Gary Avedovech

Gary Avedovech has extensive work experience in the field of regulatory compliance and quality assurance in the medical device industry. Gary'smost recent role was as the Regulatory and Quality Assurance Director at Tribeca Companies, where they started in November 2022. Prior to that, they worked as the Senior Director of Quality and Compliance at Spartan Micro from September 2020 to November 2022. From 2017 to 2020, they served as the Manager of Quality and Compliance at Medrio.

Before joining Medrio, Gary Avedovech had a managerial role at Medical Device Engineers & Consultants Group, where they initiated the Medical Device focus group on LinkedIn in 2008. Additionally, they worked at Electroblate as a Quality Engineer and Quality Manager, where they were responsible for establishing and improving the quality system while developing new medical technology.

Gary also gained valuable experience in process validation and quality assurance through their roles as a Consultant Engineer at Genentech, a Quality Engineering position at a startup in San Francisco, and a Process Validation Consultant at a medical device company through Globiox. Gary has demonstrated expertise in compliance, risk assessment, and validation protocols.

Earlier in their career, Gary Avedovech served as the Senior Manager of Quality Assurance at Pulsar Vascular, where they led efforts to achieve ISO 13485 and MDD Annex II part 3 certifications. Gary also worked as a Process Validation Consultant at Celera Corporation, where they assessed validation protocols and recommended improvements.

Gary Avedovech has a Bachelor of Science in Mechanical Engineering from Arizona State University, which they obtained in 1996. Gary also attended Green Mountain High School from 1985 to 1989. In terms of certifications, they obtained the Certified Quality Auditor (CQA) certification from the American Society for Quality in December 2023 and the Certified Quality Engineer (CQE) certification in July 2014.