Position Responsibilities: 

1. Assist the department manager to complete the certification of the quality system, with the external audit inspection, the organization of the company's relevant departments, the implementation of inspection implementation and coordination work;

2. Organize the company's internal product audit, accept the abnormality report form, cause investigation of the responsible department, issue abnormality processing report, put forward corresponding improvement opinions for non-conforming products;

3. Statistics on the completion status of quality targets in each department, analyze the reasons for not reaching the quality targets in conjunction with relevant departments, and track the implementation measures of the targets;

4. Responsible for on-site inspection and production process monitoring and abnormal occurrence of the implementation of follow-up corrective measures;

5. Supervise the production site, monitor the key steps and special processes, and keep records;

6. Complete other work assigned by the leadership. 

Position Requirements: 

1. Bachelor degree or above in biology, medicine, pharmacy or other related majors;

2. 1 year or above related work experience, with document QA management experience preferred;

3. Have quality system internal auditor and other related quality professional certificate is preferred;

4. Strong sense of responsibility, good communication skills, adaptability and ability to promote work.

Position Responsibilities: 

1. Responsible for the management, maintenance and periodic calibration of monitoring and measuring devices; responsible for the management of measuring instruments, preparation of measuring instrument calibration plans,

timely delivery of measuring instruments to the higher metrology department for inspection and maintenance of original records of calibration;

2. Familiar with inspection procedures, conformity inspection and testing of purchased products, intermediate products, final products and the environment, forming records and issuing inspection reports; exercising authority independently and making conclusions, and being responsible for the accuracy of the conclusions;

3. To manage product retention samples and carry out testing in accordance with the prescribed cycle;

4. Responsible for establishing, recording and keeping inspection records; and organizing and filing regularly;

5. Responsible for the acceptance of medical device related instruments; collection and collation of inspection reports; moving instruments;

6. Other work assigned by the leadership. 

Position Requirements: 

1. Bachelor's degree or above in medicine, laboratory science, biology, immunology or pharmacology and other majors

related to the products produced;

2. Having at least 1 year of quality inspection work experience or excellent fresh graduates;

3. Strong practical skills, critical working, high quality consciousness and work responsibility.

Position Responsibilities: 

1. Completing experiments, writing process records and analyzing experimental results according to experimental protocols;

2. Assist in completing the output of technical documents; be able to complete reagent preparation, experimental operations and experimental reports independently;

3. Submitting experimental results and reporting experimental progress in a timely manner;

4. Responsible for data recording, result analysis and report writing of experiments;

5. Assist in completing other work. 

Position Requirements: 

1. College degree or above in biology, medicine, pharmacy, medical testing related majors, excellent fresh graduates are also eligible;

2. Patient, practical and willing to learn, proactive, strong sense of responsibility and team spirit.

Position Responsibilities: 

1. Strictly implement production in accordance with production plans and production process protocols to ensure that the production process meets regulatory and technical requirements;

2. Follow up the whole process of verification of key equipment, responsible for the development and implementation of process protocols;

3. Responsible for the production process abnormal situation and investigation for analysis, and propose feasible solutions;

4. Responsible for the revision of the operating procedures of products related to the conversion process and the improvement of existing operating procedures;

5. Responsible for the production of various processes data summary and statistical analysis. 

Position Requirements: 

1. College degree or above in medicine, biology, medical devices and other related majors;

2. More than 1 year working experience in biopharmaceutical production;

3. Priority consideration for those with relevant industry work experience.