized, and able to multi-task in project environments.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Facilities Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-06 11:30:08]]></date><referencenumber><![CDATA[1736]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1736&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Facilities Project Engineer for a leading pharmaceutical company in South Dublin.
Support the Facilities Project Manager in the delivery of Facilities-related capital and operational projects.
 
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:

Participate in the full project lifecycle, including concept development, scope definition, detailed design, execution, commissioning, and close-out, in accordance with the site Engineering Project Delivery process.
Drive the safe execution of works in compliance with site procedures, corporate standards, and applicable regulatory requirements.
Review project works for installation quality and complete system walkdowns, punch-list management, and system turnover activities.
Provide technical and operational support for site Facilities systems, including but not limited to: HVAC System.
Support the operation and maintenance of HVAC systems, including AHUs, chillers, HEPA filtration, isolator air handling, pressure cascades, and environmental control systems.
Apply GMP and regulatory requirements related to temperature, humidity, differential pressure, and cleanroom classification.
Interpret engineering documentation including P&amp;amp;IDs, ductwork schematics, and control logic.
Support monitoring and alarm management through BMS / EMS systems, including calibration and data integrity requirements.
Support the management of mechanical and electrical lift systems, including control panels, safety interlocks, and load requirements.
Act as site SME for warehouse and vertical storage systems including maintenance, operation and lifecycle management.
Ensure compliance with statutory and regulatory requirements (e.g. LOLER, EN81).
Coordinate preventive maintenance activities and contractor oversight.
Review inspection reports, safety certificates, and support resolution of identified non-conformances. Electromechanical Door Systems.
Support electro-mechanical door systems, including sensors, control units, actuators, and safety features.
Assist in troubleshooting issues such as misalignment, sensor faults, or cycle failures.
Ensure systems support GMP material and personnel flows and site segregation requirements.
Support vendor performance management, servicing activities, and documentation review.
Develop, maintain, and continuously improve Facilities preventive maintenance plans.
Utilise computerised maintenance management systems and applications (e.g. CMMS/Maximo) to plan and document technical activities and asset spares management.
Support planning, scheduling, and execution of site shutdowns and outage activities.
Contribute to system reliability, compliance, and inspection readiness
Support cross-functional coordination with Engineering, Quality, EHS, and Operations as required.
Bachelor’s degree in Engineering or a related technical discipline, or equivalent relevant experience.
Minimum 3–5 years’ experience in a GMP-regulated manufacturing environment, preferably biopharmaceutical.
Working knowledge of Facilities systems and infrastructure within a regulated manufacturing site.
Equipment troubleshooting and maintenance strategies and systems.
Strong organisational skills with the ability to manage multiple priorities.
Effective written and verbal communication skills.

 
What you need to apply:

Bachelor’s degree in Engineering or a related technical discipline, or equivalent relevant experience.
Minimum 3–5 years’ experience in a GMP-regulated manufacturing environment, preferably biopharmaceutical.
Working knowledge of Facilities systems and infrastructure within a regulated manufacturing site.
Equipment troubleshooting and maintenance strategies and systems.
Strong organisational skills with the ability to manage multiple priorities.
Effective written and verbal communication skills.
Experience supporting Facilities systems within the pharmaceutical or biotechnology industry.  Familiarity with GMP and Good Documentation Practices.
Experience supporting capital project delivery in an operational manufacturing environment.
Ability to build effective working relationships and partnerships at all levels of the organisation.
Experience working with CMMS systems (e.g. Maximo/SAP).
Strong problem-solving skills and a proactive, self-motivated approach.
Demonstrated leadership potential and a flexible, team-oriented work ethic.
Commitment to treating colleagues, contractors, and stakeholders with dignity and respect.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Maintenance Reliability Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-09 11:54:54]]></date><referencenumber><![CDATA[1737]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1737&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Maintenance Reliability Engineer
 Team Horizon is seeking a Maintenance Reliability Engineer for a client in Dublin. This person will be responsible for improving the reliability, availability, and maintainability of plant equipment and utilities within the manufacturing facility.
The role is responsible for establishing and maintaining a robust reliability framework that enables right-first-time maintenance execution, reduces unplanned downtime, and optimises asset lifecycle performance, supporting safe, compliant, and efficient operations.
 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 Drug Product manufacturing within the Formulation, Vial/Syringe Filling, Lyophilisation and Component Preparation
Employ business analytics to assess performance and identify improvement opportunities for Equipment Reliability, Maintenance Reliable Execution, Condition Monitoring and Predictive Maintenance.
Develop &amp;amp; Design Multi-Year Reliability roadmap and ensure flawless execution with close collaboration/partnership with key cross-functional stakeholders.
Analyse equipment performance data (e.g. downtime, failure trends, MTBF, MTTR) to identify chronic issues and implement sustainable reliability improvements.
Collaborate with system owners, planners, and technicians to define maintenance scopes, refine job plans, and ensure maintenance tasks are technically sound, risk-based, and executable.
Support shutdown and non-commercial time activities by ensuring reliability-critical work is correctly prioritised, scoped, and executed to deliver right-first-time outcomes.
Drive continuous improvement through the cycle, capturing lessons learned and embedding standard work, best practices, and technical documentation into future maintenance execution.
Lead and support system improvements, development of detailed specifications, engineering documents and standard operating procedures.
Solving complex problems, project management, equipment lifecycle management and operational excellence.
Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations.

What you need to apply:
Basic Qualifications 

Bachelor’s degree in Engineering (Mechanical, Electrical, Electronic, Chemical, Software) or equivalent qualification and/or relevant experience.
Minimum of 5 years’ experience in a cGxP manufacturing environment in a maintenance, reliability, or engineering role.
Demonstrated ability to work across functional boundaries and influence outcomes without direct authority.  Preferred Experience
 5+ years’ engineering experience in a pharmaceutical or biotech manufacturing environment.
3 years’ experience supporting aseptic fill / finish or other highly regulated manufacturing processes.
Proven experience implementing reliability improvement initiatives in complex, multi-system facilities. 

Knowledge and Relevant Experience 

 Strong working knowledge of pharmaceutical/biotech manufacturing and aseptic processing.
Fundamental understanding of GxP, EHS, and regulatory compliance requirements.
Asset reliability methodologies (RCA, FMEA, criticality analysis, PM optimisation).
Experience with CMMS/EAM systems (e.g. Maximo) and data-driven maintenance decision-making.
Application of continuous improvement tools and methodologies (Lean, Six Sigma, TPM). 

