CAPT Craig Kiester, RPh, M.S., RAC

Division Director, Division of Regulatory & Business Process Management II, OPRO, OPQ, OGD, CDER

CAPT Craig Kiester is a Division Director in the Office of Product Quality in the Center for Drug Evaluation and Research. He manages the project management staff responsible for co-leading the review of the quality portion of ANDA’s.  Prior to joining the FDA, he worked in home infusion pharmacy.  In 2001 he started his career with the United States Public Health Service when he came to the FDA’s Office of Generic Drugs as a Chemistry Project Manager.  Within the Office of Generic Drugs, he has also held positions as a Regulatory Review officer and a Microbiology Project Manager.  CAPT Kiester received a Bachelor of Science in Pharmacy, in 1998, from Duquesne University and a Master of Science in Health Science from Trident University in 2012.

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