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Mary Joan Hampson-Carlin has over 30 years of experience in the pharmaceutical industry in Quality Assurance and Manufacturing. She has broad responsibility for Laureate’s Quality programs including Quality Assurance, Quality Control, Regulatory Affairs, Validation and Microbiology Laboratory operations. Ms Hampson-Carlin’s experience spans solid dosage manufacturing, sterile products, facility design, validation, manufacturing, Quality Assurance and Research/Clinical Quality Assurance. Prior to joining Laureate in 2000, she worked at Bayer (Miles) in West Haven, Connecticut for 17 years, Schein Pharmaceutical, and Algos. Ms. Hampson-Carlin is currently serving her second five-year elected term as a member of the USP Parenteral Products-Industry Expert Committee.
She is currently co-chairperson of the Expert Committee. She also is a member of the USP Advisory Panel on Controlled Release Parenteral Dosage Forms. Ms. Hampson-Carlin is a graduate of Quinnipiac College with a B.A in Microbiology and holds an M.B.A from the University of New Haven. | 