Skills 

Strong collaborator who promotes a culture of reliability, accountability, and continuous improvement.
Ability to assess and influence both short- and long-term decisions impacting equipment uptime and plant availability.
Excellent analytical, problem-solving, and prioritisation skills.
Strong technical writing and communication skills, with the ability to clearly convey complex technical concepts to diverse audiences.
Ability to balance tactical execution with strategic reliability planning.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Visual Inspection Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-11 11:12:10]]></date><referencenumber><![CDATA[1738]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1738&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Visual Inspection Engineer
Team Horizon is seeking a Visual Inspection Engineer for a client in Sligo to support visual inspection operations.
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 Visual Inspection operations to meet all safety, regulatory, and organizational standards
Develop and optimize procedures to enhance manufacturing processes.
Participate in process, equipment, and facilities validation projects; review and execute commissioning and validation protocols to keep projects on schedule.
Support the introduction of new Semi Automate visual inspection equipment on site and associated training
Lead and facilitate FMEAs for Visual Inspection, and drive the certification of technicians.
Build and maintain defect libraries and execute trending for defect analysis.
Ensure local procedures align with global guidelines and regulatory expectations
Provide technical leadership and guide the development of SOPs for visual inspection.
Collaborate with internal and external stakeholders to evaluate particles/defects and support technical transfers for new product introductions.
Investigate process deviations and support the production team in achieving output and yield targets.
Ensure full compliance with quality, safety, cGMP, and regulatory policies.
Supervise external contractors as required.

What you need to apply:

Hold a Level 8 degree (or higher) in Engineering, Science, or a relevant technical discipline. 
Minimum 3 years' experience in a biotech or pharmaceutical manufacturing environment—experience with biotechnological drug processes, fill finish, lyophilisation, and sterilisation preferred. 
Strong problem-solving and innovative thinking skills under pressure.
Familiarity with Semi Automated Visual inspection equipment 
Exceptional attention to detail and commitment to quality.
Excellent communication and interpersonal skills; proven ability to work both independently and in cross-functional teams.
Leadership qualities with a results-driven mindset. 
Demonstrate integrity, a strong work ethic, and the ability to work autonomously. 
Familiarity with cGMP, ISO, FDA regulations, and EHS best practices preferred.
]]></description><jobtype><![CDATA[Permanent]]></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[Project Engineer - Mechanical &amp; Electrical Design]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-12 10:20:15]]></date><referencenumber><![CDATA[1740]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1740&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer - Construction Design for a leading pharmaceutical company in South Dublin
This job description is for a Project Engineer with previous relevant experience to provide client side design input at the Basis of Design, Detailed Design, Commissioning, Qualification and handover stages of a design project for a Pharmaceutical facility. Particular relevance would be previous experience in Large Scale Capital Projects, in Biologics, Pharma or fill/finish Facilities.  The scope of the role, may also require / includes design input and support during the project phases for various ancillary areas such the existing Warehouse, general site infrastructure, which are all collectively managed as part of the project.
The position is a hybrid position with an on-site (3 Days) and remote working element.
As design progresses, attendance at A&amp;amp;E offices will also be required, and these will count as on-site days. Due to the nature of the role, the Project Engineer will also be required to support the design process with potential visits to design offices.
 
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:

To support client side design team in its efforts associated with the design of the new Facility and ancillary projects (Laboratory reconfiguration, Canteen expansion and Warehouse Modifications) as directed by the Design Manager.
To coordinate client side design activities by liaising with Design Team Resources, Site SME’s and Client’s Engineering Technical Authority (ETA) in delivering the Canteen and Laboratory designs.
To partake in client side design reviews and to coordinate the participation of all stakeholders.
To coordinate and participate in cross functional package, area, or overall design team reviews as required in support of client’s overall design goals and expectations
To support site facility and utility walkdowns by the third Party designers and to schedule such activities with site Facilities Group, Engineering and the Laboratory End-User.
To act as a point of contact for all technical queries in relation to assigned scopes of work
To manage / monitor project action logs / RFI’s / review cycles
To be available to execute scopes of work (Manage / Coordinate) in support of the overall project schedule. (Knowledge of CE Marking / Legislation would be an advantage)
To coordinate with Site Facilities, Engineering and End Users in relation to the Site Engineering Change Management process.
To liaise with C&amp;amp;Q, in support of the commissioning / qualification of the Laboratory and Canteen systems.
To support the handover process of the systems / facilities to Engineering and Laboratory End-Users.
Any other duties as assigned.

 
 
What you need to apply:

Minimum of 5 years of experience in pharmaceutical Facility, with experience of Engineering Documentation Management, Project Execution and/or Facility Design.
Ability to challenge, defend and present technical aspects of design and commissioning.
Good communications skills.
An understanding of interdisciplinary interfaces and an ability to resolve conflicting prioritiesDegree level qualification in Mechanical, Electrical Engineering, CSA background, or similar/equivalent.
]]></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[2026-02-12 11:11:58]]></date><referencenumber><![CDATA[1741]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1741&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a CQV Engineer for a manufacturing company in Sligo.
The CQV Engineer will be responsible for planning, generation, execution and reporting of  Commissioning, Qualification and Validation (CQV) of facility, utilities and process equipment. This role will support both new and legacy equipment.
 
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:

This role is an individual contributor role whereby the individual must be a self-starter with significant professional experience design, commissioning, qualification and continuous improvement of pharmaceutical facilities, utilities and equipment.
Prepare, execute and report on CQV activities for assigned systems to include C&amp;amp;Q Planning, URS generation, DQ facilitation, TM/RTM, FAT, SAT, IQ, OQ and where applicable PQ activities.
Prepare, review and approve project documentation, ensuring technical accuracy and adherence to cGMP.
Support design reviews and system risk assessments with multiple stakeholders.
Confirm all vendor documentation executions are compliant with GxP practices and the executed documentation is acceptable to support CQV.
Complete field verifications during static and dynamic (functional) tests.
Participate in startup activities of energized equipment when necessary.
Interaction with vendors for project planning.
Perform system P&amp;amp;ID walkdown with construction prior to handover. Categorization of punch list items &amp;amp; tracking to completion.
Support review on all Isometrics, Weld logs, Weld Qualifications, 3rd Party Inspections, Material of Construction and Redlining exercise.
Confirm the site installation is as per approved design specification and meet system IQ requirements.
Facilitate/expedite Mechanical Completion in conjunction with the Construction team. (Liaise with construction contractors towards successful completion of Construction Turn Over Documentation).
Assist in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents.
Manage project change and CQV discrepancies through close interaction with System User and Quality Assurance.
Support the handover of contractor and vendor systems to the user.
Ensuring that all vendors and sub-contractors assigned to the specific tasks are trained and have experience to carry out tasks.
Liaise with the various stakeholders on the Project team and the overall project to ensure clear communication between all parties.
Participation in and execute design reviews (DQ), when required.
Review and Input into deliverables such as technical requirement specifications and vendor turnover documentation.
Manage the site attendance for the vendors, contractors and specialist contractors.
Liaising with Construction management team to ensure completion of mechanical completion packs, review of all contractors packs for traceability, review of all supporting vendor documents in timely manner to support execution.
Where necessary attendance at FAT’s at Vendor Sites anticipated to be in mainland Europe.
Any other dutes as assigned,

 
What you need to apply:

A minimum of an Honours degree in an Engineering or Science discipline.
At least 3 years’ experience in the biotechnology and/or pharmaceutical industry, in a CQV role.
Proven experience in authoring, review and execution of CQV activities on a variety of Facility, Utility and Process Equipment is essential.
Experience with clean utilities and aseptic processing facilities would be an advantage.
Experience in Computer Systems Validation is desirable.
Experience in temperature mapping of temperature control devices and sterilization cycles is desirable.

