Regulatory Affairs Specialist

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  "Title": "Regulatory Affairs Specialist",
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          "Code": "NC",
          "Name": "North Carolina"
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  "MatchScore": 1,
  "PostedDate": "2026-05-18T18:20:07.309Z",
  "JobCategoryName": "Charter - Quality Assurance",
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  "BriefDescription": "Plans, organizes and implements strategies and activities required to procure regulatory approval for new and revised product lines.  Coordinates and prepares regulatory submissions, including 510(k) premarket notifications, EU MDR Technical Files and other international registrations.  Ensure compliance to all US, EU and international requirements and company policies and procedures regarding submissions and other requirements for market approval of medical devices.",
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  "RequisitionNumber": "REGUL002528"
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