Yumi Kim has extensive work experience in the pharmaceutical industry. Yumi started their career as an Intern at Argonne National Laboratory in 2000. Yumi then worked at Abbott as a QA Sr. Laboratory Analyst from 2001 to 2003. Yumi joined Hospira in 2003 as an Associate Scientist. After that, they worked at NantPharma Inc. in various roles, starting as a Scientist in 2006 and progressing to Senior Scientist and Principal Scientist in Biomolecular R&D until 2016. Yumi then joined NantKwest as a QA Manager for Global Cell Therapy Manufacturing from 2016 to 2018. Prior to their current role, Yumi worked at Sagent Pharmaceuticals as a Manager for Product Development / Project Management from 2019 to 2022, and is currently employed as a Manager for Regulatory Affairs - Product Development & Post Approval.
Yumi Kim has a Master's Degree in Biotechnology and Chemical Sciences from Roosevelt University. Yumi also holds a Bachelor's Degree in Chemistry from the University of Illinois Urbana-Champaign.
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