Jobs
Talent concept
The talent concept is the guiding ideology and values for enterprises to value, cherish, develop, utilize, retain, and enhance talents.
Our company aims to seek development, strengthen strength, expand scale, and create a brand. Adhering to the corporate philosophy of "technological innovation, people-oriented", we warmly welcome universities, research institutes, and pharmaceutical production enterprises to join forces with our company, complement each other's advantages, and establish a win-win cooperation relationship.
Mission
Vision
Market position
Huafang Pharmaceutical
· Talent concept
People oriented, talent is the capital of enterprises.
Recruitment positions
R&D
1. Bachelor degree or above;
2. Major in organic chemistry, Pharmaceutical Chemistry, Chemistry, etc., CET-4 or above;
3. More than 4 years bachelor's degree and more than 2 years master's practical working experience in drug synthesis;
4. Experience in pilot scale up;
5, with rich chemical synthesis ability, can independently design synthesis route;
6. Proficient in foreign language retrieval and reading;
7, with the ability to analyze H-NMR, MS, IR, powder diffraction and other analytical spectrum;
8. Experience in drug registration and application is preferred;
1. Bachelor degree or above in organic chemistry or pharmaceutical chemistry or related major;
2. Master's degree holders should have more than 1 year working experience in this position, and bachelor's degree holders should have more than 2 years working experience;
3. Completed literature review independently, and completed preliminary design of compound synthesis route according to literature;
4. Be familiar with the operation of organic synthesis unit and complete chemical reaction skillfully;
5. Complete the experiment records and reports clearly and completely;
6. Good sense of responsibility and teamwork spirit, and good thinking habits; Good coordination and management ability;
7, with the unity of colleagues, open-minded quality; Have a strong sense of collective honor, and good communication skills;
8. Steadfast, hardworking, dedicated and enterprising work style.
1. Participate in the company's test projects;
2. Sorted out statistical analysis of test data, wrote reports, and sorted out application materials according to requirements;
3. Complete the tasks assigned by superiors.
Qualifications:
1. Bachelor degree or above in pharmacy, pharmaceutical analysis or quality analysis;
2. Rich theoretical and practical experience in the field of quality analysis, skilled in the operation of liquid and gas equal analysis equipment, capable of product research and development;
3. Candidates who have undertaken research projects in related fields and published research papers in relevant professional journals at home and abroad are preferred;
4. Have certain interpersonal communication and coordination ability, high written expression ability, calm personality, practical work, studious;
5, Good communication and cooperation skills, good team spirit.
1. Bachelor degree or above in pharmaceutical analysis or related major, with more than 1 year working experience 2. Proficient in operating LC-MS/MS and other analytical instruments, proficient in the development of LC-MS/MS analytical methods for drug concentration detection in ***, familiar with the requirements for verification of biological analytical methods 3. Have a certain understanding of pharmacokinetics, and master the guiding principles and regulations related to pharmacokinetic research. 4, with good learning ability and practical ability, animal experiment, sample processing or BE evaluation experience is preferred 5. Proficient in Microsoft Excel worksheets and Microsoft Word documents. 6, Have a good sense of responsibility, positive team spirit
1. Candidates with bachelor's degree and engaged in drug research for more than three years, or candidates with postgraduate degree and engaged in drug research for more than one year;
2. Professional knowledge related to pharmacy, pharmacology or analysis and testing, independently undertaken project research and development;
3, have a certain level of English and computer operation knowledge;
4. Have a certain literature retrieval ability, independent or organized drug researchers are preferred;
5. Familiar with relevant knowledge of drug research (such as drug administration and regulations, drug registration knowledge);
6. Good sense of responsibility and teamwork spirit, and good thinking habits; Good coordination and management ability;
7, with the unity of colleagues, open-minded quality; Have a strong sense of collective honor, and good communication skills;
8. Steadfast, hardworking, dedicated and enterprising work style.
1, skilled use of silica gel, gel, reverse phase, preparation chromatography and other separation means 2. Proficient in chemidrow, MestReNova and other software 3. Proficient in structural analysis methods of compounds such as H spectrum and C spectrum 4. Proficient in reading professional English, capable of document retrieval and corresponding information query 5, PhD or more than 3 years of work in natural medicine chemistry of master's degree is preferred Age requirement: 25-45 years old
1. Responsible for the management of the R&D process of various projects in the Pharmacology Department, controlling all links in the R&D process, coordinating the project process and the cooperation work of various departments in the Pharmacology Department.
