Diane Marks
About Diane Marks
Diane Marks serves as the Director of Regulatory Affairs at Adaptimmune, a position she has held since 2019. She has extensive experience in regulatory affairs, having worked in various roles at Teva Pharmaceuticals and Adaptimmune over the years.
Current Role at Adaptimmune
Diane Marks currently holds the position of Director of Regulatory Affairs at Adaptimmune. She has been in this role since 2019, contributing to the company's regulatory strategies and compliance efforts in Philadelphia, Pennsylvania. Her responsibilities include overseeing regulatory submissions and ensuring adherence to industry standards.
Previous Experience at Teva Pharmaceuticals
Diane Marks has extensive experience at Teva Pharmaceuticals, where she worked in various roles from 2002 to 2015. Her positions included Quality Control Associate, Quality Assurance Auditor, Manager of Global Regulatory Affairs, and Senior Manager of Global Regulatory Affairs. This experience provided her with a strong foundation in regulatory affairs and quality assurance within the pharmaceutical industry.
Education and Expertise
Diane Marks earned her Bachelor of Science (B.S.) in Biology/Biological Sciences from Temple University, completing her studies from 1999 to 2002. She furthered her education by obtaining a Master of Business Administration (MBA) from DeSales University. Her educational background supports her expertise in regulatory affairs and business management.
Career Progression in Regulatory Affairs
Diane Marks has progressed through various roles in regulatory affairs over her career. She served as Associate Director of Regulatory Affairs at Adaptimmune from 2015 to 2018. Prior to that, she held multiple positions at Teva Pharmaceuticals, including a five-year tenure in Regulatory Affairs for Generic Drugs. Her career reflects a commitment to regulatory compliance and quality assurance.