Regulatory Affairs Technical Writer - CERs & Submissions

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.