1.Participate in the research and development of the company's product line, responsible for the development of experiments, including the screening of tumor therapy-related targets. The researcher will be responsible for the research and development of the company's product line, including the screening of tumor therapeutic targets, the identification of stable cell lines, and the characterization and identification of exosomes to obtain exosomal drugs with anti-tumor efficacy.

2.Coordinate the different aspects of R&D, data entry. Management and statistical analysis.

3.According to the company's development needs, through preliminary research and hotspot tracking, combined with experimental research, to provide a scientific basis and test basis for the company's new drug development and project, and write relevant research reports.

4.Responsible for frontier tracking, literature research, and continuous development of new drug candidates.

5.Responsible for coordinating and tracking work with the company to ensure the smooth progress of the project.

1.Mainly engaged in process development exploration and research, design of experimental protocols, the establishment of experimental methods, and subsequent technical optimization.

2.Responsible for donor cell reactor culture conditions and process parameters exploration and optimization.

3.Responsible for completing the purification process development. Amplification. Transferring and optimizing the technology for small-scale trials.

4.Responsible for stability analysis. Optimization of storage conditions and other experimental exploration.

5.Responsible for formulation prescription screening and determination of final dosage form.

6.Responsible for frontier tracking, literature research and reporting.

7.Assist in the completion of exogenous gene therapy related topics.

8.Assist in the daily maintenance of equipment and facilities to ensure the normal operation of the platform instruments and equipment. Do the daily maintenance and management of laboratory equipment.

9.Coordinate and resolve problems that may arise during the experimental process in a timely manner. Solve problems that may arise in the experimental process, grasp the progress of the project test, and regular project progress reports, to ensure that the project is completed within the specified time.

1.Mainly responsible for the implementation of bioanalytical assays for our products, such as ELISA, qPCR, virus titer assay, genomic DNA extraction, etc.

2.Responsible for the implementation of bioanalytical methodological validation experiments. Optimization.

3.Responsible for the investigation and analysis of laboratory deviations/changes/OOS records related to the testing process and timely reporting of abnormalities.

4.Responsible for daily testing and key reagents used in the production process. Molecular biology-related experiments in material release inspection.

5.Responsible for writing GMP documents such as SOPs for molecular biology-related analytical methods, management SOPs, method verification or validation protocols and reports.

6.Perform daily laboratory activities in accordance with QC laboratory regulations and relevant regulatory requirements.

7.Required to assist in other QC testing-related work.

1.Responsible for the testing and report writing of our pre-clinical biological samples.

2.Responsible for the routine testing of toxic species products.

3.Responsible for the routine testing of CMC products for small trials.

4.Responsible for the daily management of testing reagents, consumables and instruments.

5.Participate in the formal validation of bioanalytical assays.

6.Participate in the development and continuous optimization of bioanalytical assays.

7.Participate in the validation program and validation report writing, review and implementation.

8.Participate in the management and reassessment of all internal standards and key reagents in the department.

9.Participate in the writing of SOPs, reports, ROA, etc., and archiving of experimental reports and other documents in the department.

10.Complete other work as assigned by the supervisor.