Job responsibilities：
1. Assist the manager of the quality control department to transfer and build a QC analysis platform to ensure the safety and standard operation of the laboratory, analysis methods and record management meet the requirements of pharmacopoeia and GMP, and meet the requirements of data integrity and reliability;
2. Responsible for formulating/revising/improving the quality standards and analysis methods for testing bacteria and viruses, raw materials, packaging materials, process water, intermediates, stock solutions, semi-finished products and finished products in accordance with the pharmacopoeia, registration standards, regulations and company requirements;
3. Assist in formulating/revising/improving the management methods of inspection equipment, reagents, test solutions, standard products (or reference products), culture medium, etc., and implement and implement them daily;
4. Maintain the QC quality system, be responsible for the laboratory document management, be responsible for the review of the inspection report, and ensure the correctness, compliance and timeliness of the inspection report issued by the inspector;
5. Responsible for the confirmation/verification of laboratory related facilities, equipment and instruments, and the transfer and verification of analysis methods;
6. Responsible for laboratory deviation, OOS/OOT, change management;
7. Responsible for stability inspection, sample retention, commissioned inspection and other management work;
8. Actively complete other tasks assigned.
Job requirements:
1. Major in pharmaceutical analysis, biopharmaceuticals, chemistry or related, bachelor degree or above;
2. More than three years of bachelor's degree and more than two years of master's degree in QC work experience in biopharmaceutical production enterprises;
3. Familiar with the relevant laws and regulations and guiding principles of the biomedical industry, master the knowledge of drug quality inspection, familiar with various routine operating procedures of biological drug quality control and drug inspection, and be able to find and solve QC test related problems in a timely and effective manner;
4. Familiar with biopharmaceutical biochemical, instrument and activity inspection operations, familiar with the operation of biopharmaceutical testing instruments such as high performance liquid chromatography, capillary electrophoresis, microplate reader and other common instruments, and be able to conduct inspection guidance and training for QC personnel;
5. Rigorous work, serious and responsible, proactive, with strong analysis and judgment, organization and coordination, and problem-solving skills, with good communication skills, coordination and problem-solving skills, and team management skills;
6. Experience in registration and application of biological products, commercial production experience is preferred.
Job responsibilities：
1. According to the corresponding research plan, perform the transfer, verification and inspection of protein drug instrumental analysis methods, complete experimental records and summary reports, etc. The main content of the experiment includes: liquid phase, capillary electrophoresis and other inspection items;
2. Participate in the formulation and revision of inspection operating procedures and related instruments and equipment operating procedures;
3. Responsible for the daily inspection of samples, filling in test records, summary analysis of experimental data, and participating in the investigation of abnormal data such as OOS and OOT;
4. Routine maintenance, calibration and verification of inspection instruments;
5. Actively complete other tasks assigned.
Job requirements:
1. College degree or above in biochemistry, analytical chemistry, pharmaceutical analysis and other related majors, and more than 2 years of relevant work experience in protein pharmaceutical instrument analysis;
2. Familiar with the use and maintenance of high performance liquid chromatography and capillary electrophoresis, familiar with detection methods such as SEC, RP, CEX, glycan, peptide map, CE-SDS, iCIEF, etc.;
3. Serious and meticulous, good at thinking, responsible, good communication skills and execution ability;
4. Familiar with common office software;
5. Working experience in GMP QC laboratory is preferred.
Job responsibilities：
1. Participate in the construction of cell culture workshops, including process rationality verification, production scale and production equipment selection, etc.
2. Responsible for the URS drafting and review of the cell culture plant and related rooms and equipment in each workshop, closely cooperating with the design company and construction company, providing relevant professional technical parameters, answering professional questions; confirming that the construction drawings meet the technical specifications, and checking the clean area installation and equipment The installation and other processes are reasonably compliant.
