Job Responsibilities:

1. Responsible for collecting on-site quality data, analyzing it, proposing improvement measures, and following up;

2. Follow up on the trial production of new materials and molds in the workshop, provide guidance and supervision on trial mold samples and engineering changes on site;

3. Provide professional knowledge training on relevant positions for workshop IPQC:

4. Responsible for 6S management related affairs, organizing, coordinating, promoting, compiling, training and other related work;

5. Complete other tasks assigned by superiors.

Job Requirements:

1. Bachelor's degree or above;

2. More than 2 years of relevant work experience, familiar with ISO13485 medical device quality management system;

3. Strong judgment, decision-making, adaptability, and organizational coordination skills, as well as strong communication and coordination abilities;

4. Has a certain ability to organize text.