Lori Grace

Lori Grace has over 20 years of experience in the medical industry. Lori began their career in 2000 as a Development Scientist at Birch Point Medical (Travanti Pharma). Lori then worked as a QC Manager at PDL Biopharma from 2004 to 2008, followed by a role as a Sr QC Manager at Genmab from 2008 to 2010. In 2010, they began working at Lutonix Inc as a Principal Regulatory Affairs Specialist and Sr. Analytical Lab Manager, and was promoted to Regulatory Affairs Manager in 2016. From 2017 to 2018, they worked as a Regulatory Consultant at River Pines Consulting, LLC. Lori then worked as a Regulatory Program Director at Genentech from 2018 to 2022. Currently, they are employed as a Sr. Director Regulatory Affairs at Reflow Medical.

Lori Grace began their education at UW-River Falls from 1984 to 1986. Lori then went on to the University of Minnesota, where they obtained a B.S. in Chemistry from 1986 to 1988.