Jason has over 20 years of experience working in research and development, validation, and routine control of various sterilization processing modalities, including, but not limited to, steam, ethylene oxide (EtO/EO), dry heat, and H2O2 gas plasma sterilization. His experience includes the commissioning of sterilization vessels for clients, including IQ, OQ, and PQ performance.
He is a certified quality auditor and specializes in providing consultations for clients about the sterilization of reusable medical devices, endoscopes, and pharmaceutical products. He also consults on general sterilization validation process development. As a member of the American Association of Medical Instrumentation (AAMI), Jason plays an active role, in collaboration with the FDA and regulatory committees, in developing standards and voting on changes to those standards.
