42 Fda Jobs in Dunboyne - page 3
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QC Analyst Recruitment by Aphex Group - Dublin of biopharmaceutical QC or GMP lab experience. Knowledge of GMP/regulatory compliance (FDA/EMA). Experience with analytical techniques (e.g., cell culture, aseptic technique). Strong technical writing (SOPs 40000.0 17 days ago
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AR&D Analytical Chemist New CPL Recruitment - Dublin technical background in chemistry, particularly analytical chemistry. • Ability to work to tight timelines. • Good Troubleshooting skills. • Openness to change, receptive to new ideas. • Knowledge of FDA Negotiable 15 days ago
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QC Materials Technical Lead (Sample Management) Morgan McKinley - Dublin in and support audits, both internal and external (HPRA/FDA etc.) Act as the primary point of contact for audit discussions relating to sample management Build and foster strong relationships within the biologics 60000.0 14 days ago
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CQV QA Specialist Life Science Consultants (LSC) - Dublin deviations, change controls, and CAPAs. Ensure Compliance: Monitor adherence to FDA, EMA, and internal quality procedures. Conduct Risk Assessments: Identify and address risks related to systems and processes 100000.0 15 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 23 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 16 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 19 days ago
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QC Instrumental Specialist CPL Recruitment - Dublin of 3 years’ experience working in the pharmaceutical industry is required. Knowledge of quality control operations. Experience of regulatory agency audits and an understanding of laboratory GMP’s FDA Negotiable 29 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 21 days ago
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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 15 days ago
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