2. Responsible for designing pharmacology related topics and leading the team to carry out pharmacology related experimental research.
3. Responsible for writing relevant approval materials of pharmacological and toxicological experiments, etc.
Qualifications:
1. Ph. D. degree or more than 3 years working experience in pharmacology, pharmacokinetics, epidemiological investigation or biostatistics.
2. Familiar with pharmacology and toxicology related experimental methods, able to independently undertake the construction of in vitro and in vivo drug screening models, activity screening, pharmacokinetics and pharmacodynamics evaluation of new drugs.
3. Have certain project management experience, clear working ideas, and strong ability to analyze and solve problems.
4. Strong writing ability, familiar with new drug registration and patent application process.
5. Have good communication skills and collaborative spirit, strong sense of responsibility, and experience in preclinical pharmacology and toxicology and clinical pharmacology evaluation of new drugs is preferred.
Age requirement: 25-50 years old
1. Responsible for GC analysis support and method development during drug research and development, including analysis method development, analysis method transfer, stability study and sample testing.
2. Proficient in GC, GC-MS, IC and other analytical instruments.
3. Familiar with relevant laws, regulations and technical guidelines for drug research and development, familiar with the general process and technical details of new product research and development, quality and stability research.
4. Capable of independently designing quality research programs and stability programs in new drug research and development, and completing related test work.
5. Write experimental records in a timely and standardized manner, and can write application materials independently.
6. Complete project application experience.
7. Responsible for instrument calibration and maintenance, assisting in project management, thematic technology development, laboratory management, etc.
8. Write project reports and other relevant documents.
Job Requirements
1. Major in pharmaceutical analysis, bachelor degree or above, under 35 years old.
2. Major in chemistry, pharmacy or other science and engineering, with GC analysis experience in drug research and development, familiar with GC analysis instruments is preferred.
3. Wrote the project research and proposal report of the project I was responsible for.
4. Make specific development plans and experimental research programs for R&D projects.
5. Write and review the original records and application materials of R&D tests timely, accurately, truly and completely.
6. Complete the "will" and "present test" of the project in charge.
Age requirement: 28-45 years old
Job Description:
1. Skillfully completed the experimental chemical reaction of the project, made a comprehensive analysis and judgment on the results, and completed the experimental report;
2. Complete compound synthesis route design, route selection, process optimization and technical research according to literature;
3. Completed the project work independently, solved the simple problems in the experiment, and completed the experiment records and reports clearly and completely;
4. Be able to operate according to the standards of experimental equipment, use reagents and equipment safely, and comply with the safety system of experimental management;
Qualifications:
1. Master degree or bachelor degree in pharmaceutical chemistry or organic synthesis;
2. Rich experience in organic synthesis laboratory, familiar with all kinds of organic synthesis operations, solid professional knowledge, proficient in experimental operation;
3. Proficient in spectrum analysis, separation and purification technology;
4. CET-6, proficient in literature retrieval and English technical data reading;
5. Honest, rigorous, responsible and self-motivated, love organic synthesis work, team work and innovation spirit, have strong learning ability.
