Adept in medical device productregistration and leading quality management initiatives,

Responsible for planning, organizing, and implementing the domestic registration of company products, developing product registration strategies, collaborating on research and development to prepare product technical requirements and other related testing/registration technical documents; Coordinate registration project resources and effectively promote the development of registration work;

2. Assist superiors in organizing internal registration management within the company, assist in establishing the necessary management system for registration, and establish and maintain a database of relevant product registration documents;

3. Timely understanding of changes in medical device regulations, real-time access to newly released and revised laws and regulations, and grasp the policy orientation and approval principles of product registration and application;

4. Collect, organize, and update the laws, regulations, and product standards related to the company, provide consulting advice for new product registration or certification strategies, and ensure product regulatory compliance after listing;