WuXi Biologics has over 2,800 employees, including more than 260 overseas returnees and scientists with advanced degrees and work experience abroad. We have rich experience in antibody development, manufacturing, quality control, preclinical research and registration in European and American markets. All members of senior management team have worked at the forefront of the biologics industry with an average of over 20 years of industry experience in their fields of expertise, enabling us create a world-class pharmaceutical biologics discovery, development and manufacturing team.
Chris Chen, Ph.D.
Chief Executive Officer
Nearly 20 years of experience in bioprocess development, scale-up, manufacturing and quality. Formerly CEO of Shanghai Kanda; COO of Shanghai Celgen; Director of Process Science & Production at AME (now Eli Lilly), Manager of BioProcess Technology at Merck. Ph.D. from University of Delaware.
Weichang Zhou, Ph.D.
Chief Technology Officer, Senior Vice President
Over 25 years of biologics development and manufacturing experience. Previously Sr. Director of Commercial Cell Culture Development at Genzyme, Sr. Director of Process Sciences and Engineering at PDL Biopharma, and Associate Director of Fermentation and Cell Culture at Merck. Postdoc at University of Minnesota, DECHEMA and ETH Zurich. Ph.D. from University of Hannover, Germany.
Chiang Syin, Ph.D.
Chief Quality Officer
Over 29 years of experience in U.S. FDA regulatory review and GMP compliance of biological and biotech products including time as Branch Chief in the Office of Compliance and Biologics Quality, the Center for Biologics Evaluation and Research (CBER). Prior to WuXi Biologics, he was a Gates Project International Expert for the Center of Food & Drug Inspection (CFDI) of CFDA. Dr. Syin received his Ph.D. in chemistry from the Catholic University of America and joined the U.S. FDA after his postdoctoral training at NIAID and the NIH.
Jing Li, M.D., Ph.D., MBA
Senior Vice President
Over 20 years of experience in biologics discovery, strong experience in leading mab discovery projects from ideas to early clinical development at Novartis and Wyeth, program team leader for critical mab projects, formerly Assoc. Director at Novartis and Sr. Scientist at Wyeth. M.D., Ph.D. from Peking University and MBA from Yale University.
Wei-Chun (Wesley) Wang, Ph.D.
Over 25 years of process & product development experience in biopharmaceutical industry. Previously Scientific Director, Commercial Analytical Science Team Leader at Amgen, Senior Scientist at Immunex and Senior Research Investigator at Bristol-Myers Squibb. Ph.D. in Biochemistry from University of Georgia.
Gang Huang, Ph.D.
Over 20 years of industry experience in the U.S. including 14 years of biopharmaceutical experience at Amgen as Scientific Director in Process & Product Development. Leading cross-functional process and technology development teams and analytical development of innovative protein products and biosimilars. Ph.D. in analytical chemistry from Purdue.
Paul Liu, Ph.D.
Over 30 years of experience in bioprocess development and GMP manufacturing in U.S. and China. Previously with Merck and Nektar. Most recently was CTO at Livzon Mabpharm and CTO/Co-founder of Shanghai Henlius Biotech. Ph.D. in Chemical Engineering from University of Delaware.
DQ Wang, Ph.D.
Over 25 years of experience in FFF, scale-up, process transfer and production at Bayer Global Biologics. Obtained Ph.D. in Engineering from Oregon State University. Served as Chairman of Industrial Advisory Board for the U.S. National Science Foundation Research Center for Pharmaceutical Processing. Is an adjunct professor at Purdue University and Peking University. Former President of CABS (Chinese American BioPharmaceutical Society) in the US.
Liang Tang, Ph.D.
Nearly 30 years’ experience in protein therapeutic discovery and cell culture manufacturing process development. Formerly with Bayer Pharmaceuticals (USA) and Heska. Obtained Ph.D. degree in protein biochemistry and molecular biology from McGill University, Canada and postdoctoral training, Imperial College of Science, Technology and Medicine, in London, UK.
Over 25 years of experience in process development, technical transfer, clinical manufacturing and process validation at both large pharma and CMO organizations. Formerly with DuPont Pharma, Bristol-Myers Squibb, Johnson & Johnson, and Laureate Biopharma, Inc. Received MS degree in Biochemistry from New Mexico State University.
Jincai (Jimmy) Li, Ph.D.
Over 18 years of experience in process development, technology transfer and scale-up. Formerly with Genentech Inc., Tanox, Inc., and Diversa Corporation (now Verinium), Received Ph.D. degree in Chemical and Biochemical Engineering from University of Maryland Baltimore County.