3. Cooperate with QA and Equipment Engineering Department to complete process equipment procurement, including process equipment selection research, URS drafting, bidding, contract, DQ, FAT/SAT, acceptance, handover and other project life cycle management;
4. Participate in equipment installation, commissioning and 3Q verification in accordance with GMP regulations and quality management documents, and cooperate to complete the drafting or review of relevant documents.
5. After reaching the production capacity, be responsible for the daily production and equipment maintenance of the workshop, assist in the implementation of technology transfer, and compile the SOP and record documents related to the cell culture process. Complete process confirmation and production in the newly built GMP production workshop.
6. Participate in the production of new projects.
7. Other related matters arranged by the company.
job requirements：
1. Bachelor degree or above, major in bioengineering, biotechnology, etc., with experience in large-scale cell culture.
2. More than 3 years of working experience in biopharmaceutical cell culture workshop (GMP).
3. Familiar with equipment verification, cleaning verification and process verification and other related work
4. Have a good team spirit.
5. Experience in new projects of pharmaceutical factories/workshops is preferred.
Job responsibilities：
1. According to the corresponding research plan, carry out the transfer, verification and inspection of biological product analysis methods, complete experimental records and summary reports, etc. The main contents of the experiment include: biological activity, ELISA, PCR and other check items;
2. Participate in the formulation and revision of inspection operating procedures and related instruments and equipment operating procedures;
3. Responsible for the establishment and management of cell banks for inspection in accordance with GMP requirements;
4. Responsible for daily inspection of samples, filling in test records, summary analysis of experimental data, and participating in the investigation of abnormal data such as OOS and OOT;
5. Routine maintenance, calibration and verification of inspection instruments;
6. Actively complete other tasks assigned.
job requirements：
1. Pharmaceutical analysis, biology and other related majors, college degree or above, more than 2 years of relevant work experience;
2. Familiar with the activity detection of biomacromolecule drugs, have certain cell culture work experience, and master conventional cell culture techniques (sterile operation, cell culture, counting, passage, cryopreservation, etc.);
3. Serious and meticulous, good at thinking, responsible, good communication skills and execution ability;
4. Familiar with common office software;
5. Working experience in GMP QC laboratory is preferred.
Job responsibilities：
1. Carry out microbiological related testing (BET, MLT, sterility testing, mycoplasma testing, etc.) of the original, auxiliary, package, finished and intermediate products, and ensure the compliance of the testing process and records, and the accuracy of the results;
2. In accordance with GMP requirements, be responsible for the establishment and management of the bacterial strain library for inspection, maintain the laboratory strain/consumable stock, and ensure the compliance of bacterial strain and consumable management;
3. Summary and analysis of experimental data, and participate in the investigation of abnormal data such as OOS and OOT;
4. Routine maintenance, calibration and verification of inspection instruments;
5. Actively complete other tasks assigned.
job requirements：
1. College degree or above in biochemistry, analytical chemistry, pharmaceutical analysis and other related majors, and more than 2 years of relevant work experience in microbial analysis;
2. Familiar with aseptic operation and microbiological testing;
3. Serious and meticulous, good at thinking, responsible, good communication skills and execution ability;
4. Familiar with common office software;
5. Working experience in GMP QC laboratory is preferred.
Job responsibilities：
1. Compile and revise GMP-related documents such as operating SOPs and batch production records in accordance with the production process.
2. According to the production plan, carry out the procurement plan submission, material acceptance, material application, material storage and return of the production materials.
3. Carry out production activities in accordance with the production plan, including document preparation, material preparation, solution preparation, production execution (preparation filling, freeze-drying production, etc.), verification and other related work.
4. Preparations related to preparation production in GMP workshop, including material preparation, buffer preparation, equipment cleaning, etc.; responsible for the cleaning and sterilization of equipment in the production area; cleaning and sterilization of clean clothes.
5. Perform production operations in strict accordance with batch production records and related SOP requirements; complete the tasks in an effective and timely manner; ensure timely, true and standardized completion of relevant records; any abnormalities and errors in the production process must be reported in time.
