Global Medical Device Regulatory Lead
Listed on 2026-10-24
-
Healthcare
Medical Device Industry, Healthcare Compliance, Medical Science Liaison
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.
We would love to welcome a new Global Medical Device Regulatory Lead to our group in United Kingdom.
We are currently recruiting a Global Medical Device Regulatory Lead for our team in United Kingdom.
This is a great opportunity to take on the Global Medical Device Regulatory Lead role at Aurora Lifesciences.
As a Global Medical Device Regulatory Lead, you will play an important part at Aurora Lifesciences in United Kingdom.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).