Susan Park

Susan Park is a seasoned professional in biotech product development with over 20 years of experience specializing in CMC regulatory strategy, analytical techniques, and CMO management. They served as a Pharma Technical Regulatory Program Director at Genentech, where they led CMC regulatory efforts for early and late-stage development programs. Prior positions include roles at Tercica and Novartis, focusing on analytical work, quality control, and technology development. Currently, Susan is pursuing a B.S. in Chemical Engineering at Columbia Engineering and a Ph.D. in Biomedical Engineering at Northwestern University.