杭州招聘

1. Develop and maintain area/specific VPs
起草及维护区域/专题验证计划
2. Develop and maintain validation management procedures and SOPs
起草及维护验证管理程序及SOP
3. Writing and coordination of qualification/validation documentation according to VMPs or VPs
依据验证主计划和验证计划，起草及协调确认/验证文件
4. Evaluate and maintain validation related risks, such as process QRA, equipment RA, Cleaning RA, etc
评估和维护验证相关的风险，如工艺QRA、设备RA、清洁RA等
5. Execution of proper administration system of qualification/validation documents
执行良好的确认/验证文档管理
6. Be responsible for investigation, correction of deviations during validation execution.
负责验证执行中的偏差的调查及纠正。

浙江天元生物药业有限公司 诚聘