Global Regulatory Affairs Specialist III – Medical Devices

A global medical technology company is seeking a Regulatory Affairs Specialist III in Arden Hills, Minnesota. This role involves managing regulatory submissions to the US FDA and EU. Responsibilities include compliance reviews and collaboration on product strategies. The ideal candidate has at least 3 years of experience in regulatory affairs, skilled with submissions for Class I, II, and III medical devices. A hybrid work model is offered, with the expectation of being in the office at least three days a week. #J-18808-Ljbffr