Jennifer Walsh

Maia Pharmaceuticals
Vice President of Quality & Manufacturing Sciences
Jenn is passionate about using data driven analysis to optimize processes to their fullest potential. She has been fortunate enough to apply these skills for over 20 years at top-tier pharmaceutical companies.
Jenn was most recently Director of Robustness & Validation within Bristol-Myers Squibb Global Drug Product Manufacturing Science and Technology organization located in Plainsboro, NJ. She joined BMS in 2006 following similar Science and Technology roles at Schering Plough during their consent decree period and beginning her career at Merck, West Point, PA.
Jenn holds Bachelor Degrees in Engineering & Environmental Science from Drexel University. She is a trained black belt and an active member of ISPE co-chairing the ISPE PQLI Process Validation team. Jenn has recently served as Program Committee Chair for the ISPE 2015 Process Validation Conference and Co-Chair of the 2016 Process Validation Statistics Conference.