GLP QA Leader

岗位描述

  • 参与制订、修订、审核SOP,并审核SOP的分发、回收、销毁等文档工作;
  • 负责与GLP实验室QAU部门相关的所有文件管理工作;
  • 检查研究项目实验过程操作中的关键环节;
  • 审核试验方案、试验记录和总结报告;
  • 定期检查动物饲养设施、实验仪器设备、档案管理和供试品管理工作;
  • 向SD、部门负责人和机构负责人书面报告检查发现的问题,并跟踪整改情况;
  • 负责实施供应商审计,接待客户的审计工作;
  • 对检查/审计结果进行阶段性分析,并对机构工作人员进行GLP规范性培训;
  • 其他与GLP实验室质量体系相关的工作。

任职要求

  • 本科以上学位,医药、生物、药理学、毒理学等专业
  • 具有至少三年GLP毒理实验室QA工作经验(动物实验相关)
  • 口语和书面表达能力较强
  • 英文书写能力较强

地点:中国,江苏启东,滨海高新技术园区

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Headquarters

1F & 3F, Block A
2829 JinKe Road
Zhangjiang Hi-Tech Park
PuDong New Area
Shanghai China, 201203

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Contact Us

China: +86 21 5132 0088
US: +1 650 419 9974
Europe: +45 4586 9000
Japan: +81 03 5403 6975

contact@chempartner.com