Regulatory and Quality
Todd Evans, Senior Director Quality and Regulatory Affairs
Todd is responsible for Quality and Regulatory Affairs for OsteoCentric Technologies. Todd brings over 24 years of experience in the medical device industry. Before joining OsteoCentric Todd was the Director of Quality and Regulatory Affairs at Thermo Fisher Scientific, where he was responsible for over 110 quality professionals across 5 global manufacturing sites. Todd started his career in validation and quality engineering where he was directly involved in product development, supplier quality, complaint investigations, managing corrective and preventative actions, and sterilization processes. During his leadership tenure he was also involved in lean manufacturing, quality metric development, global harmonization, regulatory, and customer relations. Todd has a strong background in ISO13485, 21CFR 820, 21CFR 210, and 211 and holds a Bachelor’s degree in Biology from Utah State University.
Ismael Sagredo, Quality Engineer
As a Quality Engineer, Ismael works to maintain the highest standard of product for our patients and users. Ismael had spent 2 years in Orthopedics and holds a Master’s in Biomedical Engineering from the University of Texas at San Antonio. Prior to OsteoCentric, Ismael held an intern position in the R&D department of Biomedical Enterprises – Depuy Synthes.