Elizabeth Luna
About Elizabeth Luna
Elizabeth Luna is the Sr Manager of Manufacturing Records and Procedures at Bristol Myers Squibb, with extensive experience in quality assurance and manufacturing in the pharmaceutical industry.
Current Position at Bristol Myers Squibb
Elizabeth Luna is the Sr Manager of Manufacturing Records and Procedures at Bristol Myers Squibb. She is based in Summit, New Jersey, United States. In her role, she is responsible for overseeing the manufacturing records and ensuring compliance with industry standards and procedures.
Previous Role at Catalent Pharma Solutions
Before joining Bristol Myers Squibb, Elizabeth worked at Catalent Pharma Solutions as Sr Manager QA Batch Disposition from 2022 to 2023. Her responsibilities included providing QA batch release oversight across multiple sites to ensure the release of BDS and DP products at Catalent Cell and Gene Therapy.
Career at Pfizer
Elizabeth Luna has an extensive career at Pfizer, holding multiple positions from 2016 to 2022. She started as a Production Supervisor, then transitioned to Quality Engineer, followed by Site Quality Approver. Her responsibilities included writing investigations to determine root causes, creating CAPAs, and acting as a Subject Matter Expert (SME) for facility audits.
Early Career at CSL Behring
Elizabeth's early career includes significant roles at CSL Behring, where she served as Lead Parenteral Supervisor, Process Scientist, and Production Coordinator from 2007 to 2016. She was involved in various operations, including developing procedures for new rotary pasteurizers, performing environmental investigations, and managing filling schedules.
Educational Background
Elizabeth Luna studied at Western New Mexico University, where she earned a Bachelor's degree in Zoology/Animal Biology from 2000 to 2004. Her educational background laid the foundation for her extensive experience in the pharmaceuticals and manufacturing sectors.