Regulatory Affairs Lead - Medical Devices (Global & Equity)

A medical device company seeks a Regulatory Affairs Specialist in Maple Grove, MN, to lead regulatory submission activities, with a strong emphasis on FDA compliance. The ideal candidate will have over 5 years of experience in Regulatory Affairs, preferably in the medical device industry, and expertise in various submission types. This role offers a competitive compensation package, including career development opportunities. Join a dynamic team committed to advancing healthcare through innovative therapies. J-18808-Ljbffr