Todas as vagas
Sr Regulatory Affairs Specialist International
Bioventus
Amsterdam · PresencialSênior (5–10 anos)Tempo integralPublicada em 8 de jul. de 2026
Sobre a vaga
O que você vai fazer
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.
O que eles procuram
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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