Job description

Job responsibilities:

1. Responsible for the quality research of new or generic drugs, formulating quality standards, and investigating stability, etc.;

2. Assist to complete the retrieval of Chinese and English documents, and track the latest research progress at home and abroad;

3. Write the application materials for the analysis part;

4. Hand over analysis methods and quality standards with customers;

5. Assist to complete other work related to drug analysis and quality research.

Job requirements:

1. Major in pharmaceutical analysis or pharmacy, bachelor degree or above, with more than 5 years of relevant work experience;

2. Ability to independently complete the quality research and stability research of chemical drugs;

3. Excellent experimental operation ability, proficient in using conventional analytical instruments such as high-performance liquid phase and gas phase, and proficient in daily maintenance of analytical instruments;

4. Familiar with the technical requirements of new drug registration regulations and guidelines;

5. Familiar with the writing and sorting of application materials, and be able to independently write registered application materials and original records;

6. Familiar with common medical websites and databases, and have a strong ability to retrieve literature;

7. Honesty, integrity, strong sense of responsibility, good team spirit and cooperative spirit.