44 Fda Jobs in Dublin - page 3
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AR&D Analytical Chemist Cpl Resources - TEG - Dublin , particularly analytical chemistry. Ability to work to tight timelines. Good Troubleshooting skills. Openness to change, receptive to new ideas. Knowledge of FDA and European GMPs requirements, particularly 12 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 12 days ago
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BI Analyst (Digitalisation Project) New CPL Recruitment - Dublin is a distinct advantage. · Experience in life science sector, GMP solutions deployment and validation and FDA's regulations for electronic documentation (FDA 21 CFR Part-11) will be a distinct advantage Negotiable 20 days ago
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Electronic Engineer Life Science Recruitment Ltd - Dublin principles (e.g. 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 55000.0 16 days ago
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Quality Operations Manager Embecta - Dublin Certification is a bonus). Knowledge of FDA requirements and experience managing FDA audits. Experience with process validation, sterilization, and clean room environments is advantageous. Strong interpersonal 12000.0 18 days ago
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Planner New CPL Recruitment - Dublin environment. Experience with ERP systems (e.g., SAP, Oracle, JD Edwards). Familiarity with GMP, FDA, and regulatory requirements in pharma manufacturing. Excellent organizational and time management skills Negotiable 25 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 14 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 19 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 19 days ago
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