Global Regulatory Affairs Manager, Medical Devices (Hybrid)

Medline Industries is hiring a Manager Regulatory Affairs in Eagan, MN with a hybrid work model. The role oversees regulatory affairs for Medline product lines, guiding teams to develop and execute strategies for domestic and international approvals of medical devices.

The position requires a Bachelor's degree in Regulatory Affairs or related field and 4+ years of regulatory experience. SAP experience and 510(k)/CE filing know-how are preferred. Up to 15% travel may be required.