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Paul Chow Location
Hong Kong
Paul Chow Work
Director of Manufacturing Operations and Authorized Person (GMP) @ (September 2024 - Present)
Authorized Person (GMP) and Leader in GMP Site Project Management @ (June 2020 - October 2024)
Deputy Authorized Person and Head of Regulatory Affairs @ Luxembourg Medicine Co., Ltd. (August 2018 - May 2020)
Authorized Person @ The United Laboratories Ltd. (May 2016 - August 2018)
QA Manager @ (September 2015 - May 2016)
Assistant General Manager - GMP (Authorized Person) @ (July 2012 - April 2015)
Authorized Person @ (February 2010 - June 2012)
Manager - Research and Regulatory Affairs Manager @ Jacobson Medical (HK) Ltd (January 2006 - January 2010)
QA Manager and Authorized Person @ Apotec Pharmaceutical Limited (formerly known as Merck Pharmaceutical Limited) (January 2003 - January 2006)
Paul Chow Education
The Chinese University of Hong Kong
Bachelor of Pharmacy (Pharmacy)
School Of Pharmacy , Cuhk
Paul Chow Skills
GMP
Regulatory Affairs
Pharmaceutical Industry
Quality Assurance
GLP
FDA
Biotechnology
Quality System
Life Sciences
CAPA
Pharmaceutics
SOP
Validation
Technology Transfer
Clinical Trials
Change Control
ISO 9001
Cold Chain Management
Paul Chow Summary
Paul Chow, based in Hong Kong, is currently a Director of Manufacturing Operations and Authorized Person (GMP) at Xellera Therapeutics. Paul Chow brings experience from previous roles at Xellera Therapeutics, Luxembourg Medicine Co., Ltd., The United Laboratories Ltd. and CSL Behring. Paul Chow holds a Bachelor of Pharmacy in Pharmacy @ The Chinese University of Hong Kong. With a robust skill set that includes GMP, Regulatory Affairs, Pharmaceutical Industry, Quality Assurance, GLP and more. Paul Chow has 2 emails and 1 mobile phone numbers on RocketReach.
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