Joan C. Kwong, MS Pfizer Inc.

Joan Kwong has nearly 20 years of industry experience supporting the development of large molecule products, including the past 11 years developing CMC regulatory strategies and global regulatory submissions across the product lifecycle for biosimilars, monoclonal antibodies, and vaccines. Joan joined Pfizer Inc. in 2004 and is currently a Senior Manager within the Global Regulatory Affairs biosimilar team, most recently leading the preparation of drug product dossier content for global license applications from initial submission through approval. She began her career in the pharmaceutical industry in cell culture and purification manufacturing process development for live virus vaccines at Merck and monoclonal antibodies at Pfizer, including manufacture of clinical supplies and start-up of a new commercial manufacturing facility.

Joan obtained her BSE in chemical engineering at Princeton University and her MS in quality assurance/regulatory affairs from Temple University.