9 Medical Device Regulatory Affairs Jobs
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Senior Regulatory Specialist Real - Cork in obtaining and retaining country-specific regulatory registrations worldwide MDSAP Implementation: Manage the implementation of the Medical Device Single Audit Program within the organization Regulatory £60.43 - £64.74/hour 28 days ago
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Clinical Affairs Specialist Wallace Myers International - Galway info see Skills: Clinical Affairs Clinical Trials Medical Device Regulatory affairs 60000.0 3 days ago
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Regulatory Affairs Specialist 2 Cook Ireland Ltd - Limerick Overview The Regulatory Affairs Specialist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices 12000.0 2 days ago
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Sr Regulatory Affairs Specialist I Hollister Incorporated - F26 F3X5 Ballina, MY, IE : Pharmaceutical and Medical Device Act (2014) Australia: Therapeutic Goods (Medical Devices) Regulations 2002 Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Exercise 7 days ago
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Regulatory Scientist 2 Cook Ireland Ltd - Limerick with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets and providing regulatory affairs input for the functional areas. Reporting to: Principal Regulatory 12000.0 3 days ago
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Director of Regulatory Affairs Life Science Recruitment Ltd - Galway Director of Regulatory Affairs Medical Device Start-Up Galway About the Company Our client is an ambitious, well-funded medical device start-up based in Galway, entering a critical phase 100000.0 3 days ago
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Regulatory Affairs Officer Ocumetra - Dublin Engineering, Life Sciences, Quality Management) Minimum 2–4 years of experience in regulatory affairs, preferably with medical device software or digital health products Familiarity with ISO 13485, ISO/IEC More than 30 days ago
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Regulatory Affairs Specialist Cregg Group - Clare in the Medical Devices industry is required. Understanding of applicable guidelines and regulations, for example experience with ISO 10993 Experience with FDA regulatory requirements, European Medical Devices 65000.0 17 days ago
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Computer Systems Validation (CSV) Engineer Catalyx - Cork within regulated industries (pharmaceutical, biotech, medical devices, etc.). Experience with FDA 21 CFR Part 11, GAMP 5, and other regulatory guidelines. Skills: Strong knowledge of validation principles More than 30 days ago
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