Global SaMD Regulatory Affairs Specialist — Cambridge Onsite

A regulatory solutions provider is seeking a Regulatory Affairs Specialist in Cambridge to support innovative software-driven respiratory devices. You will manage regulatory applications across multiple international markets and ensure compliance throughout the product lifecycle. Ideal candidates should have a Bachelor’s in STEM, regulatory affairs experience, and proven success with FDA submissions. The position requires in-person work at least three days a week, with potential for visa sponsorship after probation.#J-18808-Ljbffr…