Global Regulatory Affairs Specialist II — Submissions

A global leader in hearing solutions is seeking a Specialist II in Regulatory Affairs. This role involves preparing global regulatory submissions for product approvals while ensuring compliance with FDA, Canada, and EU regulations. The ideal candidate will have 2-3 years of experience in regulatory affairs at medical device companies and hold a relevant bachelor's degree. The job offers flexibility in a hybrid work environment and several employee benefits, including medical coverage and career growth opportunities. #J-18808-Ljbffr