RA Manager

无源三类产品 RAM
工作内容:
1.负责医疗器械的注册工作,与生产商进行沟通,完成文件撰写整理与申报,提前识别申报风险并跟进解决方案和进度。
2.与审评老师保持良好沟通,针对审评问题进行沟通协调,协同生产商积极提出解决方案,促进发补问题快速解决并按计划获得注册批准。
3.与生产商及各部门保持良好业务关系,及时沟通协作,协助法规识别分析,依照部门要求完成电子系统及线下表单填写,文档管理。
4.可以承担较高工作压力,互助协作为团队提供注册工作支持,完成领导交办的其它工作。
任职要求:
1.3年以上相关工作经验。
2.工作认真严谨 ,有较强的沟通、组织、表达力,具较强的工作责任心。

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1235869

Summary

Job Type
Permanent
Industry
Pharmaceuticals
Location
Beijing
Specialism
Life Sciences
Ref:
1235869

Talk to a consultant

Talk to Sarah Ma, the specialist consultant managing this position, located in Beijing
501, Tower 1, China Central Plaza, 81 Jianguo Road, Chaoyang District

Telephone: +861086487900

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