6. Carry out the management, cleaning and maintenance of the equipment; carry out the cleaning of the relevant areas in the workshop.
job requirements：
1. College degree or above in pharmaceutical related majors, at least one year of relevant work experience in sterile preparation production.
2. Experience in the production and equipment use of cillin bottle water injection and freeze-dried powder injection is preferred; familiar with the operation of the sterilizer.
3. Have strong stress resistance and team spirit, strong sense of responsibility and strong execution.
4. Proficiency in using common office software such as OFFICE.
Job responsibilities：
1. According to the company's production plan, organize the protein preparation process to be carried out in an orderly manner, and coordinate the relevant departments to ensure that the target is achieved as planned.
2. Ensure that the production behavior of the protein preparation process is carried out in full accordance with the provisions of the production management documents to ensure that the production quality meets GMP standards.
3. Responsible for organizing the preparation, revision, issuance, and supervision of the process regulations, post operation regulations, equipment operation regulations, production batch records, and various forms used for recording to ensure that the contents of the documents are consistent with the production.
4. Responsible for the review and approval of related documents, records, and quality control procedures for the protein preparation process.
5. Responsible for organizing the protein preparation process operations in accordance with the standard operating procedures, and fill in the records according to the specifications and file them in time
6. Responsible for process reception, confirmation, amplification and verification, and complete commercial production after process transfer.
7. Responsible for organizing the improvement of this process technology and equipment, participating in the selection of process equipment, data writing, procurement, installation, commissioning, verification, etc., to ensure that the improvement is compliant and carried out in an orderly manner;
8. Responsible for the management, cleaning and maintenance of the equipment in this process, and the cleaning of related areas.
9. Maintain good communication and cooperation with the cell culture, protein purification process and engineering, quality, logistics and other departments of the production department.
job requirements：
1. Bachelor degree or above in bioengineering and pharmaceutical related majors.
2. Bachelor's degree or more, and master's degree or more than three years of production experience in Xilin bottle water injection and freeze-dried powder injection, team management experience is preferred.
3. Familiar with the relevant regulatory requirements of GMP in the field of biopharmaceuticals, and be able to write GMP-related documents such as SOP and batch records.
4. Have strong anti-stress ability and team spirit, strong sense of responsibility and strong execution ability.
5. Experience in registration and application of biological products, and experience in commercial production is preferred.
Job responsibilities：
1 Responsible for preparation production management activities. According to the company's production plan, organize the workshop to carry out production in an orderly manner, and do a good job in coordination with relevant departments to ensure that the target is achieved as planned.
2. Ensure that the production behavior of the preparation workshop is carried out in full accordance with the production management documents and ensure that the production quality meets GMP standards.
3. Responsible for organizing the preparation, revision, issuance and supervision of the process regulations, post operation regulations, equipment operation regulations, production batch records and various forms used for records, to ensure that the contents of the documents are consistent with the production.
4. Responsible for the review and approval of relevant documents, records and quality control procedures of the preparation workshop.
5. Responsible for organizing the preparation process operations in accordance with the standard operating procedures, and fill in the records according to the specifications and file them in time.
6. Responsible for process reception, confirmation, amplification and verification, and complete commercial production after process transfer.
7. Responsible for organizing the improvement of the technology and equipment of the workshop, organizing and participating in the selection of process equipment, data writing, procurement, installation, commissioning, verification, etc., to ensure 8. Improve compliance and orderly progress; conduct equipment management and cleaning And maintenance; clean the relevant areas in the workshop.
job requirements：
1. Bachelor degree or above in biopharmaceutical related majors.
2. Engaged in preparation production for more than 5 years, and no less than 3 years of team management experience.
3. Familiar with the relevant regulations and requirements of GMP in the field of biopharmaceuticals.
Job responsibilities：
1. According to the production process, compile and revise GMP related documents such as SOP and batch production records.
2. According to the production plan, carry out the procurement plan submission, material acceptance, material application, material storage and return of the production materials.
