Zhang Wei

Background

About Zhang Wei

A track-record proven leader with extensive experience in analytical chemistry, medicinal chemistry and chemical process development. Currently focus on qualitative & quantitative trance impurity analysis in drug product and chemical characterization of medical device & drug packaging/delivery systems. • Extensive experience in trace organic & inorganic analysis, such as Extractable & Leachable (E&L) and impurity analysis in drug product. • Extensive experience in quantitative chromatographic method development and validation per cGMP using GC-FID, GC-MS, HSGC-MS, LC-UV, UPLC-MS, and LC-MS/MS. • Expertise in E&L studies using GC-MS, HSGC-MS, UV-LC-MS and ICP-OES (trace metal analysis) per USP and ICH guidelines. • Excellent communication skills and technical presentation skills. • Excellent team-management and excellent interpersonal skills. • Broad knowledge and experience in analytical chemistry, organic chemistry, medicinal chemistry, organic synthesis, and chemical process development.