Average salary: €17,312 /yearly
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- ...audit clients and other stakeholders with respect to supplier/external audits; Perform and maintain all required training and annual GMP training within required timelines; Perform required lead auditor or support auditor activities as applicable for assigned audits;...SuggestedPermanent employmentLocal areaRemote work
- ...with facilities in Dublin and require an experienced Programme Manager to lead automation and control system upgrade projects on their GMP pharmaceutical site. Initial focus is on Siemens PLC/HMI lifecycle upgrades and associated OT/IT integration, reporting into the site...SuggestedContract work
Nicholas Howard Ltd
Dublin2 days ago - ...We are looking for a GMP Specialist to join Apleona team for pharma environment in Dublin Working pattern: Monday to Friday from 08:30-17:00 Job Description: Provide consultancy, coaching, and expertise to internal site teams Lead and support optimisation projects...SuggestedPermanent employmentWorking Monday to Friday
- ...management services across Ireland. We offer flexibility, career progression and a competitive start rate. We are currently looking for a GMP Project Lead to join our team in Dublin Working Pattern : Monday to Friday, from 8:30 to 17:00 Main duties and...SuggestedPermanent employmentFor subcontractorWorking Monday to Friday
- Within this role you will be responsible for the implementation of data governance (DG) standards, policies and procedures into business operations. You will be a site expert on Data Governance, supporting the Regeneron IOPS Data Governance and Integrity program. In this...SuggestedLocal area
- ...assessment and deviation investigation Change control and CAPA management Data Integrity and Good Documentation Practice (GDP) Knowledge of GMP FDA EMA HPRA regulations Validation Master Plan (VMP) preparation and execution Audit readiness and regulatory inspection support...SuggestedFull time
- ...Culture within the PCO. This ensures that all products whether physically or financially managed by the PCO comply fully with applicable GDP/GMP requirements. The SOQ Specialist is responsible for operating within and supporting all aspects of the SOQ Quality Management...SuggestedFull timeHybrid workRelocation packageWork at officeLocal areaFlexible hours
- ...disposition process. Ensure all data ready in timely fashion in support of Opu disposition metric. Perform all duties in accordance with GMP requirements SOPs and controlled documents. Will be flexible to take on additional tasks and responsibilities at the discretion of...SuggestedFull timeContract workWorldwideFlexible hours
- ...consistent treatment of all employees by upholding policies and procedures. • Implement and uphold the Quality System ISO 13485, ensuring GMP compliance, product quality and adherence to safety and regulatory standards ISO 14001. • Ability to drive technical and operational...SuggestedFull time
- ...responsibilities include: To ensure that manufacturing activities at assigned CMOs are appropriately managed in accordance with EU GMP under directive 2003/94/EC and in compliance with EudraLex Vol. 4 Annex 16 and EudraLex Vol. 4 Annex 13, the Rules and Guidance for...SuggestedPermanent employmentContract workPart timeLocal areaOverseas2 days week
- ...you will need: ~3rd level qualification in a relevant discipline ~ Minimum 2 years in a similar role ~ Previous experience in a GMP environment (pharma would be an advantage) ~ Excellent computer skills MS office skills essential Additional Information : AbbVie...SuggestedFull time
- ...Lead commissioning qualification and validation activities for packaging and combination product assembly lines ensuring compliance with GMP data integrity and regulatory expectations. Support project teams by developing and executing validation protocols managing...SuggestedFull timeTemporary workWorldwide
- ...will include quality control testing analytical method transfers new product introductions and technical investigations to support our GMP operations Specific Job Responsibilities Proficiently execute Bioassay techniques such as ELISA Receptor Binding and Cell-based...SuggestedFull timeFor contractorsLocal area
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Scientist II Microbiology At PPD part of Thermo Fisher Scientific youll discover meaningful work that makes...SuggestedFull timeWorking Monday to Friday
- ...components. Team coordination to maximize the effectiveness of all the team members. Documentation of all activities in line with GMP requirements. Cross training within the team and training of new members. Participation in continuous improvement programs to...SuggestedFull time