3. Carry out production activities in accordance with the production plan, including document preparation, material preparation, solution preparation, production execution (protein affinity chromatography, protein ion exchange chromatography, virus removal filtration, ultrafiltration, etc.), verification and other related work.
4. Preparations related to purification production in the GMP workshop, including the preparation of materials during the production process, buffer preparation, equipment cleaning, etc.; cleaning and sterilization of appliances in the production area; cleaning and sterilization of clean clothes.
5. Perform production operations in strict accordance with batch production records and related SOP requirements; complete the tasks in an effective and timely manner; ensure timely, true and standardized completion of relevant records; any abnormalities and errors in the production process must be reported in time.
6. Carry out the management, cleaning and maintenance of the equipment; carry out the cleaning of the relevant areas in the workshop.
job requirements：
1. College degree or above in pharmaceutical related majors, at least one year of relevant work experience.
2. Relevant experience in the use of downstream production equipment such as automatic chromatography equipment AKTA Process, filtration equipment, ultrafiltration equipment is preferred; familiar with the operation of the sterilization cabinet.
3. Proficiency in buffer preparation using disposable dispensing bags from mainstream manufacturers on the market; understand basic knowledge of protein chromatography or membrane filtration
4. Have strong anti-stress ability and team spirit, strong sense of responsibility and strong execution ability.
5. Proficiency in using common office software such as OFFICE.
Job responsibilities：
1. Participate in the construction of the purification process line of the plant, including the rationality check of the process flow, the production scale and the selection of production equipment, etc.
2. Responsible for the URS drafting and review of the cell culture plant and related rooms and equipment in each workshop, closely cooperating with design companies and construction companies, providing relevant professional technical parameters, and answering professional questions;
3. Cooperate with QA and Equipment Engineering Department to complete process equipment procurement, including process equipment selection research, URS drafting, bidding, contract, DQ, FAT/SAT, acceptance, handover and other project life cycle management;
4. Participate in equipment installation, commissioning and 3Q verification in accordance with GMP regulations and quality management documents, and cooperate to complete the drafting or review of relevant documents.
5. After reaching the production capacity, be responsible for the daily production and equipment maintenance of the workshop, assist in the implementation of technology transfer, and compile the SOP and record documents related to the purification process. Complete process confirmation and production in the newly built GMP production workshop.
6. Participate in the production of new projects.
7. Other related matters arranged by the company.
job requirements：
1. Bachelor degree or above, major in biology, chemistry, pharmacy, etc.
2. More than 3 years of working experience in biopharmaceutical purification workshop (GMP).
3. Familiar with equipment verification, cleaning verification and process verification and other related work.
4. Have a good team spirit.
5. Experience in new projects of pharmaceutical factories/workshops is preferred.
Job responsibilities：
1. According to the company's production plan, the tissue protein purification process is carried out in an orderly manner, and the relevant departments are coordinated to ensure that the target is achieved as planned.
2. Ensure that the production behavior of the protein purification process is carried out in full accordance with the provisions of the production management documents to ensure that the production quality meets GMP standards.
3. Responsible for organizing the preparation, revision, issuance, and supervision of the process regulations, post operation regulations, equipment operation regulations, production batch records, and various forms used for records to ensure that the content of the documents is consistent with the production.
4. Responsible for the review and approval of relevant documents, records, and quality control procedures for the protein purification process.
5. Responsible for organizing the protein purification process operations in accordance with the standard operating procedures, and fill in the records according to the specifications and file them in time.
6. Responsible for process reception, confirmation, amplification and verification, and complete commercial production after process transfer.
7. Responsible for organizing the improvement of this process technology and equipment, participating in process equipment selection, data writing, procurement, installation, debugging, verification, etc., to ensure that the improvement is in compliance and orderly;
8. Responsible for the management, cleaning and maintenance of the equipment in this process, and the cleaning of related areas.
