Lisa Pray

Lisa Pray has a strong background in regulatory affairs, with experience in multiple companies. Lisa is currently working as the Director of Regulatory Affairs at Candela Medical, starting in August 2021. Prior to that, they held roles at Nonin Medical, Inc. where they were a Senior Manager of Regulatory, Clinical, and Design Assurance from January 2021 to August 2021, and a Regulatory and Clinical Affairs Manager from May 2020 to December 2020. Lisa also gained experience at Merz North America as a Regulatory Affairs Manager from May 2016 to May 2020, and as a Regulatory Affairs Specialist from September 2014 to May 2016. Additionally, they worked as a Senior Human Research Review Analyst at The University of New Mexico Health Sciences Center from November 2013 to September 2014. Lisa's early career included roles at Terumo Cardiovascular Systems, where they were a Regulatory Affairs Specialist from May 2013 to August 2013, a Regulatory Affairs Associate from September 2010 to April 2013, and an Engineering Intern from June 2008 to August 2010.

Lisa Pray holds a Bachelor of Arts (BA) degree from Michigan State University. Lisa pursued their undergraduate education at the James Madison College of Public Affairs. There is no specific information available regarding the start or end year of their education at Michigan State University.