Wei Wu

Wei Wu

Associate Director @ Bristol Myers Squibb

About Wei Wu

Wei Wu is an Associate Director at Bristol-Myers Squibb with over 19 years of experience, specializing in the analytical development and biophysical characterization of biotherapeutics.

Current Role at Bristol-Myers Squibb

Wei Wu holds the title of Associate Director at Bristol-Myers Squibb. In his role, he leads analytical project teams, overseeing Contract Manufacturing Organizations (CMOs) and Contract Research Organizations (CROs). His responsibilities include the analytical development of various biotherapeutics and biopharmaceuticals.

Educational Background

Wei Wu completed his Ph.D. in Chemistry from Michigan State University, where he studied from 1998 to 2004. Prior to that, he earned a Bachelor of Engineering in Biotechnology from Shanghai Jiao Tong University, studying from 1993 to 1997. His educational foundation has contributed significantly to his expertise in biopharmaceutical development.

Professional Experience

Wei Wu has amassed over 19 years of experience at Bristol-Myers Squibb. Throughout his tenure, he has developed extensive expertise in the analytical development of monoclonal antibodies, fusion proteins, antibody-drug conjugates (ADCs), and PEGylated proteins. He specializes in protein purification, characterization, and uses advanced techniques such as mass spectrometry.

Technical Skills and Expertise

Wei Wu is skilled in the biophysical characterization of monoclonal antibodies, fusion proteins, and PEGylated proteins. He is also proficient in Laboratory Information Management Systems (LIMS) and has a strong background in regulatory filings, specifically in Chemistry, Manufacturing, and Controls (CMC). Additionally, he excels in technology transfer and troubleshooting for biotherapeutics.

Biologics Development Insight

Wei Wu has a comprehensive understanding of biologics development, spanning preclinical, clinical, and commercial stages. His knowledge covers the full spectrum of biotherapeutics development, providing valuable insights into regulatory requirements and best practices for successful product development and commercialization.

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