1. In accordance with the provisions of laws and regulations and the requirements of the drug regulatory authorities, summarize, compile and organize regulatory requirements and industry dynamics.

2. Interpret the regulations and policies related to the company's products, analyze the dynamics of policies and regulations in a timely manner, and put forward reasonable suggestions.

3. Analyze the potential impact on the company based on the dynamic changes of policies and regulations, and assist in formulating response strategies.

4. Provide registration regulations training to relevant personnel of the company and provide regulatory support.

5. Establish and improve relevant management systems of the department and assist in maintaining the relationship with the drug administration department.

6. Complete other tasks assigned by the leader.

1. Bachelor degree or above in medicine, pharmacy, biology, medical testing and other related majors.

2. 3 to 8 years of experience in collecting and interpreting regulations. Those with experience in collecting or interpreting regulations for drugs, cell therapy products, and cell drugs are preferred.

3. Familiar with the latest developments in drug regulatory laws and regulations, and proficient in office software.

4. Have strong information collection and analysis capabilities.

5. Have strong communication and language expression capabilities.