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Brian Benson is an experienced professional in validation and quality assurance, currently serving as Validation Project Lead at Grand River Aseptic Manufacturing since March 2018. With a career spanning several companies, including Cayman Chemical as a QA & Validation Engineer, Brian has expertise in calibration, qualification of GMP equipment, process validation, and enhancement of quality systems. Prior roles include Senior Validation Consultant at LexaMed, Validation Manager at CH2M HILL and SSOE, Inc., and Regional Validation Manager at Washington Group International, demonstrating a strong background in managing validation teams and projects. Brian holds an AAS in Electromechanical Engineering Technology from Michigan Technological University.