Average salary: €18,244 /yearly
More statsGet new jobs by email
€17 per hour
...We are looking for Part Time GMP Cleaners to join our team in a Pharma setting in Sligo Working pattern:Saturday 08:00 -18:00 Main duties and responsibilities Work effectively and adhere to all Site Specific and Apleona Procedures and instructions Take responsibility...SuggestedPermanent employmentPart timeFor subcontractorFlexible hours€60k - €75k per annum
...EHS Manager - GMP We are currently recruiting an experienced EHS Manager to oversee Environmental, Health & Safety performance on a key client site in Cork. This is a highly client-facing position, where you will work closely with stakeholders on-site, acting as a trusted...SuggestedFull timeFor contractors€54k - €55k per annum
...investigations. Respond to breakdowns, conduct root‑cause analysis and implement preventative solutions. Uphold strong safety and GMP standards at all times. Criteria ~ Fully qualified Electrician with strong maintenance knowledge. ~ Mechanical experience is...SuggestedPermanent employmentFull timeWorking Monday to FridayNight shiftAfternoon shift- ...methods and skills such as auditing, investigation, review, risk management, aseptic processing etc. ~ Building a strong foundation in GMP-regulated environments. ~ Developing applied scientific knowledge through CLS’ proprietary training programmes. ~ Growing...SuggestedPermanent employmentFull timeContract workWork placementInternship
- ...Technical functions to influence strategic decision-making and deliver cross-functional business objectives. Ensuring full compliance with GMP, EHS, and regulatory requirements, maintaining a constant state of audit and inspection readiness across engineering operations....SuggestedLong term contract
- ...currently seeking an experienced Process Engineer with strong upstream and downstream bioprocessing experience to support complex GMP manufacturing projects within a leading biopharmaceutical environment. This role is heavily focused on bioreactor systems, upstream...Suggested40 hours per weekFull timeContract workWorldwide
- ...pharmaceutical machinery and equipment at customer sites worldwide. A key focus of this role is the professional execution and documentation of GMP‑compliant qualification and calibration activities. Your role in our team Independent execution of installation, commissioning,...SuggestedLong term contractPermanent employmentImmediate startWorldwideHome officeFlexible hours
- ...Responsible for installation, maintenance, troubleshooting, and optimization of biologics manufacturing equipment in a GMP-regulated environment. Supports equipment reliability, process improvements, validation activities, and operational efficiency initiatives. Key Responsibilities...SuggestedFixed term contract
- ...initiatives across engineering, cost efficiency, and operational effectiveness. Ensure full compliance with health & safety, quality, and GMP standards within all maintenance activities. Undertake additional duties as required in line with business requirements....SuggestedPermanent employmentFull timeContract workFor contractorsImmediate start
- ...or outsource those services to us here at CLS. The Role As a Microbiology Analyst at CLS, you will play a key role in supporting GMP-regulated manufacturing environments through routine microbiological testing and laboratory support activities. Working as part of the...SuggestedContract workFlexible hours
- ...implement training curriculums and team training plans. Participates in the selection and hiring of Production Operators Maintains GMP / 6S at a high level within the department through the involvement of all team members. Lead / participate in continuous improvement...SuggestedFull timeDay shiftAfternoon shift
- ...substance development and manufacturing Demonstrated experience leading technology transfer, scale-up, and validation of API processes to GMP manufacturing sites for late-stage and commercial programs Strong experience managing CDMOs, including vendor selection, technical...SuggestedWork at officeFlexible hours
- ...inventory requirements. Support new product introduction and provide technical input. Conduct QC testing and maintain compliance with GMP and regulatory standards. Strictly adhere to ISO 9001, ISO 13485, and IMB/FDA requirements. Collaborate with cross-functional...SuggestedLong term contractFull timeLocal areaWorldwide
- ...signed off appropriately. Complete all required documentation accurately, clearly, and completely in line with specific procedures and GMP & GDP standards. Train on multiple steps and rotate between tasks as required/directed. Integrate into the production team,...SuggestedMonday to Thursday