- ...as rostered and in accordance with Aseptic Unit Standard Operating Procedures (SOPs). Work in line with Good Manufacturing Practice (GMP) requirements and Aseptic Unit SOPs. Carry out quality control and validation activities in line with GMP as described in the...Permanent employmentFull timeContract workTemporary workFor contractorsWork at officeLocal areaWeekend work
- ...safety and compliance leading all emergency procedures and safety systems on shift. Ensure plant and equipment operate to the highest GMP site and corporate standards. Drive completion of all safety and compliance activities including 5S and housekeeping audits....Full timeRelocation packageShift work
- ...process related problems. Contribute to equipment and plant design to ensure that the equipment is fit for purpose meets user safety and GMP requirements and minimizes life cycle cost. Ensures handover of capital project equipment in accordance with the project lifecycle...Full timeFor contractorsRelocation packageFlexible hours
- ...operational readiness. This is a high-impact position where youll collaborate with cross-functional teams shape quality strategies and drive GMP standards from concept to execution. If youre passionate about delivering robust validated systems in a regulated environment and want...Full timeFor subcontractorRelocation package
- ...analytical and problem-solving skills. Qualifications Degree in Environmental Chemical or Safety Engineering or related field. Professional EHS certification (e.g. NEBOSH IOSH PSM ATEX) preferred. Experience in GMP-regulated environments advantageous....Full timeContract workFixed term contract
- ...Conduct MSA studies for new products and new processes. Provide training for manufacturing team members. Ensure adherence to GMP and safety procedures. Review and approval of validation documentation. All other duties as assigned. What you need: B.S...Permanent employmentFull timeContract workHybrid work
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Job Description When youre part of Thermo Fisher Scientific youll do challenging work and join a team that values...Full timeWork at officeWorking Monday to Friday
- ...required to attend meetings at Vendor premises or other sites as required. Desired: ~ Experience commissioning DeltaV systems in GMP manufacturing facilities. Required Skills: BS in Engineering Computer Science or other technical degree. Training completed in...Full timeContract workLocal areaWorldwide
- ...the team Qualifications : Education and Experience You will have: Understanding of the requirements to work in a regulated GMP industry with knowledge of biologics/pharma operations Access to global Trackwise QMS and understanding of the system is preferred...Full timeContract workShift workDay shift
- ...platforms Rockwell PharmaSuite is preferred or other life sciences compatible MES solutions ~ Excellent working knowledge of FDA and GMP guidelines and of software Development Life Cycle (SDLC) and support methodologies required ~ Ability to work in a team-oriented collaborative...Full timeFlexible hours
- ...in Ireland. Youll maintain and improve facility infrastructure while ensuring compliance with pharmaceutical industry standards and GMP requirements. Key Responsibilities ~ Perform carpentry installations repairs and maintenance in pharmaceutical manufacturing environment...Full timeFor contractorsShift work
- ...regulatory and organisational requirements when delegated responsibility. Co-ordination between shift teams to ensure excellence in GMP/ safety and manufacturing activities Point of Contact for Warehousing issues which arise and if escalation to Supervisor is required...Full timeShift work
- ...with manual handling tasks Desirable Background in food production, packaging or pharmaceutical environments Knowledge of HACCP, GMP, or similar hygiene frameworks If you’re reliable, hands-on and committed to excellent hygiene standards, we’d love to hear from you...Night shift
- ...to join a newly created Vaccines company in Ireland . This role offers the opportunity to act as a QA subject matter expert across GMP and other GxP standards, driving supplier oversight, audits, and risk-based quality management. With deep knowledge of international...Permanent employmentContract work
- ...Strong report writing, documentation skills, and attention to detail. Knowledge of regulatory requirements, quality standards, and GMP practices. Experience with validation and qualification (IQ, OQ, PQ) of equipment and processes. For more information and a confidential...Permanent employment
