Job description:

1. Familiar with the quality management process of three kinds of medical devices;

2. Familiar with the internal production and operation process of production-oriented enterprises, and skillfully use various quality improvement tools and technologies for quality analysis;

3. Have a deep understanding of ISO13485 quality system certification of medical product quality management system, and have ISO13485 internal auditor certificate;

4. Maintain quality system;

5. Coordinate all departments to carry out continuous quality improvement activities;

6. Participate in risk management activities;

7. Responsible for the internal and external quality audit, preside over the annual internal audit and management review, and track the corrective and preventive measures for non conformance items

。 Responsible for checking and evaluating the operation of quality system to ensure continuous improvement of management and effective operation of quality system;

8. Organize GMP knowledge training and SOP training for employees;