medlineEagan, MN
Regulatory Affairs Manager – Medical Devices (Hybrid)
Regulatory Affairs Manager – Medical Devices (Hybrid)
Regulatory Affairs Manager – Medical Devices (Hybrid)
medlineEagan, MN
yesterday
Electromedical and Electrotherapeutic Apparatus ManufacturingSurgical and Medical Instrument ManufacturingSurgical Appliance and Supplies Manufacturing
Apply for this role →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.
Also on the board Same function, level within a rung
Level
Manager
Location
Eagan, MN
Occupation
Regulatory Affairs Managers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing
Posted
yesterday