Regulatory Affairs Manager – Medical Devices (Hybrid)

Medline Industries, LP in Eagan, MN seeks a Manager Regulatory Affairs to lead regulatory strategy for medical device divisions within a hybrid work model. You will oversee the regulatory affairs team and coordinate domestic and international approvals. The role requires at least 4 years in regulatory affairs for medical devices, RAC certification, and experience with 510(k) and CE files. Travel up to 15% may be required.