MedTech Regulatory Affairs Specialist | ISO 13485 & CE

Newton Colmore Consulting Ltd in Cambridgeshire is seeking a Regulatory Affairs Specialist to join a growing MedTech team. You will support QA, regulatory compliance, and submissions across Europe, North America and APAC, helping ensure safe, compliant medical devices.

The ideal candidate has 2–5 years of experience, a bachelor’s degree in engineering or biomedical science, and strong knowledge of ISO 13485 and CE marking.

#J-18808-Ljbffr