Clinical Manufacture

Commercial Manufacture

Drug Product Fill & Finish




Antibody Drug Conjugates

Technologies & Platforms


  • Obey the company regulations;
  • Managing GMP documentation control
  • Managing Periodic document review;
  • Be responsible for managing GMP training and company annual training plan;
  • Be responsible for managing change control, deviation and CAPA;
  • Be responsible for construction, maintenance and management of Quality System Group;
  • Supporting Audit group to performing internal/external audit and follow up;
  • 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 6 years related working experience, familiar with the GMP/cGMP/EU GMP regulations;
  • Pass the all examinations before onto job(healthy situation , training);
  • Familiar with the usage of computer software;
  • With good English spoken and writing ability.

Primary Location: China – Shanghai

To apply please send your application to