 ]]></description><jobtype><![CDATA[Permanent]]></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[2026-02-16 15:20:07]]></date><referencenumber><![CDATA[1742]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1742&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is recruiting on behalf of a global manufacturing organisation for a Process Engineer in Galway. The role will support and improve automated production within a high-volume electronics environment.
This is a hands-on role focused on process ownership, equipment performance, and continuous improvement within a fast-paced production setting.
This opportunity suits a proactive, floor-focused engineer who enjoys solving technical production challenges and driving measurable performance improvements. The role involves evening and night shifts.
 
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:

Own and improve manufacturing processes and production equipment.
Drive OEE improvements and structured problem solving (8D / DMAIC / PDCA).
Support process validation, documentation, and engineering change management (ECR/ECO).
Implement lean manufacturing principles (5S, Kanban, takt time optimisation).
Participate in design reviews to ensure manufacturability.
Support quality investigations and implement permanent corrective actions.
Ensure processes are maintained to internal and external audit standards.
Any other duties as assigned.

 
What you need to apply:

Degree in Manufacturing, Mechanical, Industrial, Electronics, Computer Science or related Engineering discipline.
2+ years’ experience in electronics or high-volume manufacturing.
Experience working with automated production systems
Knowledge of APQP, PPAP, PFMEA, OEE and lean methodologies
Exposure to structured change management in a production environment
Experience in the following would be helpful: Python / C++ / Java / NI LabVIEW / NI TestStand, PLC coding.
Experience with high-speed data systems or embedded hardware environments
AI or machine learning exposure
]]></description><jobtype><![CDATA[Fixed Term]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Electrical Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-18 10:01:06]]></date><referencenumber><![CDATA[1743]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1743&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Electrical Engineer for a leading pharmaceutical company in North Dublin.
Acting as the site Electrical systems SME, develop and put in place a structured Electrical (preventative/Predictive) Maintenance Program for the site, in compliance with European Electrical standards &amp;amp; ETCI rules &amp;amp; Regulations, aligned with European Electrical standards. To ensure the site electrical infrastructure is set up on the site Maximo CMMS to be maintained according to industry’s best standards.
 
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:

Project: Lead, develop and implement a site Electrical Maintenance program.
Identify all HV, MV and LV Electrical systems and infrastructure on site.
Develop a site electrical hierarchy architectural A-CAD drawing, identifying from incomer to lowest level sub boards – maintain consistent labelling of same and implement PM’s for all panels &amp;amp; distribution boards.
Develop a site life support systems hierarchy architectural A-CAD drawing, identifying top tier boards to lowest level sub boards – maintain consistent labelling of same and implement PM’s for all panels &amp;amp; distribution boards. This is specific but is not limited to Emergency lighting, fire alarm, O2 detection systems and LEL systems.
Update Maximo CMMS with each Electrical system/asset, as per site MEP guidelines.
Document and implement preventative maintenance job plans for each electrical system on the Maximo CMMS, to ensure the site electrical systems are maintained in compliance with European electrical standards and ETCI rules and regulations.
Document and implement an approved site Electrical systems Maintenance SOP, aligned to with European Electrical standards.
Responsibility for the upkeep of the electrical SOP.
Identify and develop a maintenance program for all electrical PPE safety equipment and test equipment.
Implement and maintain an electrical manual/handover pack library.
To ensure the site electrical systems are maintained/upgraded in compliance with European electrical standards and ETCI rules and regulations.
To keep up to date with latest technologies &amp;amp; updates to electrical standards.
To manage and co-ordinate the site efforts in planning and executing a site electrical power down/up ensuring work is GMP &amp;amp; safety compliant with minimal impact to site activities.
Own and manage the associated site change control and relevant stakeholder meetings.
As required, provide support to all electrical activities and assigned multi-disciplinary projects.
Engage as the point of contact for all Project electrical works.
Develop a handover index requirement and review all project electrical hand over packs.
To maintain and update all site electrical drawings to as built.
To maintain the site ARC flash study/short cct capacity study and incorporate additional upgrades.
To maintain the ARC flash panel signage is kept up to date and current for the electrical infrastructure – maintaining electrical infrastructure safety signage and minimum PPE requirements for entry to the restricted boundaries.
To develop and maintain a site ATEX register.
To develop a site ATEX PM program in line with European standards.
To review all ATEX PM reports.
To identify and manage ATEX PPE requirements &amp;amp; ATEX tools inspection PM’s.
To develop a site minimum IP rating map for all site electrical infrastructure.
To represent the electrical program during FM Global inspections.
To engage in developing/maintaining an Electrical network throughout the company.
To provide condition reports in relation to the following systems and follow up to ensure the applicable maintenance program is put in place.
Oversee and ensure repairs are completed correctly and systems remain within compliance with European electrical standard requirements: - MV circuit breakers &amp;amp; transformers - LV circuit breakers - LV bus couplers - Power Factor Correction - Active Harmonic filters - UPS systems - Lightening protection system - Surge protection devices - Emergency Lighting system (EN3217) - General Lighting - Fire alarm system (EN3218) - Power Quality system - Energy Monitoring system - CCTV system - Security systems - Street lighting - Site Generator - Thermographic surveys - Variable speed drives - PAT testing - MCC Drawers - Electrical switch rooms - Electrical cabinets – site wide - ATEX register
To recommend actively pursue Electrical infrastructural improvement.
Has set targets and goals to achieve which are reviewed on a weekly basis.
Incumbent receives only general instructions from management personnel as to manner to which duties should be performed.
Incumbent is charged with responsibility for project management on electrical utilities, and electrical lead on all site-based projects.

