Global SaMD Regulatory Lead - Submissions & Strategy

A global leader in regulatory affairs based in Chicago is seeking a Senior Regulatory Affairs Specialist. The role focuses on supporting the expansion of Software as a Medical Device (SaMD) portfolio, guiding product teams through compliance, and overseeing major submissions to various regulatory authorities. Applicants should possess extensive experience in regulatory affairs, particularly in the medical device field, and strong project leadership abilities. The position offers competitive compensation with a bonus structure and comprehensive benefits package. #J-18808-Ljbffr