Duong Dang is a seasoned QA/RA Specialist and R&D Engineer with approximately 13 years of experience in the medical devices sector, focusing on compliance, safety, and quality. From 2013 to 2021, Duong worked at Terumo Medical Corporation as a Design and Development Supervisor, where they led quality management systems and project management processes. Duong subsequently took on the role of Regulatory Affairs Lead at HCLTech from 2021 to 2024, preparing and reviewing regulatory documents for submissions to the FDA. Currently, Duong serves as a Senior Quality Assurance Specialist at Vantive, overseeing QA operations in Vietnam and Myanmar. Duong holds a Bachelor's degree in Advanced Chemistry from Vietnam National University and a Master's degree in Medicinal and Pharmaceutical Chemistry from Université de Rennes I.
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