Erin Hoffman

Erin Hoffman possesses extensive experience in regulatory affairs and product management. Currently serving as a Specialist in Regulatory Affairs at CONMED Corporation since September 2022, Erin previously held the position of Regulatory Affairs Coordinator within the same organization. Prior roles include Technical Writer at Invitae, where responsibilities involved project management for document control systems in an in-vitro diagnostic/cGMP environment, and Product Manager at CME America LLC, overseeing product planning and execution across multiple product life cycles. Erin also has a background in quality assurance, serving as QA/RI Lead at CME America LLC and as a Quality Specialist, along with a foundation in customer service. Erin earned a Bachelor's degree in Biology from the University of Colorado Denver from 2014 to 2018.