1. Plan, implement and coordinate activities related to quality system, quality assurance, quality verification, customer problem handling and daily management of the department. 2. Collection and update of domestic/foreign medical device regulatory certifications and related regulations and standards. 3. ISO13485 and GMP quality system audit related matters. 4. Matters related to domestic/foreign medical device clinical trials.
Responsible for the management of the diffusion engineering department's goals: 1. Plan, introduce and accept new process technologies, equipment or materials. 2. Plan and evaluate the optimal production mode configuration of various types of machines in the department. 3. Plan and evaluate process stability and machine uptime improvement plans. 4. Planning and introduction of department automation system 5. Human resource management and development of the units under its jurisdiction 6. Tasks assigned by superior supervisors