2 Medical Device Regulatory Affairs Jobs in Dublin
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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 19 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 19 days ago
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