9. Maintain good communication and cooperation with the cell culture, technology transfer process and engineering, quality, logistics and other departments of the production department.
job requirements：
1. Bachelor degree or above in biopharmaceutical related majors.
2. At least five years of bachelor degree and three years of master degree in recombinant protein purification work experience, team management experience is preferred.
3. Familiar with the relevant regulatory requirements of GMP in the field of biopharmaceuticals, and be able to write GMP-related documents such as SOP and batch records.
4. Have strong anti-stress ability and team spirit, strong sense of responsibility and strong execution ability.
5. Experience in registration and application of biological products, and experience in commercial production is preferred.
Job responsibilities：
1. Compile and revise GMP-related documents such as operating SOPs and batch production records in accordance with the production process.
2. According to the production plan, carry out the procurement plan submission, material acceptance, material application, material storage and return of the production materials.
3. Carry out production activities in accordance with the production plan, including document preparation, material preparation, solution preparation, production execution (cell recovery, expansion, bioreactor production, clarification and filtration, etc.), verification and other related work.
4. Preparations related to cell culture production in the GMP workshop, including material preparation, culture medium preparation, and equipment cleaning during the production process; cleaning and sterilization of appliances in the production area; cleaning and sterilization of clean clothes.
5. Perform production operations in strict accordance with batch production records and related SOP requirements; complete the tasks in an effective and timely manner; ensure timely, true and standardized completion of relevant records; any abnormalities and errors in the production process must be reported in time.
6. Carry out the management, cleaning and maintenance of the equipment; carry out the cleaning of the relevant areas in the workshop.
job requirements：
1. College degree or above in biopharmaceutical related majors, with at least one year of relevant work experience.
2. Familiar with animal cell culture process and have good aseptic operation skills.
3. Proficiency in the use of production and quality control analysis equipment such as disposable bioreactors, filtration equipment, biological safety cabinets, cell counters, and multifunctional biochemical analyzers with a scale of 50L or more; experience in using WAVE/STR bioreactors is preferred.
4. Have strong anti-stress ability and team spirit, strong sense of responsibility and strong execution ability.
5. Proficiency in using common office software such as OFFICE.
Job responsibilities：
1. Participate in the construction of cell culture workshops, including process rationality verification, production scale and production equipment selection, etc.
2. Responsible for the URS drafting and review of the cell culture plant and related rooms and equipment in each workshop, closely cooperating with the design company and construction company, providing relevant professional technical parameters, answering professional questions; confirming that the construction drawings meet the technical specifications, and checking the clean area installation and equipment The installation and other processes are reasonably compliant.
3. Cooperate with QA and Equipment Engineering Department to complete process equipment procurement, including process equipment selection research, URS drafting, bidding, contract, DQ, FAT/SAT, acceptance, handover and other project life cycle management;
4. Participate in equipment installation, commissioning and 3Q verification in accordance with GMP regulations and quality management documents, and cooperate to complete the drafting or review of relevant documents.
5. After reaching the production capacity, be responsible for the daily production and equipment maintenance of the workshop, assist in the implementation of technology transfer, and compile the SOP and record documents related to the cell culture process. Complete process confirmation and production in the newly built GMP production workshop.
6. Participate in the production of new projects.
7. Other related matters arranged by the company.
job requirements：
1. Bachelor degree or above, major in bioengineering, biotechnology, etc., with experience in large-scale cell culture.
2. More than 3 years of working experience in biopharmaceutical cell culture workshop (GMP).
3. Familiar with equipment verification, cleaning verification and process verification and other related work
4. Have a good team spirit.
5. Experience in new projects of pharmaceutical factories/workshops is preferred.
Job responsibilities：
1. According to the company's production plan, the tissue cell culture process is carried out in an orderly manner, and the relevant departments are coordinated to ensure that the target is achieved as planned.
2. Ensure that the production behavior of the cell culture process is carried out in full accordance with the provisions of the production management documents to ensure that the production quality meets GMP standards.
3. Responsible for organizing the preparation, revision, issuance, and supervision of the process regulations, post operation regulations, equipment operation regulations, production batch records, and various forms used for records to ensure that the content of the documents is consistent with the production.
