Jo Tse is an experienced professional in pharmaceutical operations, specializing in program and risk management, quality assurance, and supply chain optimization. They served in various capacities at GSK from 2016 to 2017, including Serialisation & Artwork Director and Site Validation Manager, where they led critical projects ensuring regulatory compliance and quality management. Currently, Jo is a Pharmaceutical Consultant at JTiPS, providing transformative strategies within the pharmaceutical landscape, and serves as the Regional Lead for the Product Transformation Office at Vantive, overseeing significant drug and device management across the APAC region. Jo holds an MSc from the University of Leicester and a BSc (Hons) from Nottingham Trent University, with further education from Stanford University's Graduate School of Business.
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