Christopher Cruz

Christopher Cruz has over 17 years of experience in quality assurance and document control within the medical device industry. At IRRAS USA Inc., Christopher started as a Document Control Specialist in July 2022 and transitioned to a Quality Assurance Specialist after one year. Prior to this role, Christopher worked at Organogenesis Inc. from April 2007 to December 2021, serving as a Quality Control Analyst responsible for cGMP incoming inspections and raw material disposition for Class II medical devices compliant with FDA, ISO, and AATB regulations. Christopher attended UC Irvine from 2001 to 2003.