Clinical Manufacture

Commercial Manufacture

Drug Product Fill & Finish




Antibody Drug Conjugates

Technologies & Platforms


  • Lead a group of scientists to perform analytical method development/optimization, qualification/validation under cGMP.
  • Communicate with other functional areas and clients to ensure timely completion of QC activities to meet project timeline.
  • Review and approve technical documents such as methods, qualification/validation protocols and reports.
  • Serve as technical lead to solve technical challenges and support laboratory investigations.
  • Assist higher management to schedule resources, coordinate laboratory activities, and improve data and document quality to meet client expectation.


Basic Qualifications:

  • Graduate degree in analytical chemistry, biochemistry, molecular/cell biology or related fields. Relevant industrial working experience, 3-5 year for candidates with MS degree, 2-3 year for Ph.D. candidates.
  • Extensive knowledge and hands-on experience in the following areas:
  • Biochemical assays such as ELISA, cell based assay, qPCR, Western blot, enzyme activity testing
  • Separation assays such as HPLC, CE, gel electrophoresis
  • Biophysical assays such as MS, spectroscopy (UV, FTIR, CD, fluorescence, etc.), DSC.
  • Strong communication skills in English and Chinese, fluent in speaking, writing and reading in both languages.
  • Critical thinking, scientific reasoning and problem solving skills.
  • For Ph.D. candidates, proven track of record of scientific achievements.

Primary Location: China – Wuxi

To apply please send your application to