YK

Yumi Kim

Manager, Regulatory Affairs - Product Development & Post Approval at Sagent Pharmaceuticals, Inc.

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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Timeline

  • Manager, Regulatory Affairs - Product Development & Post Approval

    March 1, 2022 - present

  • Manager, Product Development / Project Management

    January, 2019

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