Medical Device Regulatory Programs Manager

Lumicity, a growing ultrasound medical device company in the San Francisco Bay Area, is seeking a Regulatory Program Manager to drive cross-functional medical device programs from development through regulatory submissions. The ideal candidate will have extensive experience in regulatory program management and a strong understanding of FDA guidelines. This role requires collaboration with multiple teams to ensure timely and organized project deliverables. Responsibilities include preparation for FDA 510(k) submissions and managing documentation readiness for regulatory filings. #J-18808-Ljbffr Lumicity