Andy Moyes is a Certified Industrial Sterilization Specialist (CISS-CORE) with more than 10 years of experience spanning medical device manufacturing, quality operations, and sterilization validation. He possesses extensive expertise in ethylene oxide (EO) sterilization, validation strategy, regulatory compliance, and continuous process improvement within highly regulated healthcare and life sciences environments.
In his previous role as a Validation Engineer, Andy led EO sterilization equipment and process validation projects, overseeing the development and execution of IQ, OQ, and PQ protocols while providing technical guidance and mentorship to validation engineering teams. His experience includes ensuring compliance with ISO 11135, FDA, and GMP requirements, delivering robust validation solutions that support regulatory excellence and customer success.
Throughout his career, Andy has demonstrated a strong commitment to operational excellence and process optimization, leveraging Lean Six Sigma and 6S methodologies to improve efficiency and reduce lead times. His industry experience has strengthened his ability to drive quality-focused outcomes in complex manufacturing and sterilization environments.
Andy holds a Bachelor of Science degree in Exercise & Sport Science with an emphasis in Physiology and Chemistry from the University of Utah College of Health. He is currently pursuing his CISS-EO certification and remains dedicated to advancing sterilization science, validation best practices, and quality assurance across the medical device industry.