4. Responsible for the review and approval of relevant documents, records, and quality control procedures for the cell culture process.
5. Responsible for organizing cell culture process operations in accordance with standard operating procedures, and filling in records according to specifications and filing in time.
6. Responsible for process reception, confirmation, amplification and verification, and complete commercial production after process transfer.
7. Responsible for organizing the improvement of this process technology and equipment, participating in process equipment selection, data writing, procurement, installation, debugging, verification, etc., to ensure that the improvement is in compliance and orderly;
8. Responsible for the management, cleaning and maintenance of the equipment in this process, and the cleaning of related areas.
9. Maintain good communication and cooperation with the purification, technology transfer process and engineering, quality, logistics and other departments of the production department
job requirements：
1. Bachelor degree or above in biopharmaceutical related majors.
2. At least five years of undergraduate degree and three years of master’s degree in large-scale cell culture work experience, team management experience is preferred.
3. Familiar with the relevant regulatory requirements of GMP in the field of biopharmaceuticals, and be able to write GMP-related documents such as SOP and batch records.
4. Have strong anti-stress ability and team spirit, strong sense of responsibility and strong execution ability.
5. Experience in registration and application of biological products, and experience in commercial production is preferred.
Job responsibilities：
1. Participate in the construction of a 10-ton microbial fermentation plant, including process rationality verification, production equipment selection, etc.
2. Responsible for the URS drafting and review of the microbial fermentation plant and related rooms and equipment in each workshop, closely cooperating with the design company and construction company, providing relevant professional technical parameters, answering professional questions; confirming that the construction drawings meet the technical specifications, and checking the clean area installation and equipment The installation and other processes are reasonably compliant.
3. Cooperate with QA and Equipment Engineering Department to complete process equipment procurement, including process equipment selection research, URS drafting, bidding, contract, DQ, FAT/SAT, acceptance, handover and other project life cycle management;
4. Participate in equipment installation, commissioning and 3Q verification in accordance with GMP regulations and quality management documents, and cooperate to complete the drafting or review of relevant documents.
5. After reaching production, be responsible for the daily production and equipment maintenance of the workshop, assist in the implementation of technology transfer, and compile SOPs and record documents related to the fermentation process. Complete process confirmation and production in the newly built GMP production workshop.
6. Participate in the production of new projects.
7. Other related matters arranged by the company.
job requirements：
1. Bachelor degree or above, major in bioengineering and microbiology
2. More than 3 years of working experience in biopharmaceutical microbial fermentation workshop (GMP).
3. Familiar with equipment verification, cleaning verification and process verification and other related work
4. Have a good team spirit.
5. Experience in new projects of pharmaceutical factories/workshops is preferred.
Job responsibilities：
1. Participate in the selection and investigation of public engineering equipment and process equipment, URS drafting, bidding, contract, DQ, FAT/SAT, acceptance, handover and other project life cycle management during plant construction;
2. Participate in equipment installation, commissioning and 3Q verification in accordance with GMP regulations and quality management documents;
3. Establish and update equipment preventive maintenance procedures, plan and implement preventive maintenance, corrective maintenance and emergency maintenance of production equipment to ensure the normal operation of the equipment; urgently organize the maintenance of production equipment to ensure normal production;
4. Manage equipment suppliers and maintenance suppliers, and organize acceptance after purchase;
5. Responsible for the compilation, revision and specific implementation of equipment related documents, establish and maintain equipment archives;
6. Responsible for the daily use and maintenance training of the equipment in various departments to ensure the normal use of the equipment;
7. Responsible for the procurement, warehousing, requisition and inventory management of spare parts;
8. Assist in handling equipment-related deviations;
9. Comply with the company's rules and regulations to summarize and report and complete other tasks arranged by the superior.
job requirements：
1. Education background: Bachelor degree or above.
2. Major: Mechanical, electrical or engineering major.
3. More than five years of experience in operation, maintenance and management of equipment and facilities in pharmaceutical companies, familiar with the equipment and facilities of biomedical production lines, such as washing, drying, filling and rolling equipment, freeze dryers, etc., able to independently draft relevant documents, and proficient in the use of CAD drawing software and Office software.
