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Job description
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
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Worksite address
san francisco, CA, 94199, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.