Karlee Camasso, MS, RAC-Devices, RCC-MDR, is a Principal Regulatory Affairs Engineer at Philips with over 10 years of experience in the medical device, biotechnology, and pharmaceutical industries. Specializing in medical device regulatory affairs and compliance, they have developed expertise in quality system management and project leadership. Karlee's prior roles include positions at RQM+ as a Senior Consultant and at Cook MyoSite in quality and regulatory affairs. They earned a Bachelor of Science in Biology from Seton Hill University and a Master's Degree in Biotechnology from the University of Maryland University College.
This person is not in the org chart
This person is not in any teams
This person is not in any offices