Case Study
Tuesday, March 24
04:00 PM - 04:30 PM
Live in Everett
Less Details
Effective process and analytical control strategies are key to ensuring product quality and compliance throughout the pharmaceutical manufacturing lifecycle. This session covers how integrating risk management, innovation, and a lifecycle approach optimizes control strategies and meets regulatory expectations. Learn how a science-based framework supports continuous improvement and delivers consistent product quality. In this session, you will learn how to:
Experienced pharmaceutical leader with over 15 years in drug development and manufacturing. Currently Director at Bristol Myers Squibb, specializing in Chemistry, Manufacturing, and Controls (CMC) and cross-functional team leadership. Previously held scientific and leadership roles at Sanofi, GSK, Thermo Fisher Scientific, MIT, and Johns Hopkins University. Proven track record driving innovation and operational excellence across the pharma value chain.