Job Responsibilities:

　　1. Responsible for the strategic design and implementation plan drafting of the registration project of imported pharmaceuticals and medical device products;

　　2. Participate in external project negotiations, provide professional opinions and suggestions from the perspective of product registration compliance and feasibility, and participate in negotiations with foreign parties, and receive and confirm registration materials;

　　3. Complete the registration and application of imported products, including document writing, document submission, post-acceptance tracking and communication, sample registration inspection, research and development site inspection, etc.;

　　4. Follow up, collect and sort out product registration regulations, analyze their possible impact on the project or enterprise, and adjust the registration plan accordingly or propose a solution;

　　5. Responsible for the coordination and management of external entrusted registration projects;

　　6. Complete other related tasks arranged by the leader.

　　Qualifications:

　　1. Major in medicine or pharmacy, master's degree or above; graduation from the Japanese Pharmacy Class of Pharmaceutical University is preferred;

　　2. More than 5 years of pharmaceutical registration and application experience, working experience in a foreign-funded pharmaceutical company or experience in leading a registration team is preferred. Experience in developing and registering imported drugs in China and obtaining import registration certificates;

　　3. Good foreign language skills (CET-6).