Trinh Trieu An is the Quality Assurrance & Regulatory Affair Manager at USM Healthcare Medical Devices Factory JSC. An received his Bachelor of Engineering in Mechatronic from the University of Technology, Ho Chi Minh and has been working with the team since 2014.
He began his career working as a Reseach & Develop Engineer. He has had experience in almost every aspect of project development including design & development, production, quality control, and quality assurance system. As a Quality Assurance & Regulatory Affair Manager, he is responsible for managing and directing the quality system at the plan level to comply with Competence Authorities requirements, all international standards such as ISO 9001, ISO 13485 and GMP-WHO and customer requirements as well. He maintains high standard of customer service to include investigation and resolution of quality complaints. He manages the regulatory affairs processes and final submission (Vietnamese Competence Authorities, CE applications product registrations, Asean countries applications product registrations,…) for medical devices approval and works to ensure compliance with application regulations and standards.
In his free time, An love to play football, go for hike and be outdoors. An enjoys expanding his skill sets, reading, traveling, and spending time with his friends and family.