Meagan Heurion
About Meagan Heurion
Meagan Heurion is a Senior Research Associate in Process Analytics at Bristol Myers Squibb in Seattle, Washington, with extensive experience in cellular therapy manufacturing and a strong background in the healthcare industry.
Current Role at Bristol Myers Squibb
Meagan Heurion is currently employed as a Senior Research Associate, Process Analytics at Bristol Myers Squibb in Seattle, Washington, United States. In this role, she is involved in process analytics, contributing to the development and optimization of pharmaceutical production processes.
Previous Experience at Fate Therapeutics Inc.
Before her current position, Meagan Heurion worked at Fate Therapeutics Inc. She served as a Clinical Manufacturing Specialist for seven months in 2020, followed by a year-long tenure as Manufacturing Associate II from 2019 to 2020 in San Diego, California. During her time at Fate Therapeutics, Meagan gained valuable experience in clinical manufacturing and cell therapy production.
Career at Juno Therapeutics, Inc.
Meagan Heurion was employed at Juno Therapeutics, Inc. as a Manufacturing Associate II for one year from 2018 to 2019 in Bothell, Washington. Her experience at Juno Therapeutics involved responsibilities related to the manufacturing processes for cell therapies, further enhancing her skills in this specialized field.
Education and Academic Background
Meagan Heurion holds a Bachelor of Science (B.S.) degree in Molecular, Cellular, and Developmental Biology from the University of Washington, where she studied from 2013 to 2015. Prior to this, she earned an Associate of Science (A.S.) degree in General Biology from Whatcom Community College between 2010 and 2013. Her academic background has provided her with a strong foundation in biological sciences.
Expertise in Cellular Therapy Manufacturing
Meagan Heurion has substantial expertise in cellular therapy manufacturing. This expertise encompasses the production of cell-based treatments for various diseases, which is critical in the field of regenerative medicine and immunotherapy. Her skills include Good Laboratory Practice (GLP) and Good Manufacturing Practices (GMP), which are essential for maintaining high-quality standards in laboratory and manufacturing environments, as well as aseptic processing to ensure sterility.