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Medline Industries

Global Regulatory Affairs Manager, Medical Devices (Hybrid)

eagan, MN

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About this opportunity

Medline Industries lists this Global Regulatory Affairs Manager, Medical Devices (Hybrid) opportunity in eagan, Minnesota. Review the employer’s description below for duties, qualifications and application requirements.

Job description

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.

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