Age requirement: 25-45 years old
Our company relies on the Anhui Academician Workstation, Anhui Postdoctoral Research Workstation, Anhui Key Laboratory, and Municipal Engineering Technology Center to recruit 1-2 PhD candidates. The specific requirements are as follows:
1. Previous doctoral degree graduates (within 3 years after graduation; Under the age of 35) or fresh PhD graduates in 2020;
2. Major in pharmacology (including pharmacokinetics), pharmaceutical preparation, pharmacy, drug synthesis, Chinese pharmacy and other biomedicine related fields;
3. Able to undertake project research independently.
Production category
1. Assist the deputy general manager of production and workshop director to organize production in accordance with GMP requirements, and ensure that production workers strictly follow the production process regulations and post SOP;
2. Assist the director of production management Department to check whether the production workers violate the process discipline according to the process regulations, post SOP and safe operation procedures of machinery and equipment, and be responsible for the accidents caused by the failure to correct the violation of process discipline in time;
3. Timely visit the production site for quality and technical problems, and assist the leaders in charge to properly deal with them;
4. Fill in the production instructions and packaging instructions timely according to the process requirements, and send them to each post after being reviewed by relevant departments;
5. Responsible for the issuance of production process regulations;
6. Accept other temporary tasks assigned by company leaders and department leaders;
7. Experience in GMP workshop management is preferred.
Age requirement: 22-45 years old
1. Responsible for the daily management of the process and engineering equipment of the whole plant, to ensure the normal operation of the equipment, ensure the normal production and routine inspection;
2. Make annual maintenance plan according to production plan and equipment use and maintenance requirements, and organize the implementation;
3. Regularly organize equipment verification, check the condition of production equipment, and timely adjust the maintenance content;
4. According to the actual use and performance of the equipment, apply for and keep the spare parts of the equipment, and prevent and forbid the equipment to stop operation due to the lack of spare parts;
5. Organize and coordinate the selection of process equipment according to the requirements provided by the production and use department, and compile or summarize the URS documents of the equipment;
6. Organized and implemented the unpacking, acceptance, installation and commissioning of process and engineering equipment on site;
7. Organized and took charge of drafting and implementing IQ and OQ documents of process and engineering equipment, and cooperated with the user department to do PQ work of equipment;
8. Organized the preparation of equipment maintenance SOP documents, including revision and training of documents;
9. Establish and improve the relevant management system of process equipment;
10. Complete other tasks arranged.
Qualifications:
1. Education Background: Bachelor degree, major in mechanical, electromechanical, automation and electrical related;
2. Work experience: at least 3 years working experience in equipment maintenance and equipment management in pharmaceutical plant;
3. Working skills: Having certain computer skills, familiar with office software and CAD software, having certain planning, organization, management and control abilities, effectively leading subordinates to complete work.
Age requirement: 25-45 years old
1. Carry out relevant production operations in strict accordance with the production process regulations.
2. Fill in relevant records timely, accurately and truthfully.
3. Responsible for handling the deviation and abnormal situation of the position.
4. Participate in and coordinate production process verification, cleaning verification, equipment verification and other related work.
Job Requirements:
1. College degree or above in medicine, chemical engineering or related field.
2. Down-to-earth, hard-working and self-motivated.
3. Relevant working experience is preferred.
Age requirement: 22-45 years old
1. Responsible for the production scheduling of each workshop, to ensure the balanced production of the whole company and the completion of production instructions. To be responsible for safety and fire control administration within the scope of the department;
2. Participated in the evaluation of suppliers, and was responsible for the inspection and review of procurement of spare parts for production;
3. Mastered the production schedule, coordinated and solved related problems in production, and handled various working relationships within and outside the department. Strengthen site management, monitoring the production environment, health and the whole process of production;
4. Participate in the preparation of technical transformation plan and company development and investment plan; Participate in equipment purchase, project demonstration and engineering verification. Good equipment management;
5. Participated in the GMP assessment of the whole company and the preparation and review of related SOP. Responsible for drafting, formulating and revising product process regulations, health management, equipment management standards and operating regulations, equipment verification schemes, etc. Responsible for the approval and training, the process of the implementation of the process, the implementation of the Specification and product quality;
6. Review and evaluate batch records and batch packaging records, and review the batch production records and batch packaging records that have completed key steps to ensure that all important deviations have been investigated and corrective measures have been taken;
7. Director of pharmaceutical GMP workshop is preferred.
Age requirement: 25-45 years old
Job Description:
1. Responsible for the operation of power and water system equipment and fill in inspection records, maintenance records and related operation records of equipment and facilities timely, accurately and truthfully.