 
What you need to apply:

Qualifications: Bachelor’s Degree: Electrical or Mechatronic Engineering (OR) National Craft Certificate in Electrical Engineering &amp;amp; Degree in Management
10 years plus of Experience as an Electrician.
Required to correctly identify and assess site electrical installations to ensure specifications are correctly identified.
Required to implement industry best practices for maintenance of each electrical system/asset in compliance with European electrical standards and ETCI rules and regulations and European Electrical standards.
Ensure new electrical projects are risk assessed, value engineering is incorporated.
Input to design in new equipment, energy, electrical, instrument project upgrades and installations as projects dictate.
As SME for site Electrical systems maintenance standards.
Ensure that project meets compliance, regulatory &amp;amp; stake holder expectations.
Manage project to ensure that schedule, quality, cost, and safety requirements are achieved.
]]></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 Operations Aseptic Specialist for our client based in Sligo. As a member of the Aseptic Operations function, and as an Aseptic Manufacturing SME, ensures that procedures related to Aseptic Manufacturing are in compliance with relevant Regulatory requirements and Network Best Practice.  Partners with Site colleagues and other members of the Site Aseptics team, to create an environment of the highest standards of Aseptic Manufacturing.  Drives continuous improvement in Aseptic Manufacturing on site.
 
 
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:

Acts as a site Subject Matter Expert for Aseptic Manufacturing.
Provides key input for setting up the Manufacturing process.
Provides key input for the Manufacturing Batch Record.
Responsible for ensuring that Operations procedures required for Aseptic Manufacturing are in compliance with relevant Safety and Environmental Regulations, Aseptic and GMP Regulatory requirements and Network Aseptic Best Practice.
Ensures appropriate use of Risk Management tools to drive Aseptic performance/ Sterility Assurance.  Responsible for completing pFMEA and What If/ HAZOP assessments.
Partners with other members of the Site Aseptics Team (e.g. Quality SMEs, Engineering SMEs, Aseptic MQA and Aseptic mentors) to ensure required support is provided to manufacturing shifts to ensure safe, quality, and timely completion of product batches in an aseptic manner, assuring sterility of the product. 
Drives a high-performance culture in Aseptic Manufacturing, through communication and colleague engagement.  Drives a culture of Speak-Up.
Routinely observes the Aseptic technique and behavior of the shift team, providing feedback as appropriate, in particular during critical Aseptic activities such as Cleaning, Sanitization, Aseptic Set-up, EM plate handling and Interventions.
Actively leads and supports investigations into process/product issues in support of sterility, media fill, environmental monitoring excursions and EMPQ and assists with establishing root cause and CAPA.
Owns analysis and trending of EM data (Facility and Personnel) including ownership of the EM Visualization tool and its standardized use across functions.  Develops and executes action plans to address EM trends.  Provides key input to EM procedures.
As part of the Site Aseptics Team, drives continuous improvement of Aseptic Manufacturing procedures through:  a) Continuously assessing, interpreting, and applying new Aseptic Manufacturing Regulations to Site operations in a timely manner. b) Development and implementation of Best Practices in Aseptic Manufacturing.
Ensures that all procedures and changes follow Site Change Control procedures.
Provides key input into the Site Contamination Control Strategy.
Provides key input into site APS strategy.
Provides key input into Site LRP related to Aseptic Manufacturing.
Provides key input into Cleanroom/ Equipment/ Utility design, Qualification and Re-Qualification processes, Preventative Maintenance strategies and real-time monitoring.
Supports regulatory audits as Aseptic/ Sterility Assurance subject matter expert
 Supports training of Operations personnel in Aseptic technique and in Aseptic processing related procedures.
Participate in routine leadership GEMBAs of Manufacturing and Testing areas.

 
What you need to apply:

Third Level Degree in a Science, Quality or Engineering discipline.
5+ Years of experience in a GMP Environment with 3+ years of experience in support of Aseptic Manufacturing (non-negotiable)
Strong knowledge of Regulatory Requirements including EU GMP Annex 1 'Manufacture of Sterile Medicinal Products,' FDA requirements including 21 CFR Part 610 (General Biological Products Standards), 21 CFR Part 210 (Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs) and 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals) and FDA guidance documents such as 'Sterile Drug Products Produced by Aseptic Processing—Current Good Manufacturing Practice.'
Author and subject matter expert for risk management tools that drive aseptic performance / sterility assurance including contamination control strategy, pFMEA, HAZOP, What if?
Experience in tracking and trending environmental monitoring data as microbial subject matter expert. 
Experience in investigations into process/product issues in support of sterility, media fill, environmental monitoring excursions and EMPQ and assists with establishing root cause and CAPA.
Excellent communication skills

 
 ]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[Engineering]]></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[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 Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-02-26 10:45:19]]></date><referencenumber><![CDATA[1750]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1750&amp;Itemid=986]]></url><city><![CDATA[Westmeath]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[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[Project Manager]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-03 11:52:54]]></date><referencenumber><![CDATA[1751]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1751&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Manager for a leading pharmaceutical company in South Dublin.
This role will work closely with the Engineering Technical Authority (ETA), Site Engineering, Manufacturing, Quality, and external vendors to ensure projects are delivered safely, compliantly, on schedule, and within budget. The Project Manager will coordinate a cross functional team and is responsible for, coordinating technical, operational, CQV and External Suppliers.
This role reports directly to the Engineering Technical Lead for the Formulation and Component Preparation Area.
 
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:

Project Leadership &amp;amp; Delivery: Lead end to end delivery of Formulation and Component Preparation Area from design through construction, CQV, and handover to operations.
Develop and manage project scope, schedule, cost, risk, and resource plans, ensuring alignment with business objectives.
CrossFunctional &amp;amp; Stakeholder Management: Act as the primary interface between ETA technical leads, site engineering, manufacturing, quality, EHS, digital, and supply chain.
Coordinate and align equipment vendors, engineering firms, and contractors to ensure delivery against agreed milestones and quality standards.
Compliance, Quality &amp;amp; Safety: Ensure project execution complies with cGMP, EHS, and corporate engineering standards.
Support and oversee CQV activities, ensuring readiness for commercial operation.
Promote a strong safety culture throughout design, construction, and commissioning phases.
Financial &amp;amp; Risk Management: Manage capital budgets, forecasts, change control, and cost reporting.
Proactively identify and mitigate technical, schedule, cost, and compliance risks.
Ensure effective vendor performance management and contract execution.
Digital &amp;amp; Sustainability Focus:
Integrate digital manufacturing, automation, and data strategies into project delivery.
Champion sustainable design choices, energy efficiency, and resource optimization in line with sustainability goals.
Any duties as assigned.

