Karlee Camasso, MS, RAC-Devices, RCC-MDR, is a Principal Regulatory Engineer specializing in the medical device industry with over 10 years of experience in regulatory affairs and compliance. Karlee has held various roles, including Quality and Regulatory Affairs Specialist at Cook MyoSite and Senior Consultant at RQM+, and currently works at Philips. Karlee’s expertise encompasses medical device regulatory affairs, quality system development, and project leadership, supported by a Bachelor’s degree in Biology from Seton Hill University and a Master’s degree in Biotechnology from the University of Maryland University College.
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