42 Fda Jobs in Swords
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Senior Analytical Chemist CPL Recruitment - Dublin chemistry. • Ability to work to tight timelines in a high-pressured environment. • Good Troubleshooting skills. • Openness to change, receptive to new ideas. • Knowledge of FDA and European GMP requirements Negotiable 22 days ago
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CQV Engineer Formulation New CPL Recruitment - Dublin practices, company policies and EU & FDA regulations. Responsible for ensuring that all non GMP equipment, are tested in compliance with project related standards from a commissioning perspective. Deviation Negotiable 3 days ago
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CQV Equipment Engineer Life Science Consultants (LSC) - Dublin . Responsible for ensuring Utilities are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations. Responsible for ensuring that all non GMP equipment Utilities are tested 100000.0 7 days ago
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CQV Engineer New CPL Recruitment - Dublin documentation/electronic records for equipment and utilities assigned. Responsible for ensuring Utilities are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations Negotiable 7 days ago
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Regional Demand Planner New CPL Recruitment - Dublin (ex-Tableau, Excel) • Understanding and exposure to current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) or other regulatory industries • Basic operational understanding Negotiable 2 days ago
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QC Instrumentation Analyst Cpl Resources - Dublin of laboratory GMPs, FDA regulations, and their application to API manufacturing Ability to prepare for and participate in Regulatory and Customer audits Experience in Equipment Validation and change control 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 11 days ago
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QC Instrumentation Analyst New CPL Recruitment - Dublin of regulatory agency audits and an understanding of laboratory GMP’s FDA regulations and their application to API manufacturing. The successful candidate will be required to prepare for and participate Negotiable 23 days ago
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CQV Engineer Hays Specialist Recruitment Ireland Ltd - Dublin practices, company policies and EU & FDA regulations. Responsible for ensuring that all non-GMP equipment utilities are tested in compliance with project-related standards from a commissioning perspective 100000.0 6 days ago
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Drug Substance Process Scientist New CPL Recruitment - Dublin skills. · Experience of FDA and EU licensing and inspection support is desirable · Knowledge of single use systems and new material introduction Skills: • Demonstrated technical capability and aptitude Negotiable 15 days ago
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