Zuwei Jin, PhD

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Zuwei Jin was a Senior Industry Consultant with Zenith Technologies. He specializes in manufacturing execution systems (MES), data analytics, and advanced process control (APC). He previously worked for Emerson Automation Solution for six years and GE Healthcare Life Sciences for 16 years. Zuwei’s technical experience includes biological production processes, cGMP hygienic equipment, process automation, data analytics, and operation management automation solutions. Zuwei has been involved in many engineering projects in the life sciences industry and is well versed with the best practices and various industry standards relevant to pharmaceuticals and automation. He has a PhD in chemical engineering from Ohio State University. Zuwei has been an ISPE member since 2013.

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Continued Process Verification in Stages 1–3

Continued process verification (CPV) as defined in the US FDA process validation guideline1 helps bring quality management and compliance in the pharmaceutical industry to the next level, but it has been challenging to...

  • 1US Food and Drug Administration. “Guidance for Industry. Process Validation: General Principles and Practices.” 2011. https://www.fda.gov/media/71021/download