Global Medical Device Regulatory Lead
Resourcing Life Science
A leading life sciences company based in Wisconsin is seeking an experienced regulatory affairs specialist. The role involves managing submission timelines for medical devices globally, authoring technical documentation, and ensuring compliance with international regulations. The ideal candidate has at least 5 years of relevant experience and fluency in English. This position offers the opportunity to contribute to impactful product registrations and collaboration across teams. #J-18808-Ljbffr
Vacancy posted 3 days ago
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