 
What you need to apply:

3-5+ years of experience in capital project delivery within the biopharmaceutical, pharmaceutical, or highly regulated manufacturing industry.
Proven experience managing end-to-end facility or manufacturing area projects (concept through design, construction, CQV, and operational handover).
Demonstrated experience delivering projects within GMP-regulated environments.
Experience managing capital budgets, cost forecasting, changing control, and risk management for complex projects.
Excellent communication and stakeholder management skills in a collaborative, matrixed environment.
Direct experience supporting or overseeing Commissioning, Qualification, and Validation (CQV) activities.
PMP (Project Management Professional), Chartered Engineer (CEng), or equivalent professional certification is desirable but not required.  
Bachelor’s degree in engineering (Chemical, Mechanical, Electrical, Biochemical, Process, or related discipline).
Advanced degree (MSc, MEng, MBA) is desirable but not required.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Project Manager - Operational Readiness]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-03 12:56:39]]></date><referencenumber><![CDATA[1752]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1752&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Senior Project Manager for a leading pharmaceutical company in South Dublin.
The Snr Project Manager will be responsible for managing projects within the Operations Readiness Programme for the new fill plant project. The successful candidate will have at least five to eight years of experience within the pharmaceutical or biotech industry and will have demonstrated project management.
 
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:

Experience in a leadership role in a pharmaceutical or biotech manufacturing facility that engages with site SMEs and managers, and global functions.
The ability to influence and lead cross functional teams to deliver their projects that ensure a smooth start up of the new vial filling line.
The ability to work independently and identify risks and mitigation pathways to ensure project delivery.
A passion for continuous improvement applied to project management.
Lead and drive Engineering readiness for new filling plant.
Arrange agreement among the project team, customers, and management on the goals of the project
Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification &amp;amp; start-up.
Works in a collaborative manner with the System Owners, Maintenance Supervisors &amp;amp; Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.
Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
Works with workstream leads to develop and maintain the Project schedule/plan that aligns with the overall goals of the Programme.
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
Always ensure compliance to cGMP
Ensure safety &amp;amp; compliance standards are maintained to the highest standards
Ensure financial compliance in line with Business &amp;amp; Financial guidance
Support a culture of personal responsibility within reporting structure.
Any other duties as assigned.

What you need to apply:

Technical Degree and/or Masters’ or equivalent in Engineering.
5-8 years of experience (including min of 2yrs as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment.
Preferred Experience: Portfolio Management, Portfolio Resource Management, Business Case Development.
Systems / Equipment: MS Office, MS Project, MS PowerPoint and MS Visio, Change Control &amp;amp; Document Management Systems
Preferred Requirements: Smartsheet
Knowledge or experience with validation of Aseptic Filling Lines
Proven experience leading full equipment introduction projects in the pharmaceutical sector.
Strong technical background (likely engineering degree or similar).
Demonstrated leadership in cross-functional/technical teams.
Good understanding of project delivery phases from concept to operational readiness in GMP environment.
Capable of both high-level project oversight and hands-on technical interventions.
Experienced in reviewing/creating URSs, understanding vendor management, and site readiness documentation.
Familiar with communicating with design, CQV, and sustaining engineering teams. Nice-to-Haves
Experience in filling/packaging operations—ideally with syringe lines or cold-chain/freezer installs.
Previous capital project delivery experience.
Experience working with external vendor partners and managing multiple streams of workstream delivery.
Knowledge of clean and/or plant utilities.
]]></description><jobtype><![CDATA[Contractor]]></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[2026-03-03 14:21:18]]></date><referencenumber><![CDATA[1753]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1753&amp;Itemid=986]]></url><city><![CDATA[Cork]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Fire Prevention Officer for a company with sites in Kilkenny and South East.
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:

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[Contractor]]></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[2026-03-03 14:21:18]]></date><referencenumber><![CDATA[1753-2]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1753&amp;Itemid=986]]></url><city><![CDATA[Kerry]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Fire Prevention Officer for a company with sites in Kilkenny and South East.
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:

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[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[2026-03-04 14:08:15]]></date><referencenumber><![CDATA[1754]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1754&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Project Engineer for a client in Mayo. The Project Engineer is responsible for safely coordinating and leading projects associated withNew Product Introductions, Process Improvements, Automation, Aseptic processing, NewProcessing equipment with some Facility / utilities modifications to incorporate same.
 
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:

Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. Processing equipment would include e.g., Autoclaves, RABS &amp;amp; Isolator Filling machines, LAF units, Compounding skids, Vessels, Containment booths &amp;amp; Stopper processing equipment.
Writing User Requirement Specifications.
Selecting Vendors and completing Vendor evaluation matrix
Writing RCE's, placing orders, Project Management &amp;amp; Design review meetings.
Working to the ASME BPE 2019 Standard and relevant ISPE Guidelines etc.
Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel.
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.
Contribute to a team environment on specific technical problem-solving forums associated with Product manufacture &amp;amp; Aseptic fill.
Deliver on Process improvement / cost reduction projects.
Lead your regular weekly / bi-weekly Project review meetings with your Project team.
Attend the weekly Tier 1 meeting with your manager.
Any other duties as assigned.

 
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. Minimum of 2 to 5 years’ experience.
Project Management experience with a 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.
 Culture fit: Have a people centred approach in a team environment whilst upholding the values and ethos of the company.
Undertake any travel that the role may require for design review meeting, build inspections, Factory Acceptance Tests (FAT’s) etc.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Engineering Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-05 17:27:49]]></date><referencenumber><![CDATA[1755]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1755&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Engineering Technician for a leading manufacturing company in Sligo.
To work as a team member to support Moulding/Tooling, Assembly in line with all safety, regulatory and organizational 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:

Advance performance of site through Key Performance Indicators and metrics.
Partner with Operations to ensure daily production is met.
Responsible to be Subject Matter Expert on routine maintenance of all areas of responsibility regarding equipment and process.
Interface and work with equipment vendors as required for detailed issue resolution.
Embrace and drive the site Maintenance Excellence Programme.
Fabrication of ad hoc mechanical and electrical parts to ensure efficient repairs, upgrades, maintenance.
Participating in project teams and completing assigned projects/tasks.
Providing technical support to operations to ensure production schedule is achieved including optimization of moulding and assembly process.
Providing technical support to operational and strategic projects when required.
Documentation of all activities in line with cGMP requirements.
Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
Execution of routine manufacturing documentation, commissioning and validation protocols on an ongoing basis.
Providing an efficient maintenance service to include Moulds/ Moulding M/C’s, Assembly and Test Equipment.
Perform equipment Calibration per procedural requirements.
Updating the Maintenance and Calibration systems and ensuring compliance.
Interpreting electrical and mechanical drawings for decision making and improvements.
Troubleshooting and resolution of day-to-day technical issues in:
Injection mould machine and tooling – Equipment, Process, Electrical/Mechanical tasks.
Assembly (automatic and semi-automatic)
Equipment, Process, Electrical/Mechanical process, control systems.
Maintaining the overall cGMP of the production areas.
Execution of all work utilizing Maximo management system.
Any other duties as assigned.

