Global Regulatory Affairs Lead, Medical Devices & IVD
BD
BD is seeking a Staff Regulatory Affairs Specialist in the USA (NJ) to lead regulatory strategies and submissions for PreAnalytiX and Lab Specimen Management products. You will guide cross-functional teams across US, EU, and ROW from development through launches, ensuring compliance and timely approvals. Ideal candidates have strong medical device/IVD regulatory backgrounds, with experience in 510(k), PMA, CE marking, and global registrations. #J-18808-Ljbffr BD
Vacancy posted 1 day ago
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