Kelsey Lee

Kelsey Lee has a strong background in regulatory affairs, with experience spanning multiple companies. Kelsey is currently the Director of Regulatory Affairs at Delfi Diagnostics, a position they have held since April 2022. Prior to that, they worked at Invitae as the Director of Regulatory Affairs from February 2021 to April 2022. Kelsey also held the role of Associate Director of Regulatory Affairs from October 2020 to February 2021 at Invitae. Before joining Invitae, Kelsey worked at ArcherDX, Inc. as an Associate Director of Regulatory Affairs from August 2020 to October 2020. Kelsey also served as the Sr Regulatory Affairs Manager from January 2020 to August 2020 at ArcherDX, Inc. Prior to that, they worked at Medtronic as a Sr Regulatory Affairs Manager from July 2019 to December 2019. Kelsey also held the position of Regulatory Affairs Manager from April 2016 to July 2019 at Medtronic, and as a Principal Regulatory Affairs Specialist from January 2015 to April 2016. Before their time at Medtronic, Kelsey worked at Covidien as a Regulatory Affairs Product Manager from August 2013 to January 2015 and as a Senior Regulatory Affairs Specialist from May 2011 to August 2013. Kelsey started their career at Wright Medical Technology as a Regulatory Affairs Specialist II from June 2009 to May 2011 and at DePuy Orthopaedics as a Product Development Co-op - Trauma & Extremities from January 2007 to August 2008.

Kelsey Lee pursued their education from 2005 to 2009 at The University of Akron, earning a Bachelor of Science (B.S.) degree in Biomedical Engineering. In terms of additional certifications, they obtained a Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS) in April 2023.