Post requirements
1. Bachelor degree or above, with a major in Pharmaceutical Analysis, Analytical Chemistry and other related fields, with more than 2 years of relevant working experience;
2. Familiar with various analytical instruments (HPCL, UV, dissolution meter, etc.) and conventional chemical analysis (titration, colorimetry, etc.);
3. Responsible, rigid, rigorous and meticulous, and have good team spirit;
Responsibility
1. Familiar with the latest technical requirements for drug review;
2. Check material, reference substance, reagent and chromatographic column in the process of R&D in time;
3. Responsible for the quality research of drug research and development, including the establishment of quality standards for APIs and their preparations, the development of analytical methods, the validation of analytical methods and the study of stability;
4. Responsible for the analysis and detection of samples in the process of drug research and development, including raw materials, intermediates, finished products and stability testing, and timely complete the original record of the experiment and experimental report and review in compliance with relevant requirements;
3. Responsible for reviewing relevant documents in drug R&D process, including SOP, methodological validation scheme and report, stability test scheme and report;
4. Responsible for technology transfer of analytical methods;
5. Write relevant declaration materials.