Sutro Biopharma
Zhimin Xie is a seasoned professional in the field of chemical engineering with extensive experience in quality assurance and validation within the biopharmaceutical sector. Currently serving as QA Validation Manager and previously as Sr Validation Engineer at Sutro Biopharma, Inc. since April 2021, Zhimin has developed a strong foundation in validation processes. Prior experience includes roles as QA Validation Engineer II and Clinical Manufacturing Area Lead at BioMarin Pharmaceutical Inc. from August 2015 to April 2021, and a student intern position at California EPA. Additionally, Zhimin contributed as a student research assistant at UC Davis Department of Chemical Engineering and Materials Science from January 2012 to 2014. Educationally, Zhimin holds a Master of Science in Chemical Engineering from Stanford University (2019-2021) and a Bachelor's degree in Chemical Engineering and Biochemical Engineering from the University of California, Davis (2011-2015).
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Sutro Biopharma
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Sutro Biopharma is developing a new generation of multi-functional antibody drug conjugate therapeutics and bifunctional antibody-based therapeutics for targeted cancer therapies.