This article was based on my session, Cleaning Validation Program Design: Risk-based Lifecycle Approach, delivered at the KENX’s Cleanroom Validation, Disinfection & Environmental Monitoring Conference April 27-29, 2022 Virtually and in person in Philadelphia, PA.
KENX’s hybrid conferences highlight those paving the way in best practices in cleanroom qualification, disinfection, contamination control, environmental monitoring and more.
Matthew Jackson
Validation Manager, Torbay Pharmaceuticals
Mr. Jackson is an experienced quality & validation manager with over ten years of experience in all areas of validation including; manufacturing and packing process/product validation, utility & facility validation, CSV, equipment qualification and cleaning validation. Recently appointed as Head of Quality, Matthew looks to promote the use of collaborative and strategic tools, to ensure a successful validation effort. In addition, Matthew has practical experience the use of quality tools for the management of complex validation & quality improvement projects within oral solid dose & sterile manufacturing facilities.
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