Average salary: €17,468 /yearly
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- 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
- ...commitment to accuracy and quality to deliver ground breaking innovations. This Senior Shipping Assistant will work on site at our GMP Laboratory facility in Athlone as part of our Lab Support team to provide logistical support to the lab facility as it relates to the...SuggestedFull timeWork at officeWorking Monday to Friday
- ...work. This is a place to make a difference in the world. The Role & What You Will Be Doing The Site Self-Inspection Lead ensures GMP compliance and inspection readiness at the manufacturing site. Key duties include leading self-inspections, conducting facility walk-throughs...SuggestedRemote jobLocal areaWorldwide
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Supervisor Biopharma At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact...SuggestedFull timeWork at officeWorking Monday to Friday
- ...culture of collaboration and development. Oversee cross-functional tech transfer activities ensuring compliance with site procedures and GMP. Troubleshoot and resolve complex manufacturing/technical issues driving data-driven decision making. Identify and implement...SuggestedFull time
- ...Business Storytelling Chemistry Manufacturing and Control (CMC) Compliance Management Developing Others Good Manufacturing Practices (GMP) Inclusive Leadership ISO 9001 Leadership Plant Operations Process Control Process Improvements Quality Standards Quality Systems Documentation...SuggestedFull timeWork at officeLocal areaWorldwide
- ...technologies and seek opportunities for continuous process improvements/improved operational excellence. Ensure QC staff receive appropriate GMP training and maintain compliance and high quality standards Create a safety culture enforce safety measures and ensure QC staff...SuggestedFull timeContract workLocal areaWorldwideShift work
- ...assist in the resolution of concerns commensurate with the risk. Liaise with other Department representatives to promote improvements in GMP and Quality standards Comply with our current Manufacturing Division Quality and EHS Management System requirements as relevant to...SuggestedFull timeContract workWorldwideWorking Monday to FridayShift workNight shift
- ...closed within the agreed timeframe. Assist in the installation of new plant and equipment. Maintain appropriate records in line with GMP requirements. Maintain a high standard of cleanliness GMP & EHS adherence and ensure compliance with the 6S (Sorting Simplify Sweep...SuggestedFull timeContract workFor subcontractorShift work
- ...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 timeContract workTemporary workWorking Monday to FridayFlexible hours
- ...of employee engagement through a highly effective support structure developed and implemented for all engineers. Ensure adherence to GMP and safety procedures. Review and approval of validation documentation. All other duties as assigned. Qualifications...SuggestedFull timeLocal area
- ...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...SuggestedLong term contractPermanent employmentContract workTemporary workNight shiftWeekday work
- ...Practices (cGMP) in the performance of day-to-day activities and all applicable job functions ensuring consideration of the impact on GMP and compliance and decisions made. Accountable for compliance via documentation completion risk assessments closing out corrective actions...SuggestedFull timeHybrid workVisa sponsorshipWork at officeRelocationFlexible hoursShift work
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Scientist III - Pharma At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global...SuggestedRemote jobFull timeRelocationWorking Monday to Friday
€45k - €55k per annum
...work closely with clients, internal engineering teams, and technical staff to design, install, and support specialised equipment used in GMP environments. Duties Support clients on‑site, reviewing requirements and proposing suitable mechanical/containment solutions....SuggestedPermanent employment- ...environment by complying with all pertinent environmental health/safety practice rules and regulations. Ownership of equipment/systems in a GMP regulated manufacturing setting. Monitoring of day-to-day performance of their assigned system. Data trend analysis of all...Full timeContract work
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description When youre part of Thermo Fisher Scientific youll do challenging work and join a team that values performance quality...Full timeWorking Monday to Friday
- ...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. Assume overall responsibility for the successful initiation...Permanent employmentContract workHybrid work
- ...is maintained and inspection-ready in accordance with internal and external cGxP requirements and expectation. Ensure adherence to GMP EU Annex 1 FDA and other applicable regulatory guidelines. Support the cross-function readiness for batch certification ensuring all...Full timeWorldwide
- ...Manufacturing Process Automation experience Preferred Qualifications: ~ Engineering Information Systems Computer and/or Software GMP-regulated industry background with experience leading projects and resources. ~8 years of experience in manufacturing including 5 in...Full timeLocal area
€50k - €55k per annum
...manager to ensure the smooth running of the business. Ensure compliance with Dangerous Goods Transportation requirements Maintaining GMP / Housekeeping at a high level at all times. Managing process and material flows. Skills/Qualifications Required: ~3+ years’...Working Monday to FridayFlexible hoursShift work- ...Business Valuations Chemistry Manufacturing and Control (CMC) Coaching Communication Financial Competence Good Manufacturing Practices (GMP) ISO 9001 Plant Operations Problem Solving Process Control Process Improvements Program Management Quality Management Systems (QMS)...Full timeWork at officeShift work
- ...Certify medicinal product in accordance with requirements of product marketing authorization EU Directive 2001/83/EC & 2001/20/EC and EU GMP Annex 16. Assist in the coordination of the QA operational duties relating to product disposition. Participate in investigations...Full timeFixed term contractWorldwide
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Laboratory Setting Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Job...Full timeWorking Monday to Friday
- ...Qualifications : In this role you will need; ~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 ~ Experience in safe handling of dangerous...Full timeFixed term contractShift work
- ...Ensure the laboratory is operated in a safe and environmentally friendly manner. Ensure ongoing compliance with phase appropriate GMP including compliance within the LMS training system. Ensure high levels of Laboratory housekeeping are maintained including inventory...Full timeShift work
- ...UK and Ireland. Overview of Role: The QA Manager will lead and manage quality assurance activities to ensure compliance with EU GMP regulatory requirements and company standards. This role involves oversight of quality systems batch release processes audits and continuous...Full timeContract workRemote work
- ...control. Support of Commissioning and Qualification activities. Preparation updating and execution of Batch Records SOPs and other GMP documentation. Provide process and equipment related training as required within the Manufacturing Department....Full timeContract workWorldwideFlexible hoursShift work
- ...field with substantial experience. ~5 years of experience as an Automation Engineer within the biotechnology industry in a regulated GMP environment delivering Emerson DeltaV solutions (S88 model) and/or high-level expertise in PLC and SCADA based systems including integration...Full timeRelocation package
- ...Key Responsibilities Responsible for supporting all tasks related to the technology system project lifecycle from solution design to GMP qualification. Project management and execution of assigned projects including project prioritisation resource management status...Full timeLocal area