Responsibilities:
1.Responsible for LIMS, LES and other system management, including system configuration, maintenance and training.
2.Responsible for LIMS static configuration.
3.Responsible for recipe building for the analytic method in QC.
4.Responsible for related system SOP, change controls, deviations and abnormal event.
5.Responsible for system data management.

Requirement:
1.Bachelor or master degree with major in Biology, Chemistry or Pharmaceutical analysis field.
2. At lease 2 years of GMP experience.
3.Familiar with LIMS, Empower, LES and other E-Systems in QC is preferred.
4.Good computer operation skill (intermediate level in Microsoft Word, Excel, PowerPoint, Power BI, Minitab etc.
5.Fluent in writing and reading in both Chinese and English.
6.Critical thinking, scientific reasoning and problem solving skills