Job Responsibilities:

1. Responsible for writing and reviewing registration materials, submitting registrations, and following up on registration progress;

2. Coordinate with overseas agents and regulatory authorities, and respond promptly to requests for correction and correction;

3. Collect and interpret overseas registration regulations, and pay attention to regulatory trends;

4. Establish and maintain international registration project archives, and maintain the validity of certificates;

5. Handling emergencies and other tasks assigned by superiors.

Job Requirements:

1. Bachelor's degree or above, with a preference for majors in biomedicine, chemical materials, foreign languages, or related fields;

2. More than 1 year of work experience in international registration of medical devices, with priority given to those with independent overseas medical device registration and application experience;

3. Have a certain ability to organize and write information, ensuring the accuracy and completeness of registration materials;

4. Possess good communication, learning, and stress resistance abilities, as well as teamwork spirit.