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.
The Global Ultrasound Regulatory Affairs Lead position in the Management & Operations field is open for applications. We aim to respond to suitable candidates as soon as possible. Full responsibilities and requirements are described in the listing above.