Paul Chow

Authorized Person (GMP) / Head of QA / Leader in GMP Site Project Management at Xellera Therapeutics

Paul Chow has over 17 years of work experience in the pharmaceutical industry. Paul most recently worked at Xellera Therapeutics as an Authorized Person (GMP), Head of QA, and Leader in GMP Site Project Management. Prior to that, they served as the Deputy Authorized Person and Head of Regulatory Affairs at Luxembourg Medicine Co., Ltd. Paul also held the position of Authorized Person at The United Laboratories Ltd. and QA Manager at CSL Behring. Paul has extensive experience at New B Innovation Ltd, where they worked as Assistant General Manager-GMP (Authorized Person) and later as an Authorized Person. Paul began their career at Jacobson Medical (HK) Ltd as a Manager in Research and Regulatory Affairs and also served as QA Manager and Authorized Person at Apotec Pharmaceutical Limited (formerly known as Merck Pharmaceutical Limited).

Paul Chow's education history includes a Bachelor of Pharmacy degree from The Chinese University of Hong Kong. Paul also attended the School of Pharmacy at CUHK, although specific dates and degree information for this period are not provided. In addition to their educational background, Paul has obtained additional certifications, including a Six Sigma Green Belt from SGS in March 2020 and an Authorized Person certification from the Pharmacy and Poisons Board of Hong Kong in September 2015.

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  • Authorized Person (GMP) / Head of QA / Leader in GMP Site Project Management

    June, 2020 - present