41 Fda Jobs in Dunboyne - page 4
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QA Validation Claran Consultants Ltd - Dublin strategies Ensure all CQV activities are conducted in compliance with GMP, FDA, EMA, and other applicable regulatory standards. Support the qualification of analytical instruments in accordance with regulatory 16 days ago
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Electronic Engineering Life Science Recruitment Ltd - Dublin . ISO 9001 or ISO 13485) and/or FDA quality system regulation processes according to 21 CFR part 820 and EU MDR. Does this sound like your next career move? For more info forward your application 55000.0 23 days ago
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Regulatory Affairs Officer Ocumetra - Dublin will play a critical role in maintaining and enhancing our Information Security Management System (ISMS) and Quality Management System (QMS) and will take the lead in preparing our FDA submission More than 30 days ago
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CQV Engineer PM Group - Dublin . Responsibilities Field execution of Commissioning, Installation & Operational Qualification (IQ/OQ) Experienced commissioning in grey/black utilities Knowledge of recent regulations (ICH, ASTM, FDA, ISPE) and modern 12000.0 23 days ago
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R&D Formulation Chemist Life Science Recruitment Ltd - Dublin formulation shelf-life. Ensure formulations meet regulatory requirements (FDA, EMA, ICH) and contribute to the preparation of CMC (Chemistry, Manufacturing, and Controls) documentation. Support scale-up 50000.0 16 days ago
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Distribution Centre Manager Catalyx - North Dublin experience in medical device/pharmaceutical environment. Strong knowledge of GMP/GDP/FDA regulatory & Known Consignor, Warehouse housekeeping, Health & Safety. Excellent interpersonal and communication skills More than 30 days ago
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Regulatory Affairs Department Head Helsinn Birex Pharmaceuticals Ltd - Dublin pharmaceutical manufacturing plant, Helsinn Birex Pharmaceuticals Ltd (FDA and IMB approved) which has operated at Damastown Industrial Estate, Mulhuddart, since 1997. HBP develops, manufactures and packages 100000.0 18 days ago
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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 23 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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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 25 days ago
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