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Medical Device Regulatory Writing Specialist

Job in Southampton, Hampshire County, SO15, England, UK
Listing for: Biocomposites
Full Time position
Listed on 2026-08-04
Job specializations:
  • Research/Development
  • Healthcare
Job Description & How to Apply Below

Biocomposites, based in Keele, UK, is seeking an experienced Regulatory Affairs Specialist (Technical Writing) to lead CER creation and revisions to support regulatory submissions. You will collaborate across R&D, clinical, regulatory, and technical teams to compile robust documentation for EU MDR 2017/745 and FDA Q-submission processes.

The role requires expert literature searches, critical data appraisal, and high-quality technical writing with attention to regulatory guidelines.

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