[{"id":"303","jobref":"2224","jobtitle":"Recruitment Consultant","jobdesc":"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!
\r\n
\r\nWhy you should apply:<\/strong>
\r\n\r\n\t- \r\n\t\tEvery day is different and you can enjoy supporting a range of roles.<\/li>\r\n\t
- \r\n\t\tThe role is generously compensated, and attracts a competitive base salary.<\/li>\r\n\t
- \r\n\t\tExcellent career progression opportunities.<\/li>\r\n<\/ul>\r\n
\r\nWhat you will <\/strong>be<\/strong>doing:<\/strong>
\r\n\r\n\t- \r\n\t\tWorking with clients and hiring managers looking at current and future recruitment requirements<\/li>\r\n\t
- \r\n\t\tDeveloping sourcing strategies to attract and promote top talent<\/li>\r\n\t
- \r\n\t\tLeading interviews for key partners<\/li>\r\n\t
- \r\n\t\tPartnering with hiring managers on complete recruiting life cycle<\/li>\r\n\t
- \r\n\t\tCommunicating with candidates to ensure efficiency and ongoing brand awareness<\/li>\r\n\t
- \r\n\t\tWorking with clients in identifying the right fit candidates<\/li>\r\n\t
- \r\n\t\tExecuting sourcing strategies for talent pipeline campaigns<\/li>\r\n<\/ul>\r\n
\r\nWhat you need to apply:<\/strong>
\r\n\r\n\t- \r\n\t\tRelevant 3rd<\/sup> level qualification<\/li>\r\n\t
- \r\n\t\t2+ years recruitment experience either in house or with a 3rd party agency<\/li>\r\n\t
- \r\n\t\tPharma industry related experience is preferred<\/li>\r\n\t
- \r\n\t\tBrilliant communications skills<\/li>\r\n\t
- \r\n\t\tCustomer focused attitude<\/li>\r\n\t
- \r\n\t\tAbility to engage with multiple customers<\/li>\r\n\t
- \r\n\t\tRemote working experience<\/li>\r\n\t
- \r\n\t\tGreat relationship building skills<\/li>\r\n<\/ul>\r\n","cname":"Lisa O'Connor","applink":"\/303-recruiter\/hr\/recruitment\/sligo\/job"},{"id":"414","jobref":"2351","jobtitle":"QC BioAnalytical","jobdesc":"If you have experience in cell-based potency bioassays, cell culture, GMP\/GDP Elisawe may have the job for you. We are seeking applications for an experienced QC BioAnalytical Sciences for our client, who are a leading biopharmaceutical company based in Dublin.You will act as a senior associate on the manufacturing site, responsible for leading, coordinating, facilitating, and undertaking activities pertaining to lab operations and compliance, with minimal supervision. And as a role model for other lab colleagues.
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\r\nWhy you should apply:<\/strong>
\r\n\r\n\t- \r\n\t\tThis 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.<\/li>\r\n\t
- \r\n\t\tOur client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.<\/li>\r\n<\/ul>\r\nWhat you will be doing:<\/strong>
\r\n\r\n\t- \r\n\t\tPlanning and delivering complex routine\/ non-routine methods and procedures and a large variety of assays.<\/li>\r\n\t
- \r\n\t\tTaking part in the peer review of analytical data.<\/li>\r\n\t
- \r\n\t\tGiving technical guidance while applying expertise and critical thinking to help to resolve technical issues.<\/li>\r\n\t
- \r\n\t\tLeading the training of staff on technical aspects<\/li>\r\n\t
- \r\n\t\tCreating, updating and implementing procedures that comply with appropriate regulatory requirements.<\/li>\r\n\t
- \r\n\t\tQualification of analytical equipment and related testing functions.<\/li>\r\n\t
- \r\n\t\tTaking part in analytical method transfers<\/li>\r\n\t
- \r\n\t\tFollowing standard operating procedures and registered specifications.<\/li>\r\n\t
- \r\n\t\tMaking sure the laboratory is operated in a safe manner<\/li>\r\n\t
- \r\n\t\tEnsuring ongoing compliance to cGLP and cGMP.<\/li>\r\n\t
- \r\n\t\tCompleting laboratory investigation reports and deviations.<\/li>\r\n\t
- \r\n\t\tTaking part in various report and documentation updates and equipment qualifications.<\/li>\r\n\t
- \r\n\t\tParticipating in regulatory agency inspections as required.<\/li>\r\n\t
- \r\n\t\tPlanning and implement procedures and systems to maximise operating efficiency.<\/li>\r\n<\/ul>\r\n ","cname":"Mary King","applink":"\/414\/job"},{"id":"499","jobref":"2436","jobtitle":"Senior MES Automation Integration Specialist ","jobdesc":"Senior MES Automation <\/strong>Integration<\/strong> Specialist <\/strong>– Team Horizon<\/strong>
\r\nWe are now recruiting a Senior MES Automation Integration Specialist to be part of our team on our client’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.
