Chemical synthesis

1. Responsible for reviewing and determining the raw material development plan for the R&D project.

3. Continuously follow up on and understand the process and regulations related to generic drug development and product application, and participate in the writing and modification of application materials.

4. Familiar and master the laboratory safety regulations, correctly operate various instruments and equipment.

5. Actively cooperate with the department and other departments in communication and cooperation, and complete project application-related work.

6. Collaborate with project management related data statistics and other related work, complete other tasks assigned by the leader.

1. Be responsible for the review and determination of the raw material development plan for the R&D project.
2. Be responsible for the synthesis required for API (Active Pharmaceutical Ingredient) registration, process optimization and purification, as well as pilot-scale-up production. And be responsible for the specific implementation of the chemical API of the R&D project at the base.
3. Continuously follow up on the processes and regulations related to generic drug R&D and product registration, and participate in the preparation and modification of registration documents.
4. Be familiar with and master the laboratory safety regulations, and correctly operate various instruments and equipment.
5. Actively cooperate with the communication and cooperation between the department and other departments, and complete the work related to project registration.
6. Cooperate with the relevant data statistics of project management and other related work, and complete other tasks assigned by the leader.
7. Relevant experience in generic drug projects (which can also be project management) is required, and the ability to comprehensively arrange generic drug API projects is needed.

BASE: Guangzhou Huangpu District