 
What you need to apply:

· Leaving Cert OR Sr. Level Trade Certificate OR Technical FETAC 6 from Level 3 institute or commitment to obtain same.
Experience in following technical area:  o Mold Tooling  o Electrical  o Automation
Demonstrated computer skills such as:  o Operating Computer interfaced equipment.
Interfacing with ERP systems.
Minimum of 3 years in a high precision manufacturing industry post qualification
Proven problem-solving ability on complex equipment.
Minimum 2 year of experience in regulated manufacturing environment required.
Requires proven problem-solving skills under the pressure.
The position requires detailed evaluation of a number of viable solutions to each problem.
]]></description><jobtype><![CDATA[Contractor]]></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[Test Infrastructure and Tools Dev Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-13 13:31:53]]></date><referencenumber><![CDATA[1759]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1759&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Test Infrastructure and Tools Dev Engineer for a leading manufacturing company in North Galway
 
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:

Work with tools development and project teams to develop toolchains and test environments for Mechatronic Validation on active R&amp;amp;D projects in local and global sites.
Design and develop automation solutions for optimal test infrastructure development and operational efficiency.
Design and develop test software and scripting in Python, C++, LabVIEW, TestStand or CANoe/CAPL, aligning with standard test software architecture and development processes.
Maintain existing tool development and deployment in active use at local and partner sites.
Review customer and internal test tool requirements.
Create innovative software solutions for real-time testing of ADAS systems.
Develop and deploy system test interfaces (hardware and software).
Develop and deploy automated test sequences, mostly using Python as a base platform.
Develop and deploy mechatronic validation solutions.
Validate test software and test systems for development project operations.
Establish positive communication channels between sites, both internally and externally to ensure effi cient cooperation and collaboration.
Document software design following company Standards.
Participate in code reviews, both as reviewer and reviewee.
Participate in technology / supplier / test tool reviews.
Contribute to continuous improvements in process and test and tool methodologies.
Document own developments, to train and support users in the successful use of the toolchains at internal and external sites.
Any other duties as assigned.

 
 
What you need to apply:

A relevant Technical Engineering Degree e.g. Computer Science, Physics, Electronic Eng. or equivalent.
Minimum 5-years industry experience in high-end automotive or mechatronic technology and test environment development .
Additional industry standard certifications can be advantageous.
A keen eye for detail, coupled with unparalleled problem-solving acumen.
Exceptional communication and collaboration skills, underpinned by the ability to thrive in a fast-paced, team-centric environment.
The ideal candidate will have experience in common coding languages, Python, C++, Java or similar.
The ideal candidate will have experience in industry standard platforms such as TestStand, LabVIEW, CANoe/CAPL, MATLAB or similar systems.
The ideal candidate will have experience in Data Management, including application of GCP, AWS, AI-agents or similar technologies.
Familiar with digital hardware and communications protocols (e.g. I2C, PCIe, SPI, UART).
Digital hardware debug experience.
Understanding of software development lifecycles.
Experience in data analytics, data mining or artifi cial intelligence is an advantage.
Experience in Automotive development and validation is an advantage.
Knowledge of ISO26262/ISO15504/SPICE an advantage.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[System Owner Engineer – Syringe Filling]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-13 13:41:16]]></date><referencenumber><![CDATA[1760]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1760&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a System Owner Engineer – Syringe Filling for a leading pharmaceutical company in South Dublin.
Seeking an experienced System Owner Engineer (SOE) 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.
 
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:

This is a critical role supporting a high-speed, GMP-regulated fill-finish manufacturing environment.
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 company global standards.
Develop and implement: Maintenance strategies, Critical spare parts strategy, Preventive, maintenance programs and 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.
Any other duties as assigned.

 
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: GMP and regulatory expectations Annex 1 Aseptic processing principles 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[Project Engineer (Automation)]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-19 09:49:44]]></date><referencenumber><![CDATA[1761]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1761&amp;Itemid=986]]></url><city><![CDATA[Mayo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Project Engineer (Automation)
Team Horizon is seeking a Project Engineer (Automation) for a client in Mayo. The Project Engineer is responsible for safely coordinating and leading projects associated with Automation, Aseptic processing, new processing equipment, packaging, new Facility builds or modifications/extensions.
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.


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:

Safely coordinate the delivery of processing equipment to the site based on planned timelines and scope.
Processing equipment would include e.g. autoclaves, LAF units, moulds, extruders, packaging equipment, automated vision inspection systems, lyophilsers, isolators, containment booths, stopper processing equipment and equipment upgrades – both hardware and SCADA.
Coordination of equipment installation and services hook up, working with equipment vendors and engineering personnel.
Lead the Project Team or support the Project Manager in Factory Acceptance Testing program.
Coordination of all equipment documentation requirements.
Commissioning of equipment for validation activities.
Preparation of equipment training and maintenance protocols.
Report into the Project Manager on project progress and advice/support on key project outcomes
Contribute in a team environment on specific technical problem solving forums associated with product manufacture, aseptic fill and Packaging.
Deliver Process improvement projects.
Work with the relevant Business Unit team leaders to implement improvement opportunities
Lead regular Equipment/Facility Project review meetings.
Attend the weekly Tier Meetings.
Attend monthly Department Meetings

What you need to apply:

Third level qualification in an Engineering or Science or equivalent discipline/experience (Automation)
Experience of working within either the medical device or bio/pharmaceutical industry would be an advantage but not necessary.
5 years+ relevant years’ experience
Project Management experience is preferable but not necessary
Interpersonal skills required to operate in a multi-function project team set up.
Ability to work within a team and on 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.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></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[Construction Manager - Pharma]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-23 10:25:51]]></date><referencenumber><![CDATA[1764]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1764&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Construction Manager for a leading pharmaceutical company in South Dublin.
Will be supporting a substantial construction projects in the Pharmaceutical Industry. Coordination of construction activities to deliver the projects against Safety, Quality and Schedule commitments.
 
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:

Oversight and planning of construction works in tandem with site contractors, construction managers and facility stakeholders.
Drive safe execution of works.
Ensure timely delivery of construction tasks.
Reporting and management of the construction deliverables.
Participate and run daily whiteboard sessions to plan work
Drive a safety culture through the project team. Ensure that projects are in compliance with site and corporate regulatory authority guidelines.
Work with construction contractors to ensure work is planned in advance, materials available, staff on site and safe and thorough planning is carried out – review and approve RAMS, SPAs etc.
Solution seeking to complex project phasing and execution issues. The Project Engineer will need to work with stakeholders to identify the optimum path forward
Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.
Role model safety leadership. Support a safe working environment by driving compliance with environmental health/safety practice, rules and regulations.
Ensure projects are delivered with superior levels of environmental control, health and safety built in.

