Ted Zhao Email & Phone Number | A methodical, practical and result-oriented pharmaceutical managing professional with all-around skills and track records in analytical sciences and pharmaceutical research & developments strives to make effective contributions and maximize team’s successes. • Over 20 years of experience in GMP/GLP environments and 10 years supervision experiences. • Managed analytical projects, internal and external labs, and supervised analytical professionals. • In-depth knowledge of 21CFR, FCC/FDA/DEA/ICH guidance and USP/EP/JP, OOS, Deviation and CAPA. • Proficient in authoring SOP, specifications, methods, validation/stability protocols/reports, and CMC documents. • Leading experience in analytical method development and validation, stability studies and release testing. • Experienced in U/HPLC, GC-HS, TLC, UV/Vis, FTIR, KF, TOC, Dissolution, LIMS, Trackwise, MS Office, etc. • Exceptional analytical and problem-solving skills, effective communication skills. Highly organized, result-oriented.

Ted Zhao

A methodical, practical and result-oriented pharmaceutical managing professional with all-around ski...
College Station, Texas, United States

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Ted Zhao’s Location College Station, Texas, United States

Ted Zhao’s Current Industry Fujifilm Diosynth Biotechnologies

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Quality Control Manager, Cell Biology

2022-06-01 00:00:00 - Present

Head Of Quality Control

2021-05-01 00:00:00 - 2022-04-01 00:00:00

Supervisor, Quality Control @ PharMEDium

2019-06-01 00:00:00 - 2020-04-01 00:00:00

Manager, Analytical Development & Quality Control

2017-11-01 00:00:00 - 2019-06-01 00:00:00

Manager, Quality Control

2011-02-01 00:00:00 - 2017-11-01 00:00:00

QC Scientist II

2009-05-01 00:00:00 - 2011-02-01 00:00:00

Sr. Scientist / Scientist I (Analytical Development and Quality Control)

2004-06-01 00:00:00 - 2009-03-01 00:00:00

Chemist

2003-10-01 00:00:00 - 2004-06-01 00:00:00

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Ted Zhao is a A methodical, practical and result-oriented pharmaceutical managing professional with all-around skills and track records in analytical sciences and pharmaceutical research & developments strives to make effective contributions and maximize team’s successes. • Over 20 years of experience in GMP/GLP environments and 10 years supervision experiences. • Managed analytical projects, internal and external labs, and supervised analytical professionals. • In-depth knowledge of 21CFR, FCC/FDA/DEA/ICH guidance and USP/EP/JP, OOS, Deviation and CAPA. • Proficient in authoring SOP, specifications, methods, validation/stability protocols/reports, and CMC documents. • Leading experience in analytical method development and validation, stability studies and release testing. • Experienced in U/HPLC, GC-HS, TLC, UV/Vis, FTIR, KF, TOC, Dissolution, LIMS, Trackwise, MS Office, etc. • Exceptional analytical and problem-solving skills, effective communication skills. Highly organized, result-oriented.

Ted Zhao has prior
experience in the following industries:
Molecular Templates | Amerisourcebergen | Fordoz Pharma | Aprecia Pharmaceuticals | Imclone Systems A Wholly Owned Subsidiary Of Eli Lilly | Nexmed | Ge Global Research

Ted Zhao has the following professional experience:
Fujifilm Diosynth Biotechnologies | Molecular Templates | Amerisourcebergen | Fordoz Pharma | Aprecia Pharmaceuticals | Imclone Systems A Wholly Owned Subsidiary Of Eli Lilly | Nexmed | Ge Global Research