Global Medical Device Regulatory Lead

Aurora Lifesciences is seeking a Regulatory Manager to guide regulatory submissions and approvals for class IIa devices across EU, UK, US and other markets. You will lead regulatory strategy, manage Technical Files, and ensure compliance across product development and post-market activities.

The role requires 5+ years in medical device regulatory affairs, strong documentation skills, and experience with EU MDR transitions, US FDA guidance, and cross-functional teams.