Global Medical Device Regulatory Lead
Listed on 2026-09-29
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Healthcare
Healthcare Compliance, Medical Device Industry, Medical Science, 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.
This opening is for the Global Medical Device Regulatory Lead role at Aurora Lifesciences.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Medical Device Regulatory Lead role in the description above.
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