Lydia B. is an experienced professional in regulatory affairs within the medical device industry, having served as a Regulatory Affairs Manager at CONMED Corporation from 2021 to 2025. Prior to that, they held roles including QA/RA Lead and QA/RA Specialist. Lydia has also worked as a Regulatory Affairs Coordinator at Biom'up, developing compliance strategies for absorbable medical devices, and as an intern in regulatory affairs at Stryker France. They hold a Master’s degree in Engineering for Health and Medicine from Université Claude Bernard Lyon 1, where they were the top of their class.
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