 
What you need to apply:

Experience of working in a similar construction environment – large project on a Biopharmaceutical site beneficial.
Knowledge of safety, GMP and environmental regulatory requirements.
Demonstrated strong Communication and Leadership skills.
Demonstrated ability to collaborate with stakeholders to achieve optimal outcomes. Ability to work to tight deadlines in a fast-moving environment
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Construction Project Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-23 10:27:55]]></date><referencenumber><![CDATA[1765]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1765&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Construction Manager for a leading pharmaceutical company in South Dublin.
Will be supporting a substantial construction projects in the Pharmaceutical Industry. Coordination of construction activities to deliver the projects against Safety, Quality and Schedule commitments.
 
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:

Oversight and planning of construction works in tandem with site contractors, construction managers and facility stakeholders.
Drive safe execution of works.
Ensure timely delivery of construction tasks.
Reporting and management of the construction deliverables.
Participate and run daily whiteboard sessions to plan work
Drive a safety culture through the project team. Ensure that projects are in compliance with site and corporate regulatory authority guidelines.
Work with construction contractors to ensure work is planned in advance, materials available, staff on site and safe and thorough planning is carried out – review and approve RAMS, SPAs etc.
Solution seeking to complex project phasing and execution issues. The Project Engineer will need to work with stakeholders to identify the optimum path forward
Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.
Role model safety leadership. Support a safe working environment by driving compliance with environmental health/safety practice, rules and regulations.
Ensure projects are delivered with superior levels of environmental control, health and safety built in.

 
What you need to apply:

Experience of working in a similar construction environment – large project on a Biopharmaceutical site beneficial.
Knowledge of safety, GMP and environmental regulatory requirements.
Demonstrated strong Communication and Leadership skills.
Demonstrated ability to collaborate with stakeholders to achieve optimal outcomes. Ability to work to tight deadlines in a fast-moving environment
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></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[Quality Technician]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-27 13:28:39]]></date><referencenumber><![CDATA[1769]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1769&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Quality Technician for a leading manufacturing company in Sligo.
To 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.
 
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:

Operate within the QC/ IQA and Metrology Areas, as required.
Complete incoming product testing per the relevant approved specifications and procedures.
Complete in-process and final release product testing per 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.
Any other duties as assigned.

 
What you need to apply:

A third level qualification in an appropriate discipline is desirable. 2+ years’ Experience within a regulated GMP environment is desirable.
Technical/Business Knowledge -Job Skills/Experience Required 1 year plus 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[Marketing Associate ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-30 11:24:19]]></date><referencenumber><![CDATA[1770]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1770&amp;Itemid=986]]></url><city><![CDATA[Dublin ]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Marketing Associate
Team Horizon is seeking a Marketing Associate for a client in Dublin. In this vital role you will assist in developing and implementing marketing strategies regarding company's products, delivering value for our client’s customers and the patients we serve
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:

Contribute to product branding, communications, and promotional activities to support brand strategy and execution.
Coordinate effectively with brand, sales, and cross-functional teams to ensure aligned and high-quality delivery.
Define and deliver marketing projects, with guidance from the line manager.
Provide marketing support across a portfolio of products, ensuring consistent execution of key initiatives.
Manage and track cross-functional budgets against plan, proactively identifying and addressing any deviations.
Plan and organise cross-functional Brand Team meetings to enable effective decision-making and alignment.
Support the planning and execution of congresses, ensuring strong presence and seamless delivery.
Act as Responsible Employee for domestic and international sponsored meetings, ensuring compliant and efficient end-to-end logistics.
Coordinate and deliver multichannel activities, including digital and print campaigns, to maximise customer engagement.
Lead materials management, ensuring accuracy, availability, and compliance of all promotional materials.
Develop high-quality promotional materials in partnership with the Brand Lead and line manager, working closely with external agencies and the service centre.
Drive materials through the PromoMats approval process in a timely and compliant manner

What you need to apply:

Degree educated
Experience in managing multiple projects and working under pressure, within a cross-functional team
Experience developing and implementing a wide range of successful digital initiatives across multiple channels
Working experience within a regulated environment (ABPI/IPHA or similar)
Numerical and scientific aptitude: support to interpret data and trends and to understand scientific papers and concepts
Experience with Microsoft Office and familiarity with AI-enabled tools to support productivity and content development
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Commercial]]></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[Clean Utilities Engineer]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-03-31 16:31:55]]></date><referencenumber><![CDATA[1772]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1772&amp;Itemid=986]]></url><city><![CDATA[Dublin]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Clean Utilities Engineer for a leading pharmaceutical company in South Dublin.
Clean Utilities Engineer with previous relevant experience of Pretreatment Systems, Clean Steam, WFI and Process Air generation and distribution systems, to provide client side design input at Detailed Design, Commissioning, Qualification and handover stages of a design project for a Fill/Finish Building. The scope of the role also includes design input and support during the project phases for various ancillary areas such as the existing Warehouse, a new -30Deg Coldroom, Laboratory reconfigurations and general site infrastructure. The position is a hybrid position with an on-site (3 Days) and remote working element.
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:

To support the client side design team in its efforts associated with the expansion project.
To provide technical expertise working with other project stakeholders, in order to achieve design deliverables.
To track, manage and communicate adherence to discipline project milestones.
To coordinate client side clean utilities (Clean Steam / WFI / CA) design by liaising with Site SME’s and Engineering Technical Authority (ETA).
To assist client side design reviews in the area of Clean Utilities for the expansion project.
To participate in cross functional package, area, or overall design teams as required in support of overall design goals and expectations.
To input into Technical Assessment in support of the instrumentation framework, and/or procurement agreements.
To participate in design reviews, model reviews, etc., and to input on technical elements of the design.
To execute Drawing, URS, HDS, SDS, Equipment &amp;amp; Instrument Specifications and other reviews associated with the Clean Utility installations.
To participate in CMSAT’s / Loop checking, including any trouble shooting activities
To provide input and assistance to Automation, C&amp;amp;Q and Validation in terms of equipment packages as required.
To participate in the design reviews and specifications review of any Vendor Package Equipment in the new Facility.
Provide attendance / assistance for FAT’s / SAT / C&amp;amp;Q and Validation activities at various locations, site or Vendor, as required.
To provide input into the calibration program for clean utilities. To coordinate with site Metrology Group to ascertain calibration requirements and to ensure the execution of calibrations, both equipment and field instruments, in line with these requirements.
To liaise with the site Maintenance Group and to ensure that any data gathering required to support the MAXIMO system requirements.
To provide input / direction into schedule and cost discussions, as required, in order to meet the project objectives as defined by the Design Manager, Project Manager and Steering Committee, or designees.
A site presence will be required during construction. This will involve oversight / supervision of the Clean Utilities element of the expansion project.

