Regulatory Affairs Specialist II — Med Devices (Remote)

Sonova Group is looking for a Specialist II in Regulatory Affairs to prepare submissions for clinical investigations and ensure compliance with global regulatory standards. This role involves supporting project teams and coordinating regulatory responses. The ideal candidate will have 2-3 years of experience in regulatory affairs and strong knowledge of FDA and EU regulations. The position is remote, and offers a competitive salary and benefits including medical coverage and a 401(k) plan. #J-18808-Ljbffr Sonova Group