1. Responsible for the implementation of analytical experiments for the development of liposomes and new DDS for FDA and CFDA.
2. Receive, test, store and manage samples in accordance with analytical methods and related SOPs. Solve basic problems during experiments independently.
3. Write analysis and R&D plans and R&D reports in accordance with the standardized format and requirements, record original materials and draft relevant application materials for analysis and development.
4. Review the relevant research results completed by the project, including but not limited to product registration materials, original data, maps, etc.; Cooperate with the registration specialist to complete the technical and regulatory compliance confirmation work involved in product registration.

1. At least 2 or more years of relevant work experience in drug R&D quality research;
2. Familiar with the use and maintenance of various modern analytical instruments and conventional physical and chemical analysis instruments, proficient in the development andverification of analytical methods using various detection and analysis instruments, familiarwith relevant quality standards, and familiar with relevant regulations on drug declaration.