Yi Feng

Yi Feng has extensive experience in quality assurance and regulatory compliance within the medical device industry, currently serving as the Post Market Quality Team Lead at Cochlear since January 2003. Responsibilities include ensuring adherence to regulatory reporting requirements for post market surveillance, managing the completion of PMS plans and reports, and collaborating with cross-functional teams to analyze product data. Previous roles at Cochlear include Senior Post Market Quality Specialist, Complaint Specialist, and Senior Reliability Analysis Technician, contributing to product quality monitoring and reliability characterization. Prior experience includes leadership roles at BP and Tanabe Seiyaku Pharmaceutical, with a foundational education in Engineering/Industrial Management from China Pharmaceutical University and further studies at TAFE NSW.