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Responsibilities:
1. Carry out various quality management work under the leadership of QA Manager
2. Be responsible for the dynamic inspection of the production site to ensure that all key quality control points in the whole production process are under monitoring;
3. Be responsible for drafting and revising quality system documents related to the scope of supervision;
4. Assist in the investigation and handling of relevant deviations, complaints and other activities;
5. Participate in GMP self inspection activities, implement rectification measures and supervise the implementation;
6. Supervise and inspect whether the standard, reference, reagent and test solution are kept, used, stored and distributed according to the requirements, and assist and urge the workshop to solve the actual GMP problems
7. Irregular GMP inspection and annual self inspection of the Department
8. Make the work month analysis report as required, and report to the department head in time
9. Have high ideological quality and strong sense of responsibility, constantly learn business knowledge and improve working ability
10. Complete other tasks assigned by superiors

Qualifications:
1. College graduate or above in pharmacy, chemistry, biology, analysis and other related majors;
2. Solid pharmaceutical knowledge, familiar with basic GMP knowledge;
3. Work conscientiously and carefully, be proactive, and be steady and steady;
4. Familiar with GMP related regulations

Responsibilities:
1. Responsible for the analysis of the company's auxiliary materials, packaging materials, finished products and other instruments, physical and chemical, microbial index inspection
2. In the inspection work, strictly implement the inspection management procedures, product quality standards and inspection operation procedures, and carefully fill in the inspection records and auxiliary data
3. Participate in the preparation and revision of quality standards and inspection operation procedures
4. Responsible for cleaning and maintenance of inspection instruments

Qualifications:
1. Be familiar with various office software, word, Excel, PPT, etc., and be able to use Excel for data processing;
2. Have a certain foundation in English, CET4 or above, and be able to use English software proficiently;
3. Get the experimental method, be able to independently complete the experiment (sample pre-treatment, solution preparation, etc.) and report the results;
4. Proficient in liquid chromatography, gas chromatography and data analysis;
5. Basically able to independently complete the drafting of validation scheme of analytical methodology and the collation of validation report;
6. Positive working attitude, serious and good at thinking; The experimental idea is clear and clear;
7. Have a certain foundation of analytical chemistry experiments; In the instrument position, be able to operate liquid chromatograph independently, and work experience in gas chromatograph is preferred
Major: Pharmacy, chemistry, biology, pharmacy, analysis, pharmaceutical preparations

Responsibilities:
1. Carry out various R & D tests in strict accordance with relevant test subjects and test plans, and fill in test records and test reports in time.
2. Be responsible for various data issued by the test;
3. Take good care of the test instruments and equipment, maintain them regularly and keep them properly to ensure that the test instruments are in good condition and the measurement values are accurate;
4. After the test, clean the site, arrange and place the test instruments and test data, maintain a clean and civilized working environment, and ensure that it is clean, sanitary and reliable;
5. Assist in other matters authorized by the superior, and timely complete the temporary work tasks assigned by the leader.

Qualifications:
1. Bachelor degree or above in pharmacy, chemistry and biology;
2. Solid knowledge of organic chemistry;
3. Experience in organic synthesis experiments;
4. Work conscientiously and carefully, be proactive, and be steady and steady; Have good safety awareness and teamwork spirit.
5. Once employed, the treatment will be preferential

Responsibilities:
1. Carry out various production technical work under the leadership of the production department manager
2. Assist the manager of the production department to prepare documents such as product process procedures and post operation methods
3. Be responsible for spot checking the production progress of the workshop and various production records, and summarizing and reviewing the production batch records
4. Enter the production workshop and be familiar with the production process
5. Cooperate with R & D and production for technical handover
6. Complete other tasks assigned by superiors

Qualifications:
1. College graduates or above majoring in pharmacy, chemistry, biology, pharmacy, analysis, chemical machinery, mechanical equipment and other related majors;
2. Solid professional basic knowledge;
3. Work conscientiously and carefully, be proactive, and be steady and steady; Have good safety awareness and teamwork spirit.

Responsibilities:
1. Be fully responsible for the daily production of the preparation workshop, organize and implement the production according to the production instructions, and complete the production tasks with quality and quantity guaranteed;
2. According to the production order, before production, check the batch number and inventory of corresponding raw and auxiliary materials and packaging materials, and supervise the process of material procurement, inspection and release;
3. Be responsible for the whole process production and quality management of drugs, and assist the quality assurance department in the inspection of product quality;
4. Make correct judgments and properly handle the problems on the production site in time;
5. Be responsible for the process technology management of the workshop, and do a good job in the supervision of process control points and production deviations; Be responsible for organizing the continuous optimization of production process and process to ensure the continuous improvement of efficiency;
6. Organize workshop personnel to analyze various problems and deviations or assist the quality department to carry out deviation investigation and cause analysis, and develop effective corrective and preventive measures;
7. Organize workshop personnel to complete daily cleaning and maintenance of equipment in the production area and production area as required;
8. Strictly abide by the company's management system, obey the work assignment, and abide by labor discipline.
9. Be responsible for the necessary induction training and continuous training for the workshop production related personnel;
10. Be responsible for organizing the team building of the departments in charge, formulating staff training plans, and ensuring the continuous optimization of talent echelons; Organize the preparation of the annual training plan of the Department and regularly monitor the implementation progress of the training plan.
11. Complete the regular performance evaluation of department staff as required;
12. Participate in GMP self inspection and implement rectification, ensure the compliance of production organization with laws and regulations, continue to optimize and improve the construction of GMP, EHS and other systems, ensure safe production management, and ensure the smooth passing of various audit certifications; Participate in the formulation and implementation of validation scheme and revalidation scheme;
13. Cooperate with other departments to complete other tasks assigned by superior leaders.

Qualifications:
1. College degree or above, major in pharmacy, pharmaceutical engineering, chemistry and other related fields;
2. At least 5 years of experience in workshop management in pharmaceutical enterprises. Experience in oral solid preparation workshop and gel workshop management is preferred;
3. Have their own management concepts and practical experience in team management and talent echelon construction;
4. Work conscientiously and responsibly, have strong communication skills and cooperation awareness, and strong pressure resistance ability.
5. Once employed, the treatment will be preferential