Quality Engineer

1.Taking in charge of quality assurance of raw materials, process products, and final products, reviewing batch records. 2.On-site monitoring for all production related process, finding out and implementing CAPA, resolving on-site issues. 3.Following up non-qualified products under production process, and verifying the effectiveness of corrective actions. 4.Regularly conducting quality analysis of product and production process. 5.Handling customer complaints, timely conducting corrective and preventive measures, tracking and verifying results. 6.Following up the implementing status of annual production plan. 7.Implementing the ad-hoc assigned work.

1.Bachelor degree or above, major in medical device, materials science, pharmacology, medicine, chemical engineering, mechanical engineering, and automation is preferred. 2.3+ years quality engineer working experience on medical devices (Class II and/or III sterile medical device). 3.Fluent in English (written and oral).