|School: Schaefer School of Engineering & Science|
B.S. in Pharmacy from Long Island Univ., M.S. in Pharmaceutical Chemistry from Rutgers Univ., and Ph.D. in Pharmaceutics from Univ. of Connecticut. Dr. Nash is a consultant to the U.S. Food and Drug Administration on cGMP and validation matters
Phamarceutical Manufacturing Program
(Validation & Regulatory Affairs) Before joining Stevens Institute of Technology, Dr. Nash taught at NJIT and St John's University. Dr. Nash spent 24 years in the US pharmaceutical industry as Director of Pharmaceutical Development at Purdue Frederick Co., Manager of Pharmaceutical Product Development at Lederle Laboratories, and Research Associate at Merck. He has over 70 publications, nine US patents, and was co-editor of the book Pharmaceutical Process Validation, published by Marcel Dekker, now in its third edition.
Honors & Awards
Dr. Nash is a recipient of the Lunsford-Richardson Prize in Pharmacy
He is a member of the editorial advisory boards of Journal Validation Technology and Pharmaceutical Formulation & Quality.