2. Responsible for the repair, maintenance, installation and debugging of production equipment, inspection equipment, living facilities and factory facilities of the whole company.
3. Understand the structure, principle, performance and use of all kinds of equipment and instruments used in the company's production, inspection and life, and be able to maintain and troubleshoot.
4. Guide the operators to use the equipment correctly, so that they can carry out quarterly and annual maintenance of the equipment, often supervise and check the use of the equipment, and understand and master the use status of the equipment.
5. Inspect equipment regularly, solve problems in time and report problems in time.
6. Responsible for completing other temporary work assigned by superior.
Qualifications:
Technical secondary school or above (with good mechanical repair skills, education requirements can be relaxed), major in mechanical and electrical engineering, more than 2 years of working experience in pharmaceutical or food industry equipment maintenance, familiar with oral solid preparation equipment maintenance is preferred.
Quality assurance
1. Lead the whole department to earnestly implement the quality standards and drug quality management rules, and be responsible for the inspection of the company's drug quality.
2. Responsible for organizing the technical and professional learning and assessment of laboratory analysts, organizing the promotion and adoption of advanced analytical methods, and providing scientific basis for improving the quality of drugs.
3. Responsible for whether the laboratory report issued by the department is correct or not.
4. Organize the formulation of quality inspection, sample retention observation, production area health inspection, quality accident analysis, inspection procedures, inspection work system, and check the implementation of all systems at any time.
5. Responsible for organizing the inspection of raw materials, intermediates, products to be inspected and finished products, and issuing inspection reports.
6. Cooperate with QA department and production department to verify production process and other equipment.
7. Familiar with the operation of liquid/gas precision test instrument.
Age requirement: 26-45 years old
1. Be familiar with the properties of various reagents and pay attention to the safety in use. 2. Perform physical and chemical testing of raw and auxiliary materials, packaging materials and finished products of drugs according to SOP, and fill in records in time. 3. Responsible for calibration of laboratory measuring instruments
4. Other work arranged by leader
5. Working experience in pharmaceutical factory/food company is preferred Age requirement: 25-45 years old
1. Responsible for monitoring the whole process of commissioned drug production.
2. Conducted quality audit of entrusted enterprises regularly, followed up audit defects rectification, and evaluated the quality management system of entrusted enterprises.
3. Responsible for the management and audit of drug material suppliers.
4. Responsible for reviewing the batch production records and batch inspection records of commissioned drugs, and assisting in the review of the release of finished products to the market.
5. Responsible for reviewing the verification schemes, process procedures, batch production records and quality standards related to commissioned drugs.
6. Responsible for organizing and dealing with deviations, changes, OOS, complaints and recalls in the production process.
7. Assist in the audit of pharmaceutical printing packaging materials commissioned for production.
8. Responsible for monitoring the verification status of equipment, facilities and environment related to the commissioned production of drugs.
9. Assist the superior to complete the annual quality review and evaluation of commissioned drugs.
10. Assist the superior in the construction and continuous improvement of MAH quality system.
11. Assisted superiors to complete the writing, revision and implementation of MAH quality system documents.
Job Requirements
1, medical related bachelor degree or above, with GMP, drug production supervision and management related professional knowledge.
2. More than 2 years practical experience in drug production and quality management. Experience in drug field monitoring is preferred.
3. Familiar with the production process of oral solid preparation, experience in drug production license certification and compliance inspection is preferred.
