Zuwei Jin, PhD

Lisure Science
Principal Consultant
Zuwei Jin, PhD, is a Principal Consultant at Lisure Science. Zuwei has more than 25 years of experience in the life sciences industry. He was an industry consultant for the life sciences industry in Cognizant Technology Solutions (formerly Zenith Technologies) specializing in manufacturing execution systems (MES) and process automation systems (PAS). Prior to that role, he was an industry consultant for the life sciences industry with Emerson Automation Solution for six years, specializing in MES, process analytics, and advanced process control (APC). He also has 16 years with GE Healthcare Life Sciences (Cytiva) in different roles, from operation to engineering to product marketing. He has been involved in many engineering projects in the global life sciences industry and is well versed with best practices in the industry. He has a PhD in chemical engineering from Ohio State University. Zuwei joined ISPE in 2013.

Related Articles

Continuous Buffer Management System: Large-Scale Buffer Preparation
Sponsored Content
Continuous Buffer Management System: Large-Scale Buffer Preparation

Content originally published in Pharmaceutical Engineering® May/June 2024, Volume 44, Number 3.

Although traditional tank farm systems have long been the cornerstone of buffer preparation, they face challenges that have grown with the expansion of processing scale in the industry.  This article explores the concept of the continuous buffer management system (CBMS) as an...

Continuous Buffer Management System: Large-Scale Buffer Preparation
Features
Continuous Buffer Management System: Large-Scale Buffer Preparation

Although traditional tank farm systems have long been the cornerstone of buffer preparation, they face challenges that have grown with the expansion of processing scale in the industry.1

  • 1National Institute for Innovation in Manufacturing Biopharmaceuticals-BioPhorum. “Buffer Stock Blending System: A More Advanced Concept for Buffer Manufacturing.” BioPhorum....
Figure 1: Batch simulation using MVDA
Technical
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,...

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