10 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 14 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 3 days ago
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Senior Microbiologist CareerWise Recruitment - Cork validations, biocompatibility assessments, and sterility supplier documentation. REQUIREMENTS: * 6+ years experience in Quality or Regulatory Affairs within the medical device industry. *Minimum Microbiology 127185.27 7 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 17 days ago
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Regulatory Affairs Specialist 2 Cook Medical - 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 18 days ago
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Regulatory Scientist 2 Cook Medical - Limerick medical devices. In addition, the Regulatory Affairs Specialist will perform activities associated with PMS, including Post Market Clinical Follow-Up (PMCF), and Clinical Evaluation Plans and Reports (CEPs 12000.0 21 days ago
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Program Manager CPL Recruitment - Dublin standards within the medical device industry. Reporting to: VP of Global Operations Key responsibilities · Program Management: Lead and manage multiple programs that span the lifecycle of medical Negotiable 17 days ago
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Regulatory Affairs Department Lead New CPL Recruitment - Edinburgh The role is a full-time, permanent position working 37.5 hours per week. An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department Negotiable 20 days ago
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Regulatory Scientist 2 Cook Medical - 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 29 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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