4. Have strong communication skills and can adapt to travel around Hefei.
1. Responsible for the testing of raw materials, packaging materials and finished products in pharmaceutical GMP workshop, and fill in records timely;
2. Familiar with the nature of various reagents, master the performance of various instruments, pay attention to the safety in use;
3. Responsible for the maintenance and maintenance of laboratory instruments;
4. Familiar with liquid and gas phase operators are preferred;
Age requirement: 25-45 years old.
1. Responsible for the management of the company's R & D quality system documents.
2. Responsible for the management of MAH related quality documents.
3. Responsible for the establishment and management of supplier files.
4. Responsible for the issuance and archiving of experimental books and auxiliary records.
5. Responsible for the review and filing of the company's research and development project materials.
6. Responsible for the review of drug quality standards and operating procedures.
7. Assisted the superior to complete the review and archiving of the batch records of entrusted products.
8. Responsible for the preparation of documents for FDA and customer audit or registration verification.
9. Responsible for the regular review of company documents to ensure that the documents used meet current requirements.
10. Responsible for the archiving of verification, confirmation, deviation, change, batch record, registration and other information.
11. Coordinated related personnel of various departments to complete the drafting and revision of quality system documents.
12. Responsible for making annual and quarterly training plans of the company and assisting the office in organizing company training.
13. Responsible for formulating annual and quarterly training plans for the quality management department, and organizing relevant training for the quality management department as planned.
14. Responsible for the recovery and filing of training records, and update personal training files quarterly.
15. Responsible for making annual quality review of commissioned products.
16. Assist superiors in quality system construction and continuous improvement.
17. Complete other tasks assigned by superiors.
Age requirement: 25-45 years old
1. Sorted out workshop quality management system, post SOP and other documents, organized staff within the department to prepare various business work plans, organized and held business meetings within the department, and checked the implementation of relevant work plans.
2. Responsible for the issuance and recovery of batch production records, batch inspection records and other controlled documents.
3. Organize workshop personnel for training.
Age requirement: 25-45 years old
1. Under the leadership of the Quality Management Department, assist the head of each department, workshop director and deputy director to do quality control and quality management in the process of drug production, with quality veto power.
2. Adhere to the quality inspection work, supervise and inspect the implementation of post SOP, prevent unqualified raw materials from being put into production, and unqualified semi-finished products from flowing into the next process. Responsible for the supervision and inspection of the clearance work.
3. Cooperate with workshop director to organize comprehensive quality analysis meeting regularly and educate staff to improve quality awareness.
4. Strictly control the process quality control points and monitor related technical indicators, and assist the workshop to take preventive measures to keep the process quality under control.
1. Major in microbiology, laboratory medicine, pharmacy, pharmaceutical analysis, food inspection, etc., more than half a year working experience in microbiology testing in pharmaceutical or food industry.
2. Responsible for the preservation and management of culture-medium and verified strains in microbiology laboratory.
3. Cooperate with the verification and testing of drug production workshop.
4. Responsible for microbial testing of raw and auxiliary materials, packaging materials and finished products of drugs.
Age requirement: 25-45 years old
1. Organized the formulation of quality management system, post SOP and other documents, organized staff within the department to prepare various business work plans, held business meetings within the department, and checked the implementation of relevant work plans.
2. Responsible for the quality audit of suppliers, and have the right to decide the qualification of raw materials, intermediates and finished products.
3. Responsible for reviewing and handling returned drugs and unqualified drugs.
4. Responsible for the quality supervision of the whole process of drug production.
5. Responsible for the examination and approval of various inspection reports.
6. Responsible for the review of batch production records, and write batch evaluation on the batch production records.
7. Responsible for organizing regular workshop quality upgrade plan and participating in drug quality analysis.
8. Responsible for reviewing plant, equipment, process, water production and other verification schemes, and supervise the implementation.
9. Other matters arranged by the leader.
10. QA Supervisor experience in pharmaceutical factory is preferred.
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