\r\nWhy you should apply:<\/strong>
\r\n\r\n\t- \r\n\t\tOur client has developed a stand-out culture of innovation, inclusion, and development, and consistently features as a great place to work.<\/li>\r\n\t
- \r\n\t\tThe role is generously compensated and attracts a competitive base salary and highly attractive benefits package.<\/li>\r\n\t
- \r\n\t\tExcellent career progression opportunities.<\/li>\r\n<\/ul>\r\n
\r\nWhat you will <\/strong>be<\/strong>doing:<\/strong>
\r\n\r\n\t- \r\n\t\tResponsible for compliance with applicable Corporate and Divisional Policies and procedures.<\/li>\r\n\t
- \r\n\t\tServe 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.<\/li>\r\n\t
- \r\n\t\tConduct investigation activity\/research and give technical advice to the adoption or integration of new technologies and their business impact.<\/li>\r\n\t
- \r\n\t\tLead in the development of standards and procedures and publish\/communicate findings via IOI’s, presentations, white papers, etc.<\/li>\r\n\t
- \r\n\t\tReview, validate & enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.<\/li>\r\n\t
- \r\n\t\tPartner 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.<\/li>\r\n\t
- \r\n\t\tProvides strategic consultancy support to customers in defining or designing business processes and researching and identifying enabling technologies based on customer requirements.<\/li>\r\n\t
- \r\n\t\tActively seek ways to apply technology to business processes, researching and providing information on technical trends and competitors' practices relevant to the assigned client business.<\/li>\r\n\t
- \r\n\t\tAlly with other IT functional areas to remain apprised of project status, and inform customer management of progress; conversely, keep the IT group's technology and service managers aware of user issues and potential potholes or resolve conflicts.<\/li>\r\n\t
- \r\n\t\tDevelop, 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's operation objectives.<\/li>\r\n\t
- \r\n\t\tAccountable for total project scope, budget, completion within budget constraints and schedules completion date.<\/li>\r\n\t
- \r\n\t\tAccountable for successful and timely completion of all tasks\/projects under direct and matrix control.<\/li>\r\n\t
- \r\n\t\tPost completion audit of project after implementation to verify expected benefits vs. costs, both development and operating.<\/li>\r\n\t
- \r\n\t\tProject success is critical to the continued business success of the corporation.<\/li>\r\n<\/ul>\r\nWhat you need to apply:<\/strong>
\r\n\r\n\t- \r\n\t\tFour-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.<\/li>\r\n\t
- \r\n\t\t5-8 years of combined experience in Process Control System Integration (in addition to equivalent experience listed above, if applicable).<\/li>\r\n\t
- \r\n\t\tExperience with MES\/POMSnet, OSI-PI Historian (or equivalent data historian) or DeltaV and\/or Foxboro Distributed Control System (DCS) (or equivalent DCS systems) preferred.<\/li>\r\n<\/ul>\r\n","cname":null,"applink":"\/499-senior-mes-automation-integration-specialist\/laboratory\/scientific\/sligo\/job"}]