Job Responsibilities:

1. Strictly implement product-related inspection procedures and operating procedures, complete inspection tasks, record and save experimental data in time, and judge and feedback inspection results;

2. Do a good job of mutual verification of the test results and test reports of the same class personnel in a timely manner.

3. Responsible for marking the unqualified products detected and reporting to the person in charge of quality in a timely manner, participating in the review of unqualified products, and issuing treatment opinions;

4. Responsible for the daily maintenance and calibration of the testing equipment of the department;

5. Responsible for maintaining the cleanliness of the laboratory environment and using consumables appropriately;

6. Assist in the establishment, revision and verification of testing methods for testing products.

Qualifications:

1. College degree or above, major in pharmaceutical preparations, biotechnology, pharmacy, pharmaceutical engineering and chemistry;

2. More than one year of preparation inspection work experience is preferred, and excellent fresh graduates in related majors are also available;

3. Familiar with the use, calibration and maintenance of conventional instruments, such as: HPLC, GC, UV, IR and dissolution, etc.;

4. Those who understand the pharmacopoeia, GMP and drug production management regulations are preferred;

5. Have a high sense of responsibility and initiative, and be able to make more accurate judgments and handling of quality problems;

Job Responsibilities:

1. Strictly implement product-related inspection procedures and operating procedures, complete inspection tasks, record and save experimental data in time, and judge and feedback inspection results;

2. Do a good job of mutual verification of the test results and test reports of the same class personnel in a timely manner.

3. Responsible for marking the unqualified products detected and reporting to the person in charge of quality in a timely manner, participating in the review of unqualified products, and issuing treatment opinions;

4. Responsible for the daily maintenance and calibration of the testing equipment of the department;

5. Responsible for maintaining the cleanliness of the laboratory environment and using consumables appropriately;

6. Assist in the establishment, revision and verification of testing methods for testing products.

Qualifications:

1. College degree or above, major in pharmaceutical preparations, biotechnology, pharmacy, pharmaceutical engineering and chemistry;

2. More than one year of preparation inspection work experience is preferred, and excellent fresh graduates in related majors are also available;

3. Familiar with the use, calibration and maintenance of conventional instruments, such as: HPLC, GC, UV, IR and dissolution, etc.;

4. Those who understand the pharmacopoeia, GMP and drug production management regulations are preferred;

5. Have a high sense of responsibility and initiative, and be able to make more accurate judgments and handling of quality problems;

Job Responsibilities:

1. According to the company's development goals, formulate production system work goals and production plans, and effectively adjust production indicators according to the production plan and the safety stock of finished products;

2. Supervise the workshop production in accordance with the production plan, review batch production instructions and batch production records;

3. Coordinate various work in the production process, properly handle various emergencies in time, and ensure the smooth progress of production work;

4. Organize the workshop to conduct a comprehensive statistical cost accounting for various production data, and summarize the audit reports;

5. Manage production equipment, allocate and allocate reasonably, and assist relevant departments in handling the depreciation, damage, and scrap of production equipment;

6. Carry out the national pharmaceutical regulations and relevant technical regulations of superiors, review the process regulations and related documents, manage and guide the production technology and process, and properly handle and solve the technical problems in production in a timely manner;

7. Guide the construction of the production system GMP management system for self-inspection and maintenance; strictly implement GMP documents to ensure that the work is traceable;

8. Strictly implement the production safety management system to ensure the safe operation of various equipment;

9. Responsible for the allocation and selection of production staff, organize skill training for production departments, grasp the ideological trends of employees, guide subordinates to efficiently implement target requirements and work tasks, and conduct performance assessments in a timely and fair manner.

10. Responsible for organizing the evaluation, design, debugging, and use of new production lines and new equipment, and effectively organize the production transfer of new products;

Qualifications:

1. Bachelor degree or above, major in pharmaceutical engineering, pharmacy, chemistry, biological preparations, etc.;

2. More than 10 years of experience in preparation production management, more than 3 years of work experience in the same position, working experience in a large pharmaceutical company is preferred;

3. Familiar with the production and manufacturing operations and processes of pharmaceutical preparations, good at production control and on-site management, production operations and management, and have strong planning execution, communication, analysis and judgment and resolution capabilities;

4. Have good professionalism and professional ethics, good appeal and cohesion.

5. Familiar with the laws and knowledge related to drug production, quality management, occupational safety, health, and environmental management systems;

6. Have a strategic vision, have a good sense of teamwork, good organizational management and coordination capabilities, and be good at handling relevant public relations;

7. Have a high sense of responsibility, excellent leadership, and be able to organize and manage the team efficiently.

Job Responsibilities:

1. According to the company's development goals, formulate production system work goals and production plans, and effectively adjust production indicators according to the production plan and the safety stock of finished products;

2. Supervise the workshop production in accordance with the production plan, review batch production instructions and batch production records;

3. Coordinate various work in the production process, properly handle various emergencies in time, and ensure the smooth progress of production work;

4. Organize the workshop to conduct a comprehensive statistical cost accounting for various production data, and summarize the audit reports;

5. Manage production equipment, allocate and allocate reasonably, and assist relevant departments in handling the depreciation, damage, and scrap of production equipment;

6. Carry out the national pharmaceutical regulations and relevant technical regulations of superiors, review the process regulations and related documents, manage and guide the production technology and process, and properly handle and solve the technical problems in production in a timely manner;

7. Guide the construction of the production system GMP management system for self-inspection and maintenance; strictly implement GMP documents to ensure that the work is traceable;

8. Strictly implement the production safety management system to ensure the safe operation of various equipment;

9. Responsible for the allocation and selection of production staff, organize skill training for production departments, grasp the ideological trends of employees, guide subordinates to efficiently implement target requirements and work tasks, and conduct performance assessments in a timely and fair manner.