 
What you need to apply:

Minimum of 5 years of experience in pharmaceutical design / build / commission / start-up with direct responsibility for Engineering Documentation, Project Execution or Facility Design. Direct experience in a similar scale project.
Ability to challenge, defend and present technical aspects of design and commissioning.
Education Degree level qualification in Chemical / Mechanical Engineering, or similar/equivalent.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job><job><title><![CDATA[Senior Process Safety Engineer ]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-01 09:39:09]]></date><referencenumber><![CDATA[1773]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1773&amp;Itemid=986]]></url><city><![CDATA[Sligo]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Senior Process Safety Engineer
Team Horizon is seeking a Senior Process Safety Engineer for a client in Sligo. The Senior Process Safety Engineer will be responsible for the development, implementation, and management of systems and procedures designed to prevent major accidents and incidents. This role also involves maintaining and continuously improving existing frameworks to ensure a robust, compliant, and fit-for-purpose process safety environment. In addition, the position holds responsibility for overseeing emergency response planning and business continuity strategies.
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 the introduction of new products to the site from a process safety perspective.
Safe Process Design and Review. Evaluate and design safety systems, including emergency shutdown systems, pressure relief devices (PRDs), fire protection, and explosion prevention systems.
Develop and further improve Emergency response and preparedness capabilities.
Chair and document process and equipment HAZOP assessments and other process safety related risk assessments and drive follow up actions.
Complete Pre-Start Up Safety Reviews (PSSR) in line with relevant Technical Standards.
Be responsible for process safety elements associated with running product campaign(s) on plant and ensuring that all processes are managed effectively.
Propose, develop, and implement improvements and modifications from a process safety perspective to process areas and equipment to improve operations.
Ensure compliance with relevant legal, site, corporate, and industrial standards.
Interact with the Management of Change (MOC) and change control system and approve from an EHS perspective.
Support safety investigations throughout the site and troubleshoot related process safety issues.
Lead or participate in root cause analysis (RCA) for major incidents.
Review and approve process safety-related documentation, for example, Process Hazard Analysis and Capital Project Lifecycle system requirements.
Provide relevant training and mentor less experienced engineers, supporting their development in process safety.
Conduct safety audits and continuously improve the Site safety management systems.
Engage with internal and external stakeholders, including regulatory authorities and third-party auditors, to drive compliance and continuous improvement.
Utilize digital risk management tools, process safety modeling software, or data analytics for risk assessment and improvement of process safety practices.
Integrate process safety with sustainability and environmental initiatives, such as safe handling of hazardous waste and reducing process-related emissions.
Interact with the Global Process Safety SMEs and maintain Process Safety KPIs and Metrics.
Participate in relevant professional networks and support continuous professional development related to process safety.

What you need to apply:

A bachelor's degree in Chemical, Process, or Mechanical Engineering.
5+ years of relevant experience in a process-related industry (e.g., pharmaceutical, chemical, petrochemical).
Strong knowledge of process safety management (PSM) principles, risk assessment methodologies (PHA, HAZOP, LOPA, etc.), ATEX and COMAH principles (related to explosive atmospheres), and relevant industry standards (e.g., IEC 61508/61511 for functional safety).
Excellent analytical and problem-solving skills, strong written and verbal communication skills, attention to detail, and the ability to work effectively within cross-functional teams.
Chartered Engineer status or TUV Rheinland/equivalent certification in Functional Safety would be an advantage.
Experience with process safety digital tools and modeling software is desirable.
Proven ability to collaborate with diverse teams and stakeholders.
]]></description><jobtype><![CDATA[Permanent]]></jobtype><category><![CDATA[EHS]]></category></job><job><title><![CDATA[Data Collection lead]]></title><publisher>Team Horizon</publisher><publisherurl>http://www.teamhorizon.ie/</publisherurl><company>Team Horizon</company><date><![CDATA[2026-04-09 12:30:02]]></date><referencenumber><![CDATA[1774]]></referencenumber><url><![CDATA[https://www.teamhorizon.ie/index.php?option=com_recmgr&amp;view=job&amp;jid=1774&amp;Itemid=986]]></url><city><![CDATA[Galway]]></city><country><![CDATA[Ireland]]></country><description><![CDATA[Team Horizon is seeking a Data Collection lead for a leading manufacturing company in North Galway.
 
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:

Ensures that the Test Data specified by the System Validation team is collected and delivered to stakeholders in time and with the required quality.
Coordinates Data Collection activities for the project.
Reports to Fleet &amp;amp; Operations team lead.
Statistical test requirement analysis
Data Collection plan contributor and reviewer
Delivers the Data Collection Plan and maintains it
Detailed plan of capturing according to each requirement of Data Collection Catalogue(Country, Route type, Weather conditions, etc.).
Specific route planning updates of needed resources and services
PRE-SOCO and SOCO process.
Provides detailed efforts and costs estimations for all Data Collectionactivities
Manages and executes the Data Collection: 1) Preparation of vehicle transport and registration 2) Services for legal aspect of capturing (e.g. Data Protection,GDPR ) 3) Hiring, Training and managing of driver crews &amp;amp; Shift planning.
Ensures vehicle operations are followed as defined by the System Tools coordinator.
Secures daily progress reporting vs plan. Evaluates current operational performance.
Identifies problems in operations processes and works to resolve them in a timely manner.
Maintains clear and accurate operations documents/procedures within a given project for reference purposes.
Ensures compliance to internal or external rules, regulations and standards for data collection
Any other duties as assigned.

What you need to apply:

Degree: Bachelor’s Degree or Diploma in Computer Science, or a related technical discipline.
Core Experience: Minimum of 2 years in a technical data management or operations role.
Technical Advantage: A background in data scripting (SQL/Python), JIRA, Google Cloud Platform and is a significant advantage.
Project management (Agile, Prince2) is highly regarded, but not essential.
Data Formats: Familiarity with JSON, XML, and CSV structures used in automotive logging and toolchain configurations desirable but not essential.
A self-motivated &quot;demonstrable leader&quot; who thrives in a dynamic, high-pressure R&amp;amp;D environment.
Excellent presentation skills with the ability to articulate technical data status to diverse audiences.
A mindset focused on optimizing processes and a proactive approach to problem-solving..
Confident, energetic team player with the initiative to drive tasks to completion.
A proven track record of maintaining exceptional levels of accuracy managing complex batch datasets, compliance documentation, and high-visibility workflow dashboards.
]]></description><jobtype><![CDATA[Contractor]]></jobtype><category><![CDATA[Engineering]]></category></job></source>
