Principal RA Associate Devices

What you’d do

Manage regulatory projects for medical devices, guide product teams on U.S. and international requirements, develop FDA submission strategies, and assist in schedule planning. Full-time role in Waltham, MA. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• Bachelor's Degree
• 8+ years submission experience
• Prior 510(k) experience
• Experience with manufacturing, quality, clinical, marketing
• Knowledge of U.S. and international medical device regulations