169 Fda Jobs - page 10
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QC Chemist Recruitment by Aphex Group - Waterford understanding of cGLP, cGMP, and regulatory expectations (e.g., FDA, EMA). Familiarity with pharmacopoeia methods (e.g., USP, EP, BP). Competence in interpreting analytical results and troubleshooting laboratory 40000.0 15 days ago
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Senior In Vitro Bioassay Analyst New CPL Recruitment - County Mayo /FDA) within the Pharmaceutical, Medical Device, CRO, CMO, CDMO Industry. Please note - applicants need to have a stamp 4 or to have unrestricted full working rights for Ireland #LI-DM1 Negotiable 21 days ago
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Quality Control Officer - Ballina New CPL Recruitment - County Mayo and respond to findings. Requirements Min 2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry Negotiable 21 days ago
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Manufacturing manager Haleon - Republic of Ireland Experience in field or plant operations Experience implementing FDA and GMP regulations Strong people agility and Flexibility Experience leading and developing non-exempt and exempt staff High volume and high 12000.0 13 days ago
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Capital Projects Manager - Medical Device Manufacturing Gertek Project Management - Sligo the design, procurement, installation, and validation of capital equipment and facility modifications. Ensure projects adhere to relevant regulatory requirements (e.g., FDA, ISO 13485) and internal quality 12000.0 15 days ago
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QA Specialist Cregg Group - Galway now! Skills: Quality ISO FDA QMS Quality Management NCR's CAPA Benefits: Mobile phone Paid Holidays Canteen Parking VHI Pension Negotiable 35000.0 16 days ago
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NPI Manufacturing Engineer Sigmar Recruitment - Galway . Recognized Excellence: Located in Galway, the company's technology has been recognized by the FDA and awarded CE Mark in 2021. Inclusive Culture: An inclusive work environment where all employees are valued 16 days ago
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QC Biologics New CPL Recruitment - County Mayo regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry. · Experience in project management is desireable · BSc/M.Sc. in a relevant science discipline (e.g. cell € 45000 22 days ago
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Quality Control Officer New CPL Recruitment - County Mayo 2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry. Experience in project management Negotiable 22 days ago
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Global Head of Regulatory Affairs, Pharmaceuticals The Panel Group - Dublin and challenges in key markets. Provide strategic guidance on regulatory pathways and requirements for diverse international regions (e.g., FDA, EU, Canada, ROW, APAC, LATAM). Oversee the preparation and submission 15 days ago
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