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Eliza Yeung, PhD



Eliza Yeung, Ph.D. has over 16 years’ experience in biopharmaceuticals, Contract Research Laboratory, and Contract Manufacturing Organization. Eliza has expertise in Quality by Design (QbD), Design of Experiments (DOE) using JMP (SAS), and currently leads the Process Characterization (PC) program in R&D Services. Prior to PC position, as R&D Strategic Projects Manager, she developed an open innovation (OI) program which helped focus research efforts in expression technologies, analytics, DOE and QbD, and has led to multiple conference presentations and new service offerings. Prior to Cytovance, Eliza held positions at ARL (OKC), Genzyme, and Novazyme Pharmaceuticals. She has extensive experience in technical project management, regulatory compliance, analytical method development/validation and glycoprotein analysis. Eliza has a B.Sc. in Chemistry from the University of Hong Kong, a Ph.D. in Organic Chemistry from the University of Chicago and completed her postdoctoral training in bioorganic chemistry at the University of Minnesota Twin Cities.

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