Senior Regulatory Strategist – Medical Devices

Lumicity in San Francisco is seeking a Principal Regulatory Affairs Specialist to own regulatory strategy for a novel medical device platform. You will drive FDA submissions, collaborate with engineering, quality, clinical, and product teams, and guide development from design through commercialization in a fast-paced, early-stage environment.

The role offers significant ownership over regulatory strategy and execution, with direct interaction with the FDA and scalable processes as the portfolio