Average salary: €18,253 /yearly
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- ...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
€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€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- JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning,...SuggestedRemote jobFull timeWork at officeRelocationWorking Monday to Friday
- ...leadership experience with experience managing direct reports. ~5+ years’ experience in process chemistry or process engineering within a GMP pharmaceutical environment. ~3–5+ years’ experience supporting start-ups and/or new product introductions in pharmaceutical...SuggestedFull time
- ...Commissioning Engineer will provide technical leadership for the commissioning, qualification, validation, and startup of DeltaV systems within a GMP-regulated pharmaceutical manufacturing environment. The position involves supporting equipment installation and operational...SuggestedFull timeContract work
- ...management at a global level. Experience in pharmaceutical, biotech, medical device, or life sciences industries. Working knowledge of GMP, GDP, FDA/EMA regulations, and audit requirements. Experience with ERP systems such as SAP, Oracle, NetSuite, or similar. Prior...SuggestedFull timeContract workFor contractorsLocal area
- ...engagement and collaboration among teams and stakeholders Cross-functional Collaboration Work closely with stakeholders to ensure GMP food safety and quality goals and standards are met. Collaborate with NPD on technical specifications and provide food safety and...SuggestedFull time
- ...with unit operations such as filtration and chromatography. Ensure compliance with Quality Management Systems (QMS) such as ISO or GMP, and adhere to safety protocols in the laboratory. Collaborate with R&D, quality assurance, and manufacturing teams to align on goals...SuggestedTemporary workLocal area
- ...Familiarity with major DCS and working knowledge of BMS/SCADA/PLC systems. Strong customer service, coordination, and interpersonal skills. Good knowledge of GMP regulations. Ability to work across regions, time zones, and travel domestically and internationally....SuggestedWorldwide
- ...CAPA, Quality Assurance, or Quality Engineering. Medical device industry experience preferred. Knowledge of FDA 21 CFR Part 820, GMP, and ISO 13485:2016. Key Skills Strong analytical, investigation, and problem-solving capabilities. Experience leading cross-...SuggestedTemporary work
€ 14.55 - 37.18 per hour
...scheduled, corrective, and post-maintenance calibrations of process and utility instrumentation in accordance with approved procedures and GMP requirements. Performing loop checks, I/O verification, functional testing, commissioning activities, and return-to-service...SuggestedHourly payWorldwideShift work- ...aptitude for decision making and the ability to delegate responsibility appropriately Ensuring adherence to Good Manufacturing Practices (GMP) throughout all areas of responsibility Ensures compliance to Company Health, Quality, Safety and Environment policy Liaise with...SuggestedWork at officeLocal areaFlexible hours
- ...scientific qualification at third‑level in a science or data‑analytics discipline. You will have regulated‑environment experience with GMP exposure strongly preferred. You will have change‑control expertise and be comfortable managing associated quality workflows. You...SuggestedFull timePart timeWorking Monday to Friday
€85k per annum
...all client reporting requirements Qualifications and experience A minimum of five years' experience working in a similar role GMP regulated environment or Facilities Management experience Managing projects in a regulated environment preferred M&E Project...SuggestedPermanent employmentContract workFor subcontractorWorking Monday to Friday- ...chemicals), wholesale distribution facilities (WDA) and supply chain, brokers of medicinal products, laboratory facilities and compliance with GMP and GDP. CE marking and advice on the requirements of MDR and IVDR for all actors within the medical device supply chain. Market...Full timeTraineeshipHybrid work
- ...transfers Qualifications ~ Masters in Chemistry, Biochemistry, Chemical Engineering, or related field ~7+ years’ experience in a GMP biologics manufacturing environment. ~ Experience of Technical Transfers/NPIs is essential. ~ Proven leadership experience with the...Full time
- ...standards. Identify opportunities for quality and service improvement; contribute to continuous improvement projects. Adhere to GMP guidelines and internal quality standards; ensure all activities are documented and traceable. Participate in Root Cause Analysis and...Permanent employmentFull timeContract workTemporary workWorldwideFlexible hoursRotating shiftWeekend work
- JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description Join Us as а Senior Manager, Clinical Lab Scientist - Make an Impact at the Forefront...Remote jobFull timeWork at officeWorking Monday to Friday
- ...Coordinate local shift activities, identify priorities, organise work teams effectively and maintain clear communication between shifts. GMP, Quality and Documentation Complete all tasks in accordance with approved SOPs, batch records and cGMP requirements, ensuring strong...Permanent employmentFull timeContract workWork at officeLocal areaFlexible hoursShift work
- ...marketing authorisation. Ensure manufacture has been carried out in accordance with all applicable Good Manufacturing Practice, e.g., EU GMP Annex 1 and FDA regulations. Ensure the principal manufacturing and testing processes have been appropriately validated; account has...Full time
- ...standards. The Senior Product QA Manager is responsible for compliance with marketing authorisations, current Good Manufacturing Practices (GMP), and supporting New Product Introductions (NPIs). Responsibilities: Manage QP , Regulatory, Change Management and New Product...Full time
- ...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 timeContract workFixed term contractShift workNight shiftRotating shift
- ...Significant experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements. Third level qualification (degree in science or related discipline) or appropriate relevant experience...Full timeFixed term contractHybrid workRemote workWork from homeWorldwide
€ 60 - 75 per hour
...equipment and associated single-use systems as part of a major site expansion in Dublin. 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...Hourly payFull timeContract workHybrid workWork at office- JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Scientist III - Pharma At Thermo Fisher Scientific, you’ll discover meaningful work...Remote jobFull timeRelocationWorking Monday to Friday
- ...responsible for: Working within a manufacturing environment. Filling, packing, labelling. Adhere to good manufacturing practices (GMP). Follow standard operational procedures (SOPs). Perform all duties assigned by your manager. Requirements ~ A Leaving...Contract workTemporary workNight shiftWeekend work
€ 27 - 30 per hour
...vendor service reports, ensuring accurate upload to CMMS platforms and timely closure of associated work orders. Ensure adherence to GMP, cleanroom protocols, PPE requirements, and all pharmaceutical regulatory and safety standards. What You Bring Third-level...Hourly payContract workFor contractors- ..., X and YouTube. Job Description Perform manual assembly and inspection of commodities and components to final product and GMP specifications. Operate semi-automated manufacturing equipment to produce finished product. Perform and document in-process quality...Full timeContract workWorking Monday to FridayAfternoon shift
€ 16.42 - 25.59 per hour
...with troubleshooting in case of equipment failure Performing manufacturing level maintenance on equipment Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks Performing equipment cleaning, preparation and execution...Hourly payShift work