Russell J. Morrison, MBA, CPIP

Rusty Morrison is an experienced pharmaceutical professional with over 30 consecutive years of experience at all levels in technology transfer, CMC project management, process validation, commissioning, qualification, validation, engineering, and manufacturing. Significant biopharmaceutical experience includes managing a bulk drug substance site-to-site tech transfer; managing early-stage RNA interference CMC activities for multiple products in the development pipeline; multiple assignments managing teams providing risk-based validation, commissioning, and engineering services for mammalian cell culture facilities; and serving as Director of Facilities & Engineering for a startup vaccine manufacturer. Other relevant experience includes leadership of a team responsible for all process validation protocols for the start of commercial operations at one of the largest mammalian cell culture facilities in the U.S.; including protocol generation, execution, deviation resolution, and report preparation.