167 Fda Jobs - page 3
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Validation Quality Engineer Sanmina - Cork JOB TITLE: Validation Quality Engineer DEPARTMENT: Quality Department REPORTING TO: Validation Quality Lead About Sanmina Fermoy Our Fermoy, Ireland, facility is FDA registered and certified to ISO 12000.0 3 days ago
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Product Development Engineer Medical Devices New CPL Recruitment - Dublin , with a strong understanding of design controls and regulatory requirements (e.g., FDA, ISO 13485). · Hands-on experience in product design, prototyping, and testing, including both hardware and software Negotiable 7 days ago
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NPI Project Manager, Advanced Operations Stryker Ireland - Cork . Has applied knowledge of FDA & International medical device regulations. Ability to lead, motivate, and influence a cross-functional team on moderate complexity projects that do not report directly 12000.0 3 days ago
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Regulatory Affairs Specialist 2 Cook Ireland Ltd - Limerick such as regulatory requirements in accordance with ISO13485, MDD 93/42/EEC, EU Medical Device Regulation 2017/745 and FDA QSP 21CFR Part 820 as required. Knowledge of relevant ISO, Eu, FDA medical device standards 12000.0 13 days ago
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Biologics (Manufacturing) Technical Shift Lead AbbVie FOLLOW - Westport, Mayo matter expert with the QA department to interact with HPRA, FDA and applicable health authorities and internal audits. Qualifications So what will you need to be successful in this role? Education 7 days ago
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Document Control Administrator LGC Limited - Tipperary environment for medical devices Basic knowledge of FDA 21CFR820, ISO13485, IVDD98/79/EC, IVDR EU/2017/746 and international regulatory requirements Excellent communication skills and attention to detail 12000.0 5 days ago
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QC Materials Analyst - 6 months FTC Meiragtx Ireland DAC - Clare manufacturing practices (cGMP) required by the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK and the U.S. Food and Drug Administration (FDA). The 29,000-square foot facility 12000.0 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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