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IVD Regulatory Specialist — Submissions & IVDR
Job in
Cambridge, Cambridgeshire, CB21, England, UK
Listed on 2026-08-22
Listing for:
Medibeam
Full Time
position Listed on 2026-08-22
Job specializations:
-
Healthcare
Medical Science Liaison
Job Description & How to Apply Below
Medibeam in Cambridge is seeking a Regulatory Affairs Specialist to own regulatory submissions and IVDR/IVDD activities for IVD products. You will prepare regulatory and technical documentation and help manage lifecycle activities across multiple markets.
The role focuses on ensuring ongoing compliance within an ISO 13485 QMS environment, supporting PMS and cross-portfolio regulatory work, and driving process improvements to enhance efficiency. This is a site-based position in Cambridge.
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