Lisa Riley
About Lisa Riley
Lisa Riley is the Associate Director of Biologics GxP, Sample and Data Management at Bristol Myers Squibb, with over 25 years of experience in the pharmaceutical and healthcare industry.
Current Role at Bristol Myers Squibb
Lisa Riley is currently serving as the Associate Director of Biologics GxP, Sample and Data Management at Bristol Myers Squibb. Based in New Brunswick, New Jersey, she leads initiatives in biologics sample and data management, focusing on compliance with GxP regulations. This role underscores her expertise in Good Practices (GxP) and her strategic approach to data and sample management in the biologics sector.
Previous Roles at Bristol Myers Squibb
Prior to her current position, Lisa Riley has held multiple key roles at Bristol Myers Squibb. She served as Group Leader of ASO-GxP, Sample and Data Management from 2020 to 2021 for 6 months in New Brunswick, NJ. Before that, she was Manager II, ASO, GxP, Sample and Data Management from 2018 to 2020 in Hopewell, NJ, and before that, she was Manager, ASO, GxP Operations, Sample and Data Management from 2016 to 2018. These roles reflect her progressive leadership in managing analytical sciences operations and compliance with GxP standards.
Experience at Teligent, Inc.
Lisa Riley worked at Teligent, Inc. in various capacities, beginning as a Research Chemist from 2010 to 2012. She later advanced to Manager, QC, from 2012 to 2016, and ultimately to Senior Manager, Quality Control in 2016. Across these roles, she honed her skills in quality control, contributing to the company's consistency in delivering high-standard pharmaceutical products.
Background in Quality Control and Research
Lisa Riley has a robust background in quality control and research. She started her career as a Quality Control Chemist at ESI - Baxter from 1995 to 1997 and worked as a Quality Control Technologist at chr hansen from 1997 to 1998. She also held positions at Baxter Healthcare, including as a Research Associate II from 1998 to 2007 and as a Contract Technical Writer from 2008 to 2010. These experiences have solidified her expertise in maintaining quality and technical documentation.
Educational Background
Lisa Riley studied at Rowan University from 1991 to 1995. Her academic training provided a solid foundation for her career in the pharmaceutical and healthcare industry, supporting her subsequent roles in research, quality control, and management.