Steven D Kehoe takes a meticulous and technically-driven approach, focusing on the compliance and quality aspects of pharmaceutical manufacturing. He looks for a solid foundation in documentation, process validation, and equipment qualification, and expects a robust oversight in training and qualification of personnel across various technical processes.

Steven D Kehoe focuses heavily on the technical aspects of pharmaceutical manufacturing and quality control, particularly in areas such as document management, sample testing, process validation, equipment qualification, and batch manufacturing. He expects thorough adherence to established procedures, rigorous training and qualification processes for laboratory analysts, and robust oversight in corrective and preventive actions (CAPA).