42 Fda Jobs in Dublin - page 4
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Subject Matter Expert (SME) - Chemical API PM Group - Dublin to process facility design and construction is essential. Good appreciation of appropriate Regulatory framework, such as FDA, EMA, ICH Guidelines Find out more about PM Group and our projects. Why PM Group 12000.0 20 days ago
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Tech Transfer Lead PE Global - Dublin and procedures, including safety and training. Ensure that the site meets the quality requirements of its customers and applicable regulations (FDA, EU & international standards) with a full understanding of CMC 22 days ago
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Drug Product Process Scientist New CPL Recruitment - Dublin of technical transfers preferable. · Demonstrated aptitude for technical learning and problem solving. · Good communication skills. · Experience of FDA and EU licensing desirable. Skills Negotiable 28 days ago
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Contract Development & Mfg Sr Mgr Amgen - Dublin field Preferred Qualifications: 8+ years of experience in protein, API, DS, DP, or packaging manufacturing environment 8+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory 12000.0 25 days ago
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Senior Project Engineer Embecta - Dublin Experience with ISO requirements and GMP guidelines, FDA regulations, medical device design control, and manufacturing scale up processes Regular embecta is an Equal Opportunity/Affirmative Action Employer 12000.0 27 days ago
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Drug Substance Process Scientist New CPL Recruitment - Dublin background in mammalian cell culture, protein purification or validation. · Good communication skills. · Experience of FDA and EU licensing and inspection support is desirable · Knowledge Negotiable 28 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 29 days ago
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Senior CQV Engineer Commissioning Agents Inc (CAI) - Dublin employees worldwide. We provide commissioning, qualification, validation, start-up, project management, and consulting services related to operational readiness in FDA regulated and other mission-critical 80000.0 28 days ago
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Sr. Engineer, Design Assurance, Risk Management, Human Factors Engineering Emergent Biosolutions - Dublin, IE . • Provide peer review and technical inputs on the key regulatory submission documents, e.g., NDA, FDA Type C, EMA scientific advisory. • Provide support to technical team during regulatory and notified body More than 30 days ago
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Director, Regulatory Labeling Regeneron Ireland DAC - Dublin completion of complex labeling projects. Expert knowledge of FDA, EMA, and international labeling regulations, ICH guidelines, and CIOMS core labeling guidelines. Ability to assimilate clinical and scientific 12000.0 28 days ago
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