Responsibilities

1. Responsible for the research and organizational management of genetic engineering drugs (peptides, proteins) projects.

2. Responsible for genetic construction of genetic engineering drugs, seed cultivation and screening, process design.

3. Troubleshooting during experimental processes, pilot and production technology transfer.

4. Reviewing and writing application materials.

5. Responsible for project communication, coordination to ensure smooth progress of project research.

Qualifications

1. Master's degree or above in biology, medicine, chemistry, or related fields, with 2 years or more work experience.

2. Ability to lead project teams in conducting research on genetic engineering drug processes, with expertise in genetic construction of genetic engineering drugs, seed cultivation and screening, fermentation, and purification technologies. Knowledge in drug purification and impurity research, experience in pilot and production technology transfer, and a proven track record in genetic engineering drug research are preferred.

3. Proficiency in searching domestic and international drug research literature, patent databases, and regulatory evaluation documents related to drugs.

4. Familiarity with drug development research processes, understanding of current domestic and international regulatory requirements and guidelines for genetic engineering drug research and registration, and experience in drug application documentation work are advantageous.