Steve Kilburn

Steve Kilburn has over 23 years of experience in the medical device and healthcare industries. Steve began their career in 1995 as a Supplier Quality Engineer at Bausch + Lomb. From 1998 to 2011, they worked at Meridian Medical Technologies, where they held the roles of Director - Product Technology / Supplier Quality and Sr. Manager QA/QC. During this period, they were responsible for overseeing staff of 7 engineers/project managers for cGMP compliance, leading global cross functional teams during “for cause” audits at supplier manufacturing locations, and managing the Supplier Quality program. In 2011, they started a home improvement business and also held the role of Sr. Manager QA/QC at bioMérieux. From 2017 to 2019, they were a FDA Compliance Consultant - Medical Device/Combination Products at Phillips Health Care Products and V.P. Quality & Regulatory Affairs at inx Medical. Since 2018, they have been a Senior Quality & Regulatory Consultant at NeoGenomics Laboratories and, more recently, Vice President of Quality at TriSalus Life Sciences.

Steve Kilburn received a Master of Business Administration (M.B.A.) from Washington University in St. Louis in 2000, and a Bachelor's Degree in Manufacturing Engineering from Southeast Missouri State University in 1991.