Regulatory Affairs Specialist - Medical Devices (Onsite MN)
Experis (Austria)
ManpowerGroup's client in the healthcare sector is seeking a Regulatory Affairs Specialist to join the Regulatory Affairs team in Eagan, Minnesota. This 100% onsite role supports division-level regulatory operations, global product registrations, and labeling changes for medical devices and some drug products. The ideal candidate will have a Bachelor's degree and at least 1 year of regulatory affairs experience in medical devices, with experience in international registrations and strong #J-18808-Ljbffr
Vacancy posted more than 2 months ago
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