Dr. Schultz has held positions of increasing and diverse responsibilities since joining Johnson & Johnson in 1984. He established a Regulatory Sciences function within the Global Regulatory Affairs, Chem - Pharm organization of the Johnson & Johnson Pharmaceutical Research and Development, L.L.C. in January 2002. Prior to joining Regulatory Affairs, Tom directed the activities of the US-based Pharmaceutical Sciences group for 15 years. During that time he also had the opportunity to lead various compound development teams, serve as Development liaison to the Scripps Research Institute (LaJolla, CA), act as Technical liaison to the OMJ parenteral facility (San German, P.R.) and supervise the areas of Pre-Clinical Formulation and Package Development. Tom received both his B.S. degree in Pharmacy and Ph.D. degree in Pharmaceutics from the Philadelphia College of Pharmacy and Science. He is currently pursuing a Master's degree in Regulatory Affairs/Quality Assurance at Temple University. Dr. Schultz presently serves on the Product Quality Research Institute (PQRI) Specifications Working Group and is a member of the PhRMA Regulatory Affairs Coordinating Committee, CMC section. Tom is a past Chairperson of the Philadelphia Pharmaceutical Forum and Land O' Lakes International Industrial Pharmaceutical Research Conference. He served as co-organizer, as well as on the planning committee, of a number of FDA/AAPS workshops.

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