Susan Schniepp
Vice President Quality
In managing all operational quality–related issues, Susan Schniepp is responsible for cGMP compliance of OsoBio’s facility, as well as regulatory affairs, filings and records, and validation.
An industry veteran of 30 years, Ms. Schniepp recently served as chairwoman of the Monograph Development–Psychiatrics and Psychoactives Expert Committee for United States Pharmacopeia (USP). She has earned several awards from the Parenteral Drug Association (PDA), including its Distinguished Author Award, Distinguished Service Award and Gordon Personeus Award. As the first woman appointed to Pharmaceutical Technology’s editorial advisory board, Ms. Schniepp writes the magazine’s quarterly column, “Inside Standards.” She holds a bachelor’s of science degree from Northern Illinois University.