The recruitment of Jiete Biological Testing Center, a listed company, is currently underway!

1. Responsible for the daily management of the microbiology laboratory, establishing, maintaining, and improving relevant management systems to comply with CMA, CNAS, and other management system requirements;

2. Lead microbiological testing technology work, including daily testing, testing method development, method validation, standard updates, etc., to comply with relevant laws and regulations such as the Chinese Pharmacopoeia and ISO standards, and complete CMA and CNAS qualification expansion verification tasks, providing customer technical services;

3. Analyze and investigate the causes of microbial contamination in leading products;

4. Responsible for the training, supervision, assessment, work arrangement, and daily management of personnel related to microbiology;

5. Responsible for reviewing records related to microbiological testing;

6. Responsible for environmental management of microbial areas;

7. Lead the maintenance and upkeep of equipment related to microbial areas;

8. Other tasks arranged by the leader.

1. Have 5 years of relevant work experience in microbiology laboratories of third-party drug inspection and testing institutions, and have more than 3 years of team management experience;

2. Bachelor's degree or above, majoring in microbiology, medicine, biopharmaceuticals, food science, bioscience, or related fields;

3. Proficient in the relevant testing methods and requirements of the Chinese Pharmacopoeia, including but not limited to sterility, bacterial endotoxins, microbial limits, etc., and have experience in developing and verifying methods for no less than 5 microbial testing items;

4. Good organizational and coordination skills, as well as teamwork spirit;

5. Familiar with CMA, CNAS and other management systems, and have relevant testing and expansion experience.

1. Responsible for the company's quality management work, ensuring the implementation of quality policies and objectives;

2. Responsible for establishing, maintaining, operating, and improving the quality management system, as well as effectively carrying out quality management work;

3. Lead the application for CMA, CNAS qualifications and other qualifications;

4. Organize the preparation, revision, and promotion of quality system documents;

5. Responsible for developing and implementing internal management system management reviews and management review plans;

6. Lead the preparation of relevant work for external quality inspection and flight inspection, and track the corrective measures for non conformities;

7. Supervise the implementation of the annual plans of each department of the company and collect relevant records;

8. Promote the company's 5S management;

9. Complete other work tasks assigned by superiors.

1. Bachelor's degree in Chemistry, Biology, Pharmacy or related majors;

2. Work in the third-party inspection and testing industry for more than 5 years, and have more than 3 years of team management experience;

3. Understand the professional knowledge within the scope of the testing work carried out by the institution;

4. Familiar with CMA, CNAS and other management systems, and have experience in organizing inspection and testing project expansion;

5. Possess CMA, CNAS related training certificates or other supporting materials;

6. Able to withstand certain work pressure and possess good teamwork spirit.

7. Experience in leading CNAS expansion projects in the pharmaceutical field is preferred.

1. Carry out testing of samples of packaging materials such as drugs and food;

2. Carry out verification of testing methods and research on packaging material compatibility;

3. Complete the CMA and CNAS qualification expansion verification tasks;

4. Maintain and manage testing equipment and laboratory environmental facilities;

5. Teach newcomers;

6. Complete other work tasks assigned by superiors.

1. Bachelor's degree or above in chemistry, biology, pharmacy or related majors, with more than 5 years of experience in packaging material physical and chemical testing and at least 3 experiences in packaging material compatibility research;

2. Proficient in operating instruments and equipment for drug packaging material testing, familiar with relevant standards for drug packaging materials;

3. Have experience in third-party testing institutions for pharmaceutical packaging materials, familiar with management systems such as CMA and CNAS, and have relevant testing expansion experience.