Lisa Braddock
About Lisa Braddock
Lisa Braddock is the Director of Quality Systems & Compliance, Product Development Quality at Bristol Myers Squibb in Summit, New Jersey. She has extensive experience in quality systems, compliance, and supply chain analysis within the pharmaceutical industry.
Title
Lisa Braddock serves as the Director of Quality Systems & Compliance, Product Development Quality at Bristol Myers Squibb in Summit, New Jersey, United States.
Current Company
Lisa Braddock is currently working at Bristol Myers Squibb, a global biopharmaceutical company, where she holds the position of Director of Quality Systems & Compliance, Product Development Quality.
Past Experience at Bristol Myers Squibb
Lisa Braddock has a robust history with Bristol Myers Squibb. She served as an Associate Director of Quality Systems, Product Development from 2021 to 2023 and prior to that, as an Associate Director of Global Quality Systems Documentation from 2019 to 2021. Both roles were based in Summit, New Jersey and focused on enhancing product development quality systems.
Experience at Johnson & Johnson
Before her current role, Lisa worked at Johnson & Johnson. Her roles included Site Quality Manager, R&D Sterility Assurance Raritan Services / Manager, Document Control from 2018 to 2019, and Manager of Document Control from 2016 to 2018 in Raritan, NJ. Additionally, she was a Compliance Project Lead, Trade Customization from 2012 to 2016 in Skillman, NJ. These positions emphasized her expertise in sterility assurance and document control.
Education and Expertise
Lisa Braddock holds a Master of Science in Industrial Engineering from NJIT, completed between 2002 and 2005. She also earned a Bachelor of Science in Business Management from Rowan University, where she studied from 1997 to 2001. Her educational background supports her extensive experience in quality systems and compliance within the pharmaceutical industry.