Regulatory Affairs Manager (IVD) – Lead EU Submissions

A pioneering life sciences organization in Cambridge is seeking a Regulatory Affairs Manager to lead regulatory strategy and execution throughout the product lifecycle. The role involves managing submissions, overseeing post-market activities, and mentoring junior talent. Candidates should have over 5 years of experience in regulatory affairs, particularly in IVD or medical devices. A competitive salary package and benefits are on offer. #J-18808-Ljbffr