Average salary: €18,253 /yearly
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€14 per hour
...We are looking for GMP Cleaners to join our team in a Pharma setting in Clonmel, Tipperary Working pattern: Sundays, 7:30 - 14:00, 6.5 hours weekly. Main duties and responsibilities Work effectively and adhere to all Site Specific and Apleona Procedures and instructions...SuggestedFor subcontractorFlexible hoursWeekend work€101.5k - €200.4k per annum
...Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director GMP Compliance & Inspections to join our Quality department, supporting our IOPS Manufacturing site in Limerick. In this role, you will...SuggestedWorldwideWorking Monday to Friday- ...ð¶ Maintenance Technician â GMP Manufacturing â Longford â Permanent, 12-hour shifts We're hiring on behalf of a leading multinational medical devices and diagnostics manufacturer with a large, long-established site in Co. Longford. The role: You'll join the...SuggestedPermanent employmentShift workNight shift
- ...Engineering). Process Engineering demonstrated experience. Minimum of 8 years post academic engineering experience in relevant GMP processing design and start-up environment. Demonstrated ability to be a Project Lead Demonstrated ability to be a team player...SuggestedFull timeContract workWorldwide
- JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Join us as а Director, GMP Labs to make an Impact at the Forefront of Innovation. The...SuggestedRemote jobFull timeWork at officeWorking Monday to Friday
- ...reviews to ensure systems meet pre-requisites for IQ commencement. · Ensure all C&Q activities are executed in compliance with GEP (pre-GMP) and GMP standards, maintaining inspection readiness at all stages. · Develop and manage the overall C&Q resource plan, including...Suggested40 hours per weekFull timeContract workWorldwide
€47k - €77k per annum
...implementation of appropriate supporting documentation, SOPs and process work instructions compliant with current Good Manufacturing Practices (GMP) Leading technical improvements under the business’s Continuous Improvement Program (CIP). Transferring and implementing processes...SuggestedFull timeTemporary workFixed term contract- ...activities. Collaborate with cross-functional teams to meet performance targets. Ensure strict adherence to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Support and lead assigned actions for Engineering projects within the maintenance team....SuggestedPermanent employmentShift workNight shiftDay shift
- ...walkdowns and readiness reviews; verify systems are ready for Commissioning commencement. Ensure all activities comply with GEP (pre-GMP) and GMP (qualification) standards throughout. Manage the C&Q resources for applicable systems. Co-ordinate with Emerson...SuggestedFull timeContract workWorldwide
€ 12.87 - 22.73 per hour
...Standards Performing equipment cleaning, preparation and execution as well as completing associated documentation Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks Performing various tests and in-process sampling...SuggestedHourly payWorldwideShift work- ...for developing, executing and maintaining CQV documentation and testing activities to ensure manufacturing equipment and systems meet GMP, regulatory and operational requirements. Your new role Job Function In association with the SDP Area CQV Lead, prepare and execute...SuggestedContract workFor contractors
- ...equipment installations, upgrades, commissioning activities and contractor management. Ensure all maintenance activities comply with GMP, health & safety and company standards. Manage maintenance activities and records through the CMMS system, including labour and...SuggestedFor contractorsShift workNight shiftDay shift
- ...more years of experience required in DeltaV application. ·3 or more years of experience required in site-based Commissioning role in GMP environment. · Proven record of proficiencies associated with commissioning and qualification of complex systems on capital...SuggestedFull time
- ...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 timeShift work
- ...Supervisors and Operators through performance management, training, and team development. Ensure compliance with batch records, SOPs, GMP, and full production traceability, maintaining accurate, audit-ready documentation. Drive quality and food safety performance by...SuggestedPermanent employmentFull time
- ...pharmaceutical and biotechnology facilities. This role offers the opportunity to work with a diverse range of analytical, manufacturing, and GMP-regulated systems while contributing to some of Ireland's most advanced life sciences operations. Key Responsibilities Execute IQ...Full time
€30k per annum
...Biomedical or related discipline. Knowledge of basic Chemistry/Microbiology preferred. Knowledge of Good Manufacturing Practice (GMP)/Good Laboratory Practice (GLP) and Good Documentation Practices (GDP) beneficial. Honesty and integrity; must comply with the quality...Full timeInternshipFlexible hours€48k per annum
...and resolution plans clearly to engineering and production stakeholders. Work in accordance with all applicable quality, safety and GMP requirements. Requirements Level 7 qualification in an engineering or technical discipline. At least five years’ experience as...Permanent employmentFull timeTemporary workImmediate startMonday to ThursdayAfternoon shift- ...facilitating and participating in relevant Continuous Improvement (CI) initiatives. Help achieve quality standards and ensure adherence to GMP through effective management of the Quality Compliance Programme, delivering on agreed product specifications. Facilitate the...Internship
£ 39 - 46 per hour
...requirements. Ensure safety standards are met and safe working practices adhered to. * Ensuring compliance with all Quality, Regulatory, GMP requirements and adherence to all copmpany policies and relevant legislation. * Participate in Risk Management activities as required...Contract work- ...where required. Identify and promptly report any process abnormalities, deviations or quality concerns. Maintain high standards of GMP, hygiene and housekeeping across production areas. Clean production equipment and work areas in accordance with established...Contract work
- ...QA Operations Manager with a Leading Life Sciences company in Sligo . The QA Operations Manager leads day-to-day QA oversight of GMP manufacturing, ensuring products and processes meet regulatory, company and site quality standards. The role supports cross-functional...Permanent employment
€57k - €94k per annum
...skills in MS Excel, Powerpoint & Word. ~ Business acumen with an ability to deliver process improvement objectives ~ Good knowledge of GMP / FDA regulatory requirements, housekeeping, health and safety. ~ Genuine interest in investing in people and facilitates individual...Full timeWorking Monday to FridayAfternoon shift- ...lead role in the validation and compliance of computerised systems, ensuring systems are implemented and maintained in accordance with GMP, GAMP 5, data integrity requirements, and applicable regulatory standards . This is a senior-level position suited to a CSV...Full time
- ...optimization . Familiarity with USP, EP , and analytical validation requirements. Understanding of ICH/CDER guidelines and GMP laboratory environments. Experience with analytical techniques such as MS and XRD is desirable. Excellent problem-solving, organizational...Full timeFixed term contract
- ...initiatives. Qualifications Honours Degree in Biotechnology or Bioanalytical related subject; Minimum 5 years' experience in a GMP biologics laboratory; Minimum 2 years' supervisory or team leadership experience desirable; Demonstrated capability to coordinate...Rotating shift
- ..., or similar industries. Proven experience managing budgets, projects, and cross-functional initiatives. Strong understanding of GMP, regulatory compliance, and quality systems. Preferred Professional engineering accreditation or membership of a recognised engineering...Long term contractFull timeFor contractors
- ...project management and supplier management skills Excellent stakeholder management, negotiation, and communication capabilities GMP and quality systems knowledge Internal grades may vary depending on country. Additional Information AbbVie is an equal opportunity...Full time
- ...new products, methods, technologies, and equipment into QC manufacturing. Ensure engineering activities align with IVD, ISO 13485, GMP, and internal Quality Management Systems. Partner effectively with Operations, Quality, Engineering, Supply Chain, and Finance collaborators...Long term contractFull timeLocal area
€54.2k - €88.4k per annum
...successful completion with minimal supervision. Solid understanding of technology transfer principles and lifecycle management within a GMP-regulated environment. Understanding of computerized system implementation, validation principles, data integrity requirements, and...Worldwide