4. Has a strong ability to analyze and eliminate equipment failure hidden dangers.
5. Good inter-departmental communication and coordination skills.
6. Received training on knowledge including pharmaceutical production GMP, quality and environmental system standards, safety, and environmental protection.
7. Experience in new projects of pharmaceutical factories/workshops is preferred.
| 30000-40000 |
Job responsibilities：
1. Responsible for the construction of the system document framework, document drafting and review, and effective work during the preparation of the plant.
2. New project public engineering system, storage system and other related work, including but not limited to equipment URS audit, DQ, FAT, SAT, IQ, OQ, PQ, etc., as well as changes, deviations, risk assessments, etc. during the implementation of new projects Quality activities.
3. Implement the management work of the quality system operation, including product process optimization, implementation verification, process confirmation, deviation investigation, product quality improvement and promotion.
4. Assist to complete the analysis and resolution of quality problems in the process of plant construction, identify system hidden dangers and improvement opportunities, and seek improvement methods to optimize product quality monitoring.
5. Complete other tasks assigned by the leader.
job requirements：
1. Major in pharmaceutical analysis, pharmacy, biology or related, bachelor degree or above.
2. More than 5 years of working experience in a biopharmaceutical factory, involving product lines including stock solutions and sterile preparations.
3. Familiar with the production process of biological products, drug registration management methods, domestic and foreign GMP, ICH guidelines or have relevant drug production experience; proficient in quality management tools (such as risk assessment) and methods of use.
4. Familiar with cleaning verification, analytical method verification, process verification and other related knowledge.
5. Have good coordination and communication skills, independent thinking and analysis skills.
6. Have the spirit of teamwork and a sense of work responsibility.
7. Experience in new projects of pharmaceutical factories/workshops is preferred.
Job responsibilities：
1. Responsible for the design, demonstration, construction and operation of new factory safety facilities, environmental protection facilities, and occupational health facilities;
2. Responsible for the safety and environmental protection management of the construction site;
3. Responsible for establishing a safety and environmental protection management system, and ensuring that the system operates in a scientific, effective and efficient manner;
4. Organize the implementation of various safety activities; urge all departments to conduct safety education within the department, and assist all departments in formulating safety activity plans;
5. Responsible for the comprehensive management of company safety, environmental protection (sewage treatment facilities), sanitary equipment and facilities, and coordinate with relevant departments to do its maintenance, repair, and inspection management;
6. Responsible for the company's hazardous chemicals management, and coordinate the company's liquid waste and solid waste management;
7. Responsible for the "three simultaneous" work of new construction, expansion and reconstruction and the EHS audit of overhaul and technical renovation projects to make them meet the EHS technical requirements;
8. In-depth on-site supervision and inspection from time to time, supervise and assist in solving related hidden dangers, and correct illegal operations.
Job requirements:
1. Bachelor degree or above, major in environmental engineering, safety engineering, etc.;
2. Three years of experience in environmental safety or similar positions in pharmaceutical companies, and hold a national registered safety engineer qualification certificate;
3. Familiar with national and local safety and environmental protection, occupational health laws and regulations, and have good practical experience in safety management, environmental protection management, and operation of environmental protection facilities;
4. Work actively, enthusiastically, meticulously and seriously, with a strong sense of responsibility.
Job responsibilities：
1. Participate in the electrical planning of plant facilities, the life cycle management of bidding, design, construction, acceptance, and handover of public engineering equipment, pipelines, fire protection, water supply and drainage during the construction of the plant.
2. Responsible for the preparation and implementation of procurement and bidding in new construction and reconstruction projects, the review of design drawings, the review and collection of professional completed drawings.
