Paige Kane, PhD, CPIP, is a Director in the Merck Manufacturing Division, and a member of the MMD Knowledge Management (KM) Center of Excellence. She is an industry leader with over 30 years of experience, including with six pharmaceutical companies and the US government, spending the past 13 years designing and leading KM programs and approaches for the Pharmaceutical Industry. Prior to her work in KM, Paige led multiple quality systems groups focusing on automation compliance strategies, change control, document management, computer/equipment validation and data integrity for new biotechnology facility start-ups and operations in the US and Ireland. She has experience working across the pharmaceutical product lifecycle in GLP, GCP (clinical trial oversight and supplies), and GMP in human and animal health.
Paige has led several industry strategic teams including ISPE CoPs, and currently leads the ISPE KM Good Practice Guide authoring team. Paige has participated in authoring several industry guidance documents and contributed to many conference sessions and industry papers. She is a co-editor of, and multi-chapter contributor to, ‘A Lifecycle Approach to Knowledge Excellence in the Biopharmaceutical Industry’ (2018).