职位描述
工作职责:
1)能运用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.
任职资格:
专业要求: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.
综合要求:
1)具有良好的敬业精神和团队协作精神
2)专业基础扎实,能独立设计反应路线,熟练地查阅英文文献并进行总结提炼
3)良好的中文和英文书写和口语沟通能力,可与国外客户进行电话沟通,进行工作汇报
4)有意愿在中国发展
1) Strong sense of responsibility and teamwork spirit.
2) Solid foundational knowledge required. Ability to independently design synthetic routes, proficiently search and summarize English literature.
3) Strong written and verbal communication skills in both Chinese and English; capable of conducting teleconferences with international clients and delivering work reports.
4) Willingness to develop career in China."
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