164 Fda Jobs - page 6
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Project Manager - Utilities Gertek Project Management - Sligo and overall facility operations. Compliance and Standards: Ensure all utility systems comply with GMP, FDA, and EHS regulations. Collaborate with QA and validation teams to meet documentation and qualification 12000.0 14 days ago
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Senior Regulatory Affairs Specialist Stryker Ireland - Cork , Science, or related or MS in Regulatory Science 2+ yrs experience RAC(s) preferred Knowledge / Competencies: General understanding of product development process and design control. Understanding of FDA 12000.0 13 days ago
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CQV Engineer Downstream PM Group - Limerick , ASTM, FDA, ISPE) and modern CQV practices with a focus on downstream activities. Qualifications Educated to degree level in Engineering, or Science related area. Minimum of 3-8 year's plus experience 12000.0 11 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 13 days ago
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Senior Manager Risk and Compliance Fidelity Investments - Dublin, Ireland Job Description: Fidelity in Ireland has three legal entities, FISC Ireland, SAI Ireland and FDA Ireland. There are just under 2,000 associates, working across 2 locations (Dublin & Galway Competitive 7 days ago
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Director, Global Patient Safety Sciences - Oncology Regeneron Ireland DAC - Dublin relationships and mentoring junior safety scientists This role might be for you if can/have: Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations 12000.0 6 days ago
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QC Materials Technical Lead Life Science Consultants (LSC) - Dublin /Preventative Action generation. Participate 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 60000.0 12 days ago
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QC Chemist Recruitment by Aphex Group - Waterford understanding of cGLP, cGMP, and regulatory expectations (e.g., FDA, EMA). Familiarity with pharmacopoeia methods (e.g., USP, EP, BP). Competence in interpreting analytical results and troubleshooting laboratory 40000.0 14 days ago
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Validation Engineer Almac Group - Dundalk, County Louth, IE by the EU and FDA. This involves being a local validation subject matter expert, supporting ongoing projects and initiatives, and occasionally traveling to other business sites, equipment vendor sites Not Disclosed 13 days ago
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Capital Projects Manager - Medical Device Manufacturing Gertek Project Management - Sligo the design, procurement, installation, and validation of capital equipment and facility modifications. Ensure projects adhere to relevant regulatory requirements (e.g., FDA, ISO 13485) and internal quality 12000.0 14 days ago
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