Job description: 1. Responsible for arranging the product registration plan, tracking the registration process, including the collection, sorting, writing, application and progress tracking of registration data, and solving problems encountered in the research and application process. 2. Be responsible for formulating product clinical trials and analyzing clinical data. 3. Be responsible for communicating with relevant government functional departments, including product testing departments, to ensure smooth application. 4. Assist in establishing the quality management system of medical device manufacturers and assist them to pass the quality management system verification of relevant regulatory authorities. Job requirements: 1. Bachelor degree or above in biomedicine, bioengineering, agronomy, veterinary medicine and other related majors. 2. In vitro diagnostic reagent registration, Class II registration and Class III registration. 3. More than 1 year of experience in quality system management or product registration related positions in IVD reagent companies (including but not limited to chemiluminescence, POCT, biochemistry, ELISA, etc.), and experience in product registration of the whole line is preferred. 4. Be familiar with the registration process and regulations of IVD medical devices, and have certain English reading and writing skills. 5. Strong initiative, careful and meticulous, good team spirit and communication ability. 6. Strong ability to compile registration documents and relevant materials. 7. In vitro diagnostic instrument product registration or ISO13485 quality management system experience is preferred.