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Sr Regulatory Affairs Specialist International
Bioventus
Amsterdam · On-siteSenior (5–10 years)Full-timePosted 8 Jul 2026
About the job
What you'll do
Manage and maintain product registrations across Eastern Europe, MEA, and APAC regions while ensuring compliance with international regulatory requirements. Liaise with US Regulatory and Quality teams to resolve inquiries and facilitate the distribution of medical devices.
What they're looking for
Requires a Bachelor's degree in Life Sciences or Engineering and at least 5 years of experience in Regulatory Affairs, specifically within the medical device industry. Experience with international registrations in non-EU countries and knowledge of implantable devices is highly desired.
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