杭州招聘

1. 负责批签发摘要填写、批签发资料整理及抽样。
Responsible for filling in lot release summary、data compilation And sampling

2. 负责填写、上报生物制品批签发管理系统，联络跟踪批签发进度及相关信息，确保批签发工作及时有效进行。
Responsible for fill in report lot release management system.
3. 制作批签发合格证及产品质量报告，并发放、登记。
Make lot release certificate 、Product quality report ，And issued, registration.
4. 根据新质量体系要求进行相关审核评估改进，并修订审核相关SOP。
According to New quality system requirements related assessment improvement ， review and revised Related SOP and Master batch record.
5、负责批签发前、产品上市放行前批记录审核。Responsible for Batch release before、Product to zhe market before Batch record audit。
6.负责杭州市远程监管系统填报、核对工作。
Responsible for Hangzhou FDA remote monitoring system fill, check the work。
7.协助完成部门工作以及上级下达的各项临时任务.
Assist department to work ，Complete the temporary task issued at a higher level

浙江天元生物药业有限公司 诚聘