Kim Huynhba
Adjunct Professor, Department of Chemistry, Professional Master Program @Illinois Institute Of Technology
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WORK HISTORY
Adjunct Professor, Department of Chemistry, Professional Master Program @Illinois Institute Of Technology
Chicago, IL, US
Teaching on-line \"GMP\" and \"ICH/FDA Regulations\" courses for the Regulatory Science Certification Program.Taught \"Analytical Chemistry in Pharmaceutical Labs\" for the Master of Professional Science Education Program.
EDUCATION
University of Delaware
Certification, Project Management
Millersville University of Pennsylvania
B.S., Chemistry and Mathematics
Villanova University
M. Sc., Analytical Chemistry with the late Dr. Robert L. Grob
SKILLS
ABOUT KIM HUYNHBA
30 years of experiences in GMP, QMS, QRM, Drug Stability, Analytical Development, Stability, project management in pharmaceutical industry. Provide consulting services for companies, especially small or virtual companies. Subject matter expert (SME) for trials, disputes, litigation cases. Provide training on cGMP for pharmaceutical industry since 2002 globally. Perform 3rd party audit and manage CROs on behalf of clients.ACADEMIC EXPERIENCES:Adjunct Professor at Temple University, School of Pharmacy, in PA; at Illinois Institute of Technology, Chemistry department, Chicago, IL. Teaching GMP, Quality Audit, ICH Quality Guidelines, Regulatory Compliance, and Analytical Validation. BOOKS PUBLISHED:1.\"Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies and Best Practices\", 20082.\"Current Trends of Stability Testing to support Global Markets\", 2010 3.\"Analytical Testing for the Pharmaceutical GMP Laboratory\", 2022VOLUNTEER ACTIVITIES- USP Council of Expert and Chair of USP Small Molecules IV Expert Committee (20••••25 cycle), USP Council of Convention- Member at Large of EAS Board of Director, 20••••22, 2013 President- Chair of 2024 AAPS Career Committee- Steering committee of AAPS CRO, Pharma Impurities and CMC Focus Groups. Founder and Past-Chair of AAPS Stability Focus Group- Chair of USP Good Documentation Practices Expert Panel (2010-15), Member of USP Impurities of Drug Product Expert Panel (2010-present), Member of USP General Chapters Physical Analysis Expert Committee (2010-11), Member of USP Reference Standard Project Team (2009-10), Member of USP Prescription/Non-Prescription Stakeholders (20••••10)- Member of CHPA Impurities Breakout Group (2009-11).
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