A global medical device organization is seeking a Regulatory Affairs Manager to lead the EU Regulatory Strategy for a new Class III medical device. This pivotal role involves developing the regulatory pathway under MDR 2017/745, integrating with global teams to manage product development and approval. Candidates should have proven experience in EU regulatory affairs for Class III devices and be adept at stakeholder management and project leadership. The position offers significant long-term career progression within a well-resourced international environment based in Maidenhead, with required travel to the Oxford site twice weekly. #J-18808-Ljbffr