3. Responsible for the company's electrical system fault management, and provide timely solutions to the faults reported by various departments.
4. Develop annual and monthly maintenance plans for the company's plant facilities (building management system BMS), HVAC system, and power distribution system.
5. Ensure the normal operation of the plant's electrical, gas, and HVAC equipment, collect and analyze data on the equipment in the responsible area on time, and communicate the technical status of the equipment with relevant personnel/department personnel in a timely manner.
6. Responsible for regional facilities and equipment management, inspections and technical transformation, plan maintenance, and reduce fault maintenance.
job requirements：
1. Education background: college degree or above.
2. Major: Mechanical, electrical or engineering major.
3. Work experience: more than five years of work experience, more than three years of experience in electromechanical related operation management or project execution in a pharmaceutical factory.
4. Familiar with relevant theoretical knowledge of equipment, water, electricity, heating, steam, gas, etc.
5. Familiar with the maintenance operation process of equipment and facilities in the pharmaceutical industry, such as HVAC and electrical systems.
6. Proficient in strong current and weak current theory, strong practical operation ability, should have a strong current qualification certificate.
7. Knowledge skills and level requirements: be able to use CAD drawing software and Office software proficiently.
8. Good communication skills and cooperative spirit.
9. Experience in new projects of pharmaceutical factories/workshops is preferred.
Job responsibilities：
1. Establish a human resource management system, process, and system to improve the operational efficiency of the human resource system;
2. Based on the company's strategy and business development requirements, go deep into the business department, proactively obtain the demands of the business department's human resources work, and provide and implement effective solutions in recruitment, training, performance appraisal, salary, employee relations, etc.;
3. Conduct a talent inventory of business departments, pay attention to the cultivation, development and promotion of key talents, help business departments build talent echelons, and promote organization and talent development;
4. Actively interact with management and employees, communicate effectively in multiple forms to ensure the effective transmission of internal information, and gradually establish a benign internal communication mechanism;
5. Promote the continuous improvement of the company's training management system based on the needs of business departments;
6. Promote the construction of the company's performance management system, promote performance management and continuous improvement with performance as the guidance and performance improvement as the goal, to help employees improve work effectiveness and accelerate personal growth;
7. Carry out the construction of the company's cultural system and brand building, create a positive organizational atmosphere, and ensure the sustained and healthy growth of the organization.
job requirements：
1. Bachelor degree or above, more than 8 years of human resources work experience, HR experience in the pharmaceutical industry is preferred;
2. Understand the work of each module of human resources, and be proficient in training, performance and employee relations modules;
3. Strong interpersonal understanding, communication and coordination skills, and good at integrating resources to drive goals;
4. Strong sense of responsibility, strong resistance to pressure, and the ability to solve complex problems;
Job responsibilities：
1. Responsible for the preparation and construction of the new plant, connect the company's headquarters with various local tasks, deal with all kinds of emergencies in a timely manner, and ensure the smooth progress of the project;
2. Coordinate and manage the overall operation of the new factory's production, including workshop organization and scheduling, production management, cost control, etc.;
3. Strictly control the production process according to GMP requirements to ensure product quality;
4. Coordinate and manage the equipment, facilities, purchases, warehouses, etc. of the new factory to ensure normal production, and to undertake finished product shipment tasks and provide sales support services;
5. Cooperate with the quality department, and do a good job of GMP compliance management of the department under the company's quality management policies and strategies.
job requirements：
1. College degree or above in medicine, pharmacy, mechanical equipment and other related majors;
2. Familiar with the domestic and foreign pharmaceutical industry and related policies and regulations, and have more than 10 years of production management experience in large and medium-sized pharmaceutical factories, and experience in biological fermentation is preferred;
3. Familiar with all aspects of production management in pharmaceutical factories, and have experience in preparation of new factories and new version of GMP certification;
4. Have the ability to plan, organize, coordinate and communicate, and have a strong sense of responsibility;
5. Strong resistance to pressure, able to adapt to business trips.