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Job TitleRegulatory Affairs Specialist Job Description Your role: Develop global regulatory strategies for software medical devices ensuring ongoing compliance throughout the product lifecycle. Prepare and manage regulatory submissions and approvals in the US, Europe, and Canada.
Your mission Alle potentiële sollicitanten worden aangemoedigd om de volledige functieomschrijving door te lezen alvorens te solliciteren. Create and follow up on purchase orders and ensure timely delivery of goods and services. Maintain daily communication with
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