

Job Description
1. Participate in the registration strategy planning and execution planning of RA CMC during the development of new drugs. Ensure the successful submission and advancement of drug registration processes for IND and NDA projects as planned.
2. Maintain timely and smooth communication with the drug development team and supply chain team.
3. Responsible for effectively promoting and completing drug registration review trials. Assist a professional team in solving experimental related issues.
4. Participate in daily communication with CDMO. Review all documents provided by CDMO.
5. Participate in the writing of pharmaceutical registration materials and the drafting and revision of SOPs related to RA CMC business within the company.
6. Compliance assurance related to CMC during drug development, such as compliance risk warning and development of improvement plans. Timely and effectively address potential compliance related issues.
Apply

Job Description
1. Participate in the registration strategy planning and execution planning of RA CMC during the development of new drugs. Ensure the successful submission and advancement of drug registration processes for IND and NDA projects as planned.
2. Maintain timely and smooth communication with the drug development team and supply chain team.
3. Responsible for effectively promoting and completing drug registration review trials. Assist a professional team in solving experimental related issues.
4. Participate in daily communication with CDMO. Review all documents provided by CDMO.
5. Participate in the writing of pharmaceutical registration materials and the drafting and revision of SOPs related to RA CMC business within the company.
6. Compliance assurance related to CMC during drug development, such as compliance risk warning and development of improvement plans. Timely and effectively address potential compliance related issues.
Apply
Phone:028-84919577
Email:hr@duoruipharm.com