Matthew K.

Matthew K. is an experienced professional in the field of quality management and process validation, currently serving as the Associate Director of Third Party Quality Management Drug Product at Merck since 2025. Previously, they held various roles at Bristol Myers Squibb, including Manager and Senior Validation Engineer I within the CAR T department, where they managed validation strategies and coordinated process improvement projects. Matthew's earlier experience includes positions at Celgene and Pepperidge Farm, where they contributed to quality control and research development. They have a strong background in regulatory compliance and team leadership, having trained numerous associates and streamlined operational processes in the field of cell therapy.