Mary Marshall Purinton

Mary Marshall Purinton has extensive experience in quality assurance and compliance roles within the pharmaceutical industry. Mary'smost recent position was as the Associate Director of Quality Assurance and Compliance at Fulcrum Therapeutics since November 2022. Prior to that, they worked at Takeda from 2016 to 2022, holding the roles of Senior Manager Clinical Quality Assurance Rare Disease and Senior Manager Quality Assurance Vaccine Business Unit. From 2007 to 2016, they worked at Biogen in various quality assurance positions, including Quality Assurance Senior Associate II and Quality Assurance Associate II. In 2007, they briefly worked as an Interviewee while self-employed. Mary also has experience as a QA Associate II at Acambis from 2004 to 2007 and as a QAL Assoc I and Document Control Clerk I at Amgen in 2003.

Mary Marshall Purinton obtained a Bachelor of Science (BS) degree in Marine Biology from Old Dominion University in the years 1994-1999. Mary then pursued a Master of Science (M.S.) degree in Project Management from Boston University from 2005 to 2008. Later, they undertook a Master of Science (M.S.) degree in Regulatory and Clinical Research Management at Regis College starting in 2012. Currently, their enrollment is on hold for the latter degree. Additionally, Mary has obtained certifications in GDPR and Human Subjects Research in the U.S. from CITI Program in December 2022. Mary also holds certifications as an ASQ Certified Quality Auditor and Six Sigma Green Belt from ASQ.