Job Description: 1. Prepare the quality related procedure according to company requirement. 根据公司要求准备质量相关规程 2. Take charge of GMP document archiving.

负责GMP文件归档 3. Follow up the progress of documentation system building up追踪文件体系建立的进度 4. Review batch manufacturing records, packaging records, COAs and associated documentation in support of batch disposition. 审核批生产记录、包装记录、分析证明及相关文件，支持批处置。 5. Ensure that all the complaints are recorded, investigated and solved. 确保所有投诉得到记录、调查和解决。 Preferred Qualifications:

1. Bachelor degree or above in Pharmaceutical Engineering, Bio- Pharmaceutical Engineering, Analytical chemistry or Pharmacy Analysis related majors.

本科以上学历，机械、工程类 2. Basic English communication capability

基本的英语沟通技能 3. Strong team spirit

良好的团队精神 4. Excellent communication, problem-solving, planning and organization skills 良好的沟通、解决问题、计划和组织能力

5. Regular and reliable attendance, 3-4 business days per week

持续稳定可靠的出勤，一周3至4个工作日