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Regulatory Affairs Technical Writer — CERs & Submissions
Job in
Keele, Newcastle-under-Lyme, Staffordshire, ST5, England, UK
Listed on 2026-02-28
Listing for:
Biocomposites
Full Time
position Listed on 2026-02-28
Job specializations:
-
Healthcare
Medical Science Liaison, Healthcare Compliance
Job Description & How to Apply Below
A leading international medical devices company in Keele is seeking a Regulatory Affairs Specialist. This role focuses on creating and revising clinical evaluation reports (CER) to support regulatory submissions. The ideal candidate should have at least 5 years of medical writing experience, particularly with clinical evaluations and regulatory submissions, and a degree in a life science. The company offers a competitive salary and benefits including a pension and employee discounts.
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