Clinical Manufacture

Commercial Manufacture

Drug Product Fill & Finish




Antibody Drug Conjugates

Technologies & Platforms


  • Obey the company regulations;
  • Be responsible for the reviewing of batch testing record;
  • Be responsible for ensuring the integrality and accuracy of related report list;
  • Be responsible for reviewing the integrality and accuracy of validation protocol/report;
  • Be responsible for reviewing abnormal situation which related with product quality activities;
  • participate in internal and external audit, collect self-inspection results and track the result verification of corrective actions;
  • Be responsible for the drafting and revising of relevant documents;
  • Report to supervisor of the job periodically;
  • Finish the other jobs assigned by supervisor.


Basic Qualifications:

  • With the education background of medicine or relevant major of bachelor or above, with more than 2 years related working experience, familiar with the GMP/cGMP/EU GMP regulations and CFDA regulations;
  • Pass the all examinations before onto job(healthy situation , training);
  • Familiar with the usage of statistical software;
  • With good English reading and writing ability.

Primary Location: China – Shanghai

To apply please send your application to