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
- ..., repair, validation support, and continuous improvement activities are delivered safely, efficiently, and in compliance with quality, GMP, and H&S requirements. Key Responsibilities Toolroom Operations Plan, coordinate, and prioritize Toolroom activities (repairs,...SuggestedPermanent employment
- ...literacy with proficiency in MS Office (Outlook Word Excel Powerpoint). Minimum of 3 years of related experience in a pharmaceutical GMP or EU regulated environment is required. PHYSICAL REQUIREMENTS Ability to lift /move up to 50 pounds. Ability to sit or...SuggestedFull timeDay shift
- ...team. Roles & Responsibilities Support the design configuration testing and commissioning of Emerson DeltaV DCS systems for GMP manufacturing sites Configure and maintain DeltaV control modules equipment modules phases and batch recipes in line with ISA-88...SuggestedFull time
- ...methodology , protocol and product specifications, Standard Operating Procedures (SOPs) acceptance criteria, and Good Manufacturing Practices (GMP). Reviews data entered into databases and reports and monitors the quality of the laboratory data. This is the perfect job for...SuggestedRemote jobFull timeWork at officeRelocationWorking Monday to Friday
- ...Competencies Experience working in a QC function in a greenfield context of similar size and scale is ideal. Expertise in the release of GMP materials and participant in QC activities such as method transfer validation etc. Experience in Biopharma analysis is desirable....SuggestedFull timeContract workFixed term contractWorldwideFlexible hoursShift work
- ...Assess and define QMS requirements to optimize structure and ensure alignment with business needs and NPD requirements. Support GMP and GDP compliance within the Innovation Excellence organization. Contribute to the development, maintenance, and improvement of QMS...SuggestedPermanent employmentFull timeHybrid work
- ...manufacturing environment. Strong working knowledge of CMMS/EAM systems IoT technologies and data analytics tools. Experience in GMP-regulated environments and familiarity with compliance requirements. Proven ability to lead cross-functional projects and drive adoption...SuggestedLong term contractFull timeRelocation packageRemote workFlexible hours
- ...inspection in accordance with established procedures. Responsible for the writing updating and execution of Batch Records SOPs and other GMP Documentation. Complete detailed batch record and GMP documentation entries which are accurate attributable complete legible &...SuggestedFull timeContract workWorldwideShift workRotating shift
- ...bring their commitment to accuracy and quality to deliver groundbreaking innovations. We have an opportunity within our Analytical GMP labs facility and analytical testing on drug substances and products. This role is based at our site in Athlone, Ireland. Discover...SuggestedRemote jobFull timeWork at officeWorking Monday to Friday
- ...positions related to process development project management engineering/process support and manufacturing ~ Must have strong knowledge of GMP Manufacturing Supply Chain Validation Engineering CMC technical development and pharmaceutical regulations ~ Must have demonstrated...SuggestedFull time
€41.6k per annum
...oriented individual. It would be advantageous to have (but not essential)* 2-3 years working within a QC department in a Pharmaceutical or GMP facility * Experience in Microbiological techniques. At Wallace Myers International Recruitment Agency we specialise in...SuggestedHourly payContract workImmediate startFlexible hoursShift workNight shift- ...recruiting a Micro Analyst to join our site in Ballytivnan Sligo. The Micro Analyst is required to perform microbiological testing within GMP and GLP standards in our global pharmaceutical company. A snapshot of your key responsibilities as a Micro Analyst would be:...SuggestedFull time
- ...follow documented procedures and maintain accurate records. Familiarity with regulatory standards and good manufacturing practices (GMP). Excellent organizational and communication skills. Proficiency in working with laboratory equipment and conducting calibrations...SuggestedPermanent employment
- ...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
- ...all aspects of the Companys Health Safety and Environmental procedures. Ensure all activities are carried out in accordance with the GMP requirements. Education & Experience: NFQ Level 6 Higher certificate qualification in STEM Automation Systems or or...Permanent employmentFull timeWorldwide
- ...relevant documentation is prepared and updated in line with all Quality and Regulatory guidelines and promotes full compliance to all GMP & E&AS requirements. Keep abreast of all relevant technological advancements. Maintain and develop the teams technical and trouble...Permanent employmentFull timeContract work
- ...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...Full time
€45k - €55k per annum
...Working with the general manager, transport manager and purchasing manager to ensure the smooth running of the business. Maintaining GMP / Housekeeping at a high level at all times. Managing process and material flows. Skills Required: Experience within a...Flexible hoursShift workAfternoon shift- ...manufacturing environment. Proven leadership in cross-functional roles including QA Engineering and MSAT. Strong knowledge of Annex 1 GMP and global regulatory requirements. Experience in inspection readiness Excellent communication governance and stakeholder...Long term contractFull timeLocal area
- ...systems (DCS/PLC/SCADA). Participate in troubleshooting data flow issues, interface errors and performance concerns. Contribute to GMP documentation including configuration records, change control and validation support (IQ/OQ). Collaborate with cross-functional...Hourly payLong term contractContract workLocal areaWorldwideFlexible hours
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Join Us as an Associate Research Scientist Make an Impact at the Forefront of Innovation We have successfully supported...Full timeWorking Monday to Friday
- ...Clear communicator with a proactive safety-first mindset Desirable Skills Experience working in regulated environments (GMP cleanrooms healthcare) Additional trade certifications (e.g. refrigeration plumbing) Familiarity with industry safety standards (HSE...Full timeFor subcontractor
- ...plays a key role in supporting a high-volume secondary packaging facility. This position is responsible for developing and maintaining GMP-compliant packaging documentation and driving initiatives that enhance compliance continuous improvement and operational efficiency....Full time
- ...detail and adherence to regulatory standards. ~ Ability to work independently and collaboratively within teams. ~ Familiarity with GMP utility systems (WFI, clean steam, pharmaceutical gases) desirable. ~ Good interpersonal and communication skills. ~ Experience participating...Permanent employment
- ...The PLC Automation Engineer will support the design development commissioning and lifecycle management of automated systems within a GMP-regulated pharmaceutical manufacturing environment. The role involves hands-on PLC programming system integration troubleshooting and collaboration...Full time
€48k - €72k per annum
...inexperienced team members as required. Adhere to all relevant site wide procedures and practices for Safety & GMP Key Skills & Experience ~ Minimum NFQ Level 8 qualification in Science Engineering or relevant discipline ~3 years...Full timeTemporary workFlexible hours- ...Preferred Skills: Agile Manufacturing Assembly Operations Compliance Management Consulting Developing Others Good Manufacturing Practices (GMP) Inclusive Leadership Leadership Manufacturing Processes Manufacturing Science and Technology (MSAT) Manufacturing Standards...Full timeFlexible hours
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Cold Room/Freezers -22degreesF...Full timeWorking Monday to FridayShift work
- ...release site were in the process of introducing a new preparation and filling suite. Essential Responsibilities Ensure compliance with GMP GE Healthcare Corporate Standards Quality Management System (QMS) site policies/procedures regulatory requirements and industry...Full timeRelocation packageWorldwide