Elizabeth Brown

Elizabeth Brown is a Principal Scientist at Bristol Myers Squibb, where she has over 20 years of experience in quality and validation within the pharmaceutical industry. Her current role involves managing the Computer System Validation Testing program, ensuring compliance with FDA regulations and overseeing various computer validation projects for new product introductions and internal IT initiatives. She has a strong background in applying quality assurance practices, including writing and reviewing critical documentation such as requirements and design specifications, which are essential for regulatory compliance.1

Before joining Bristol Myers Squibb, Brown held several significant positions, including Senior Manager of Global Quality Computer Compliance at AbbVie and Senior Quality Assurance Engineer at Zelis Healthcare. Her expertise extends to operational excellence, where she utilizes Lean Sigma and Six Sigma methodologies to improve efficiency and reduce costs in validation projects.12

Brown earned her Bachelor’s degree in Communication and Media Studies and Sociology from Rutgers University. Her extensive experience in the pharmaceutical sector includes roles focused on ensuring that systems meet stringent quality standards while also managing risks associated with computer systems in manufacturing environments.1

Overall, Elizabeth Brown is recognized for her leadership in quality assurance and compliance within the pharmaceutical industry, contributing significantly to the operational integrity of Bristol Myers Squibb.