- ...operations team, you’ll carry out multi-stage Active Pharmaceutical Ingredient (API) manufacturing processes in compliance with AstraZeneca, GMP & SHE standards. In addition, you will also: Provide operational expertise at accommodation meetings such as processing risk...SuggestedPermanent employmentFull timeShift work
- ...detail, organisational skills, and ability to manage multiple projects. ~Excellent verbal and written communication skills. ~Knowledge of GMP, HACCP, and food safety standards; BRC knowledge is preferred. ~Flexible approach to working hours to support production and trial...Long term contractPermanent employmentFull timeInterim roleFlexible hours
- ...efficiency targets. ~Drive continuous improvement initiatives to maximise yield, reduce waste and improve OEE. ~Ensure compliance with HACCP, GMP, Health & Safety and customer quality standards. ~Work closely with Planning, Engineering, Maintenance and Quality teams to optimise...Long term contractPermanent employmentFull timeInterim role
- ...addition, the contractor will contribute to day‑to‑day automation support to ensure system stability, availability, and compliance within a GMP environment. This role aligns with the site’s strategic focus on system availability, recovery readiness, and cyber security...Contract workFor contractors
€70k - €80k per annum
...include complex structural builds, cleanroom environments, high-spec mechanical and electrical installations, and strict compliance with GMP (Good Manufacturing Practice) standards. This is a fast-paced, technically demanding project requiring strong coordination across...Full timeFor contractorsFor subcontractor- ...Strong technical knowledge of mechanical, electrical, pneumatic, and process systems; PLC/SCADA fault-finding desirable. ~ Knowledge of GMP, HACCP, PSSR, DSEAR, ATEX, Machinery Directive, and relevant Irish/EU EHS legislation. ~ Project management experience delivering...Permanent employmentFull timeFor contractors
- JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Join Us as a Research Scientist – Make an Impact at the Forefront of Innovation We have...Remote jobFull timeWork at officeWorking Monday to Friday
- JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Join us as a Scientist III (Senior Scientist) At Thermo Fisher Scientific, you’ll discover...Remote jobFull timeWork at officeWorking Monday to Friday
£ 51.79 - 58.7 per hour
...continuous improvement, collaboration and open communication. Compliance & Safety Ensure all activities are carried out in compliance with GMP, GDP and EHS requirements. Maintain engineering documentation in line with site procedures. Support the manufacture of quality...Contract workFor contractorsWork at officeFlexible hours- ...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. QUALIFICATIONS B.S...Full timeHybrid work
- ...and budgets. ~ Ensure compliance with relevant regulations, codes, and standards (e.g., health, safety, environmental, quality, ISO, GMP, LEED). ~ Conduct and document regular facility audits and inspections. ~ Monitor and promote energy efficiency and environmental sustainability...Full timeWork at office
- ...team based regulated manufacturing environment, and ideally 5+ years’ experience at a senior / management level. Good knowledge of GMP / FDA regulatory requirements and current Health and Safety Regulations legislation. Proven track record delivering manufacturing performance...Full timeContract workFlexible hours
- ...River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to...Contract workLocal areaWorldwideFlexible hours
- ...actioned. Stay current with legislation, guidelines and other expectations of the pharmaceutical industry especially in relation to GMP, Quality Management and QP responsibilities including ensuring reports are also engaging in their development and knowledge of changes...Contract workHybrid workRemote work2 days week
- ...procedures, and policies. Qualifications ~3rd level qualification, preferably in Engineering or Science related fields OR 2+ years in a GMP regulated environment. ~ Experience of operating in a highly automated environment. ~ Good I.T. skills are required....Full timeFixed term contractShift workNight shiftAfternoon shift1 day week
- ...biologics, vaccines, protein therapeutics, or related large molecule products ~ Understanding of quality control laboratory operations and GMP requirements ~ Ability to influence and collaborate across cross-functional and international teams ~ Strong scientific...Hybrid workWork at officeFlexible hours