职位描述
岗位职责:
1)运用NMR、HPLC, MS、NOE 等分析手段分析确定化合物结构
2)制定API质量标准,编写质量控制相关注册资料
以及API生产过程控制,原料,中间体,产品过程分析,规格设定
3)项目分析跟踪,稳定性研究方案编写
1) Use analytical techniques (e.g., NMR, HPLC, MS, NOE) for compound structure identification.
2) Establish API quality standards; prepare quality control-related registration documents.
3) Perform in-process control analysis of raw materials, intermediates, and products; set specifications.
4) Conduct project analytical tracking; draft stability study protocols.
任职要求:
多肽、小核酸、药物化学、有机化学、有机合成、药物合成、分析化学、生物化学等相关专业
Peptides, oligonucleotides, Medicinal Chemistry, Organic Chemistry, Organic Synthesis, Pharmaceutical Synthesis, Analytical Chemistry, Biochemistry, or related fields.