Global Medical Device Regulatory Lead
Listed on 2026-10-06
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Healthcare
Medical Device Industry, Healthcare Compliance, Medical Science Liaison, Medical Science
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 are currently recruiting a Global Medical Device Regulatory Lead for our team in United Kingdom.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Medical Device Regulatory Lead role in the description above.
We appreciate your interest in this position.
Join Aurora Lifesciences and contribute to our ongoing work.
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