Regulatory CMC Expert
Suzanne has over 20 years of experience in the pharmaceutical industry. She began her work in Kalamazoo, Michigan at The Upjohn Co., where she remained employed with Pharmacia and Upjohn, Pharmacia Corporation, and Pfizer, Inc. until leaving in 2005 to utilize her regulatory affairs expertise in consulting. After beginning her career in control laboratory operations and analytical methods development at The Upjohn Co., she joined the consumer products group, where she was responsible for analytical methods development, project management, and CMC regulatory strategy and documentation for over-the-counter human health products. She then took a position in the CMC regulatory group at Pharmacia, where she gained considerable experience in animal health regulatory affairs managing projects and preparing CMC documentation for animal health registrations in the US, Europe, and other markets. Her 14 years of experience in regulatory affairs also include human health clinical trial and market applications, management of a global CTD template change control team, and participation in process improvement teams and regulatory affairs infrastructure initiatives.
Suzanne holds a Bachelor of Science in Chemistry degree from the University of Michigan.