Post qualification:

1. Participate in the maintenance and continuous improvement of ISO 13485, GMP and other quality management systems;

2. Participate in the planning, preparation and implementation of internal and external audits of the company, and participate in the planning of various quality management activities;

3. Other relevant work arranged by the leader.

Qualifications:

1. College degree or above, major in medical engineering or other related fields;

2. At least 1 year of working experience in medical device quality management system;

3. Familiar with ISO 13485 and GMP quality management system requirements;

4. Good communication and writing skills; Strong sense of responsibility, meticulous and responsible work, and team spirit;

5. Internal auditor certificate is preferred.