1. Responsible for optimizing the excipient manufacturing process and designing and developing study protocols under the guidance of the project leader;

2. Capable of independently carrying out and completing preparation-related experiments and providing assistance in completing lab-scale tests, pilot-scale tests and scale-up tests;

3. Assisting in excipient registration application: learning about the application requirements, and carrying out tests and data analyses and preparing application dossiers as required.

1. Bachelor degree or above in pharmacy, pharmaceuticals, chemistry and related majors;

2. Experienced in chemical preparation process research, especially in tablet preparation synthesis;

3. Familiar with regulations and guidelines for drug registration and the drug R&D quality research process;

4. Capable of reviewing literature, and reviewing and translating related foreign literature;

5. Have certain ability to make judgements and think independently.

1. Responsible for optimizing the excipient manufacturing process and designing and developing study protocols under the guidance of the project leader;

2. Capable of independently carrying out and completing preparation-related experiments and providing assistance in completing lab-scale tests, pilot-scale tests and scale-up tests;

3. Assisting in excipient registration application: learning about the application requirements, and carrying out tests and data analyses and preparing application dossiers as required.

1. Bachelor degree or above in pharmacy, pharmaceuticals, chemistry and related majors;

2. Experienced in chemical preparation process research, especially in research on tablet preparations;

3. Familiar with regulations and guidelines for drug registration and the drug R&D quality research process;

4. Capable of reviewing literature, and reviewing and translating related foreign literature;

5. Have certain ability to make judgements and think independently.