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QA Commissioner

Responsibilities:

1. Obey the leader of director, and be responsible for quality of products within charge area.

2. Observe each rules about corporate quality management, and carry out corporate quality policy and objects.  

3. Conduct daily work in compliance with GMP Requirements. Monitor production environments and facilities to adjust whether they are meeting specifications, if not, shall immediately provide feedback to relevant department or responsible person, and require reponsible person to carry out rectification before deadline.  

4. Be in charge of promptly stopping & disposing, as well as reporting to supervisor the behavior that does not conform to GMP Requirements happening in the management and production process of materials and products.    

5. Be responsible for monitoring the handling of unaccepted products, and timely fill in quality control record.  

6. Finish monthly analysis report of job as required, and promptly & forwardly report work to director.  

7. Be responsible for monitoring sampling intermediate product and finished product, and establish sample account according the operation of sample institution.    

8. Monitor & manage materials.

Qualifications:  College degree or above(or have Pharmacist qualification). Training experiences: Relevant knowledge training, GMP training, product manufacturing process training. Know of pharmaceutical regulations and GMP. Be familiar with production process and each parameter as well as each audit process of GMP. Have at least 3 years practical experience about pharmaceutical production or quality.

Business Address: North side of Jinjiang Road, Economic and Technological Development Zone, Suzhou, Anhui province

 QC Commissioner

Responsibilities:

1. Observe each rules about corporate quality testing, and carry out corporate quality policy and objects.  

2. Strictly implement GMP Specifications, and do daily work as GMP required.

3. Be responsible for testing incoming materials, intermediate product, and finished product and detect according to inspection operation specifications. Fill in relevant inspection record and issue inspection report.    

4. Be responsible for inspection and operation system of relevant product.

5. Count, analyze, dispose and report the testing data.

Qualifications:  College degree or above(or have Pharmacist qualification). Training experiences: Relevant knowledge training, GMP training, product manufacturing process training. Know of pharmaceutical regulations and GMP. Be familiar with production process and each parameter as well as each audit process of GMP. Have at least 3 years practical experience about pharmaceutical production or quality.

Business Address:  North side of Jinjiang Road, Economic and Technological Development Zone, Suzhou, Anhui province

Auditor of Engineering Settlement 

Responsible for:

1. making the terms of construction contract, and review price.
2. verifying the consistency of project contents, quantities, and realities evidenced by the compiling of budget and settlement of construction engineering project.

3. compliance regulations of applying quota of project budget and settlement. 

4. checking whether material price meet contract requirements, and settlement according to market price.
5. checking whether charging standard of budget and settlement fit in with contract provisions.
6. timely preparing record and reference of working diary.   
7. verifying construction progress and requirements of advance payments.
8. verifying authenticity, accuracy, and completeness of completion settlement documents.

9. strictly handling audit matters in accordance with procedure and quality standard of audit work. Pay attention to investigation and study. 

10. listening carefully to statements and explanations. Collect, arrange, and prepare working paper for achieved audit evidence. Try best to ensure audit quality, and reduce audit risks.
11. complying with professional ethics of audit, and strictly observe the rules of audit. Perform principles of audit by law, being loyal to duty, objective and fair, realistic, honest in performing official duties, and keeping secrets.
12. works of recording, arranging, generalizing, and analyzing for audit materials. Carefully write audit report and according to audit projects, do the work of classification and filing of audit materials.
13. under conditions of focusing on cost-effectiveness and without prior notice, carrying out check of advance control and intermediate control for the spot not less one time. Establish scheme before checking and give written report after checking.

14. assisting works temporarily assigned by other auditors, and perform other works assigned by audit director.
Requirements:
1. 23-50 years old. Male or Female. Sound in body and mind. Do not have infections disorder.
2. Be honest and upright, positive and optimistic , diligent and studious,and mild-mannered. Good at communication. Have a strong sense of service.

3. College degree. Major in engineering management and related subjects. Have experienced practical knowledge, and own the ability of working independently. Have abilities to communicate, coordinate and deal with emergencies.

4. 2+ years working experience about settlement management of engineering infrastructure. Having qualification certificate of cost member is preferred.

Business Address:  Jinxiu RD& Qinglongtan RD, Hefei High & Economy Development Zone, Hefei, Anhui Province

Tel: +0086-551-65386099