Mark is a product development consultant with over a decade of experience in the Medical Device and Pharmaceutical sectors. As the Director of Engineering at PSN Labs, Mark leads the engineering department, offering invaluable support to clients in new product development, test method development, functional prototyping, contract manufacturing, and on-market remediation. His team specializes in designing devices that incorporate various design principles, including manufacturing, assembly, sustainability, biocompatibility, reprocessing, and reliability.
 Mark’s background encompasses the development of innovative healthcare solutions in areas such as drug delivery, surgical robotics, pharmaceutical packaging, and catheters. His expertise ensures patient safety and regulatory compliance throughout the design process. Mark holds a Bachelor of Science in Mechanical Engineering from Purdue University and a Master of Science in Mechanical Engineering from the University of Cincinnati.
As medical devices transition from product development into manufacturing, early design decisions around design requirements and production strategy can significantly impact operational efficiency, cost, quality, and time to scale. This presentation describes an engineering driven approach to designing medical devices for process robustness and clinical success by aligning material selection, operational processes, and validation planning from the outset. Emphasis is placed on using design to improve operations through manufacturability, assembly, automation, and lights out readiness. This is articulated through a surgical device case study that includes reshoring considerations, reduced process variability, and improved manufacturing KPIs such as yield, cycle time, labor content, and scrap. Attendees will learn how early, intentional design choices enable faster operational response to material or process changes while minimizing risk during the transition to sustained manufacturing.