Job Responsibilities:

1. System document management: document formulation, issuance, cancellation and preservation;

2. Supervise relevant departments and personnel to implement regulations, rules and norms of medical devices to ensure quality

3. Assisted the quality manager to carry out quality management training;

4. Completed product acceptance and process inspection;

5. Participate in the implementation of verification and validation;

6. Other quality-related matters.

Job Requirements:

1. Bachelor degree or above in life science;

More than 1 year quality work experience;

3. Familiar with the production and sales process of medical devices and relevant rules of ISO13485;

4. Good team spirit and rigorous working attitude, able to work under pressure.