Qiao Yun (Chaw) He
About Qiao Yun (Chaw) He
Qiao Yun (Chaw) He is the Analytical Lead in Analytical Strategy & Operations at Bristol-Myers Squibb in New Brunswick, NJ, with extensive experience in pharmaceutical analytical development and GMP environments.
Company
Qiao Yun (Chaw) He currently works at Bristol-Myers Squibb as an Analytical Lead in Analytical Strategy & Operations. The company is located in New Brunswick, NJ, where he contributes to the organization's analytical strategy and operational efficiency.
Title
At Bristol-Myers Squibb, Qiao Yun (Chaw) He holds the position of Analytical Lead in Analytical Strategy & Operations. His role involves leading analytical methodologies and ensuring operational excellence in the pharmaceutical development process.
Education and Expertise
Qiao Yun (Chaw) He has a Doctor of Philosophy (Ph.D.) in Organic Chemistry from The Graduate Center, City University of New York. He earned a Master of Science (MS) in Dye Chemistry with a focus on liquid dye formulation from Donghua University. Additionally, he holds a Bachelor of Science (BS) in Dye and Textile Chemistry and Engineering from Zhejiang Sci-Tech University.
Background
Qiao Yun (Chaw) He has worked in various pharmaceutical companies over the years. He was an Associate Director in Analytical Development at Teva Pharmaceuticals from 2016 to 2018 in Elizabeth, NJ. Before that, he worked at Actavis plc as a Research Manager in Analytical Development from 2008 to 2016. He also served as a Senior Research Scientist/Supervisor in Analytical Development at Alpharma Pharmaceutical Inc. from 2001 to 2008. His career began at Block Drug Company, Inc. as a Senior Scientist from 1996 to 2001 in Jersey City, NJ.
Achievements
Qiao Yun (Chaw) He has extensive experience in API and impurity characterization, which is crucial for the safety and efficacy of pharmaceutical products. He has played a key role in technology transfer processes, ensuring smooth transitions from development to manufacturing. Specializing in setting specifications for pharmaceutical products, Qiao ensures product quality and regulatory compliance. He is also known for meeting aggressive timelines in fast-paced drug development and GMP environments. Additionally, he has significant expertise in GMP release and stability testing, ensuring that pharmaceutical products meet regulatory standards throughout their shelf life.