Regulatory Affairs Manager – Combination Product (UK, On‑Site)

Cpl Life Sciences is seeking a Regulatory Affairs Manager in West Oxford to lead regulatory activities for a novel combination product. The candidate must have over 5 years of Regulatory Affairs experience, particularly within medical devices and combination products. Responsibilities include developing regulatory strategies, authoring CTD dossiers, and collaborating with cross-functional teams. The role offers full relocation support for candidates living 50+ miles away and includes a competitive salary with a 15% bonus and additional perks such as private healthcare and wellness programs. #J-18808-Ljbffr