21 Fda Jobs in Galway
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Senior Design Assurance Engineer Life Science Recruitment Ltd - Galway /EEC, Medical Device Directive 2007/47/EC, Medical Device Regulation 2017/745, MDR 2002 (UK), FDA Quality System Regulations 21 CFR 820, FDA GLP Regulation 21 CFR 58, FDA Labelling Regulation 21 CFR 801 75000.0 5 days ago
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Quality Manager Cregg Group - Galway of the investigation and timely closure of CAPA and NCRs External audits: lead the company in regulatory agency quality management system audits including FDA and Notified Body Key Requirements: Bachelor Degree 85000.0 3 days ago
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Principal Manufacturing Engineer (m/f/d) Galway LUMA Vision - Galway . • Experienced in working within ISO 13485/FDA regulated quality systems with understanding and application of risk management methodology. • A proven track record in manufacturing and process development 4 days ago
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Quality Manager Life Science Recruitment Ltd - Galway and evolve the Quality Management System (QMS) in compliance with ISO 13485, FDA 21 CFR 820, and other applicable regulations. Oversee all quality aspects of internal manufacturing operations, including batch 100000.0 10 days ago
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Principal Engineer - R&D Life Science Recruitment Ltd - Galway with FEA and SolidWorks for design and analysis. - Minimum 7 years of experience in mechanical design and product development within medical devices. - Strong knowledge of FDA, GMP, QSR, ISO 13485 standards 90000.0 6 days ago
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Calibration Technician Accpro - Galway . Familiar with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO 10012, and ISO 17025 Familiar with NIST, BIPM, NCSL, ASTM, ASME, or other organizations related to metrology, measurements 44025.67 6 days ago
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Program Manager CTOR Medtronic Vascular Galway UC - Galway . Medical device product development experience and a strong understanding of FDA, ICH and IEC standards Experience across the entire product lifecycle. DRM, DFSS or Six Sigma Green Belt Certified Medtronic 12000.0 2 days ago
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Senior Manufacturing Engineer Life Science Recruitment Ltd - Galway 13485 and FDA processes. Experience with statistical techniques (DOE, Six Sigma). Proficiency with engineering software (e.g., AutoCAD, SolidWorks) For further information please contact James Cassidy 70000.0 6 days ago
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Director of Regulatory Affairs Life Science Recruitment Ltd - Galway , and market expansion activities. Manage all regulatory submissions (CE marking, FDA 510(k)/PMA, and other global submissions) and ensure alignment with commercial and operational timelines. Serve 100000.0 14 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 13 days ago
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