10. Responsible for organizing the evaluation, design, debugging, and use of new production lines and new equipment, and effectively organize the production transfer of new products;

Qualifications:

1. Bachelor degree or above, major in pharmaceutical engineering, pharmacy, chemistry, biological preparations, etc.;

2. More than 10 years of experience in preparation production management, more than 3 years of work experience in the same position, working experience in a large pharmaceutical company is preferred;

3. Familiar with the production and manufacturing operations and processes of pharmaceutical preparations, good at production control and on-site management, production operations and management, and have strong planning execution, communication, analysis and judgment and resolution capabilities;

4. Have good professionalism and professional ethics, good appeal and cohesion.

5. Familiar with the laws and knowledge related to drug production, quality management, occupational safety, health, and environmental management systems;

6. Have a strategic vision, have a good sense of teamwork, good organizational management and coordination capabilities, and be good at handling relevant public relations;

7. Have a high sense of responsibility, excellent leadership, and be able to organize and manage the team efficiently.

Job Responsibilities

1. According to the production requirements, formulate a monthly production plan, and in accordance with GMP requirements, rationally schedule production and schedules, coordinate various production resources, and complete production tasks in a timely and safe manner with quality and quantity;

2. Check the implementation of product process regulations and operating regulations, deal with quality problems in the production process in time, organize quality analysis meetings and production coordination meetings to ensure product quality, complete product quality review, continuous process confirmation and other related work;

3. Develop effective workshop management methods, continuously improve GMP awareness, standardize production on site, and ensure that management is in place;

4. Strengthen the management of various materials in the production process, reduce material consumption and energy consumption, and reduce production costs while ensuring quality;

5. Responsible for the maintenance and maintenance of production equipment and facilities, so that the production equipment and facilities are in a good and operational state;

6. Responsible for the safe production of the workshop, eliminate hidden dangers of accidents such as personnel and equipment, and ensure the safe operation of production;

7. Responsible for discovering, proposing and leading the solution of product process problems and technical optimization;

8. Responsible for the investigation of deviations in production, workshop changes, and rectification of potential safety hazards;

9. According to the production tasks and characteristics of the workshop, rationally arrange the fixed posts and personnel, strictly enforce labor discipline, and fully mobilize the enthusiasm of various personnel;

10. Inspect and evaluate the effectiveness of various management work in the workshop, and be responsible for the performance evaluation of all employees in the workshop in accordance with relevant regulations.

11. Responsible for the management of workshop personnel, the implementation of various trainings, and the training of various professionals in the workshop.

Job Requirements:

1. Bachelor degree or above, major in biological preparation, pharmacy or chemistry or related;

2. Three years or more of management experience in preparation production workshops, working experience in large preparation companies is preferred;

3. Familiar with the preparation production process, GMP regulations and relevant laws and regulations on safe production and fire protection;

4. Be serious, responsible and responsible, with strong execution, good organization and coordination skills and communication skills.

Job Responsibilities:

1. Responsible for drafting and revising relevant GMP documents including process procedures, batch production records, standard operating procedures, etc.;

2. Responsible for guiding the workshop to perform process verification, and solve the problems that occur during the process verification.

3. Supervise the implementation of production in accordance with approved production instructions, process regulations and standard operating procedures;

4. Review relevant records in the production process;

5. Responsible for organizing GMP and standard operating procedures and production technology training for production personnel;

6. Assist in the investigation and handling of quality abnormalities such as process deviations during the production process;

7. Assist the workshop director to complete the production tasks in a timely, safe, quality and quantity manner in accordance with the production instructions and post standard operating procedures.

8. Assist R&D to complete the production conversion work of products;

9. Assist the workshop director to do a good job in the management of workshop personnel and daily affairs.

Job Requirements:

1. Bachelor degree or above, major in pharmaceutical preparation, pharmacy, pharmacy or pharmacy-related;

2. More than one year of preparation technology research or production technology work experience, and those with excellent conditions can relax to fresh graduates;

3. Possess the ability of preparation experiment operation, and be familiar with commonly used preparation equipment;

4. Familiar with relevant laws and regulations on preparations research and development at home and abroad, and systematic GMP knowledge is preferred.

5. Be honest and reliable, work conscientious and responsible, proactive, dedicated to work, and possess team spirit.

Job Responsibilities:

1. Responsible for on-site supervision and inspection of the company's preparation production workshop to ensure that personnel perform relevant operations according to regulations;

2. Responsible for organizing the revision, maintenance and updating of verification related documents, as well as other necessary QA documents, and conduct training and supervision;

3. Responsible for carrying out related quality management activities, such as tracking and handling issues such as deviations, changes, complaints, OOS, etc.;

4. Routine verification management and work arrangements, including verification cycle planning and maintenance, verification plan/verification report organization and review, verification data processing and exception handling, verification review report organization and drafting, verification document management, etc.;

5. Assist in the approval of GMP-related equipment purchase applications and engineering transformation applications;

6. Assist in completing quality-related work in the design of new projects;

7. Complete various tasks assigned by the leader.

job requirements:

1. College degree or above, major in pharmaceutical preparation, pharmacy or pharmaceutical engineering;

2. More than one year of work experience in preparation-related positions (on-site QA, production management, etc.) is preferred. Excellent graduates can also be considered.

3. Be serious and meticulous, have a strong sense of responsibility, have good communication and coordination skills and teamwork skills