Global Ultrasound Regulatory Affairs Lead

Mass Digital Health is looking for a Senior Regulatory Affairs Specialist to support Ultrasound product clearances by coordinating regulatory submissions, guiding cross-functional teams, and leading regulatory intelligence initiatives. Candidates should have over 5 years of experience in medical device regulatory affairs, with expertise in 510(k) and EU MDR documentation. This office-based role requires strong communication skills, a Bachelor’s/Master’s Degree in a relevant field, and the ability to work closely with regulatory teams.

A competitive salary range is offered, along with a comprehensive benefits program.
We invite applications for the Global Ultrasound Regulatory Affairs Lead position located in MA, United States. We appreciate your interest in this position. Join Mass Digital Health and contribute to our ongoing work. Take a moment to read everything above and see whether this role is right for you.