Clinical Manufacture

Commercial Manufacture

Drug Product Fill & Finish




Antibody Drug Conjugates

Technologies & Platforms


  • Responsible for optimizing change control、CAPA、Deviation procedure;
  • Responsible for informing training of change control、CAPA、Deviation procedure;
  • Responsible for assigning change control/CAPA/deviation number and fill in related records;
  • Responsible for tracking the implementation of change control/CAPA/deviation plan;
  • Responsible for summarizing quarterly review for deviation;
  • Responsible for the archive of change control/CAPA/deviation related records;


Basic Qualifications:

  • Bachelor degree or above, major in biology, pharmacy, chemistry, or other related major;
  • 2 years’ experiences of QA in pharmaceutical industry is preferred;
  • Well verse in spoken and written English language,skillful in using computer software;
  • Excellent communication, problem-solving, and organization skills, attentive, careful and meticulous, with strong team-work ability.


Primary Location: China – Shanghai

To apply please send your application to