Cure Talent is currently seeking a Principal Regulatory Affairs Specialist to join a global medical device organisation in Oxford. In this role, you will be pivotal in supporting the development and approval of a new medical device programme under MDR 2017/745, ensuring product compliance through all stages.

We are looking for candidates with proven Regulatory Affairs experience, strong knowledge of MDR 2017/745, and an ability to work collaboratively within cross-functional teams. This is a high-profile opportunity to contribute to innovative product launches in a supportive environment.