taiheng-凯发平台

job description

1. independently carried out formulation research, including formulation design, process research, stability study, process amplification and technology transfer, etc.;
2. responsible for recording and sorting the technical and original data of the project to ensure the authenticity and traceability of the experimental data;
3. responsible for writing the information of the prescription and process in the drug submission, and assist in registration and submission;
4. responsible for searching the chinese and english literature, following up the latest research progress in the domestic and overseas, and conducting research;
5. responsible for the use and maintenance of relevant test instruments.

application conditions

1. master degree or above in pharmaceutical formulation or pharmacy, chemical engineering, polymer materials, etc.;
2. familiar with the properties and preparation process of solid oral formulations, and know how to use equipment (analytical skills are preferred);
3. familiar with china's drug development policies and regulations and relevant technical requirements; understand gmp related regulations; have experience in anda development and familiar with ich regulations is preferred;
4. proficient in reading english professional literature and writing project plans and experimental reports;
5. strong learning, working, anti-pressure ability and cooperative spirit; be able to communicate well with colleagues;
6. welcome overseas returnees and foreign talents (foreign nationals are not required to speak chinese).