Global Regulatory Affairs Specialist - Medical Devices
Experis Technology Group
Experis Technology Group is partnering with a global healthcare organization to recruit a Regulatory Affairs Specialist for an onsite, 12-month contract in Eagan, MN. You will contribute to regulatory affairs efforts supporting global product registrations and labeling changes for medical devices and some drug products. Ideal candidates hold a bachelor’s degree in a technical field, have at least 1 year in regulatory affairs for medical devices, and can support international registrations. #J-18808-Ljbffr Experis Technology Group
Vacancy posted 4 days ago
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