北京德迈特科技发展有限公司
国际注册专员(J10003)
3 months ago
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Important information
Contract type:
Permanent
Location:
Beijing, China
Work mode:
Onsite
Published on:
7 August 2026
What they need
该职位来源于猎聘 1、负责海外医疗器械注册文件的编制、审核和提交； 2、研究并了解国外医疗器械注册相关法律法规、政策，不断更新和完善公司的注册策略和流程； 3、协调各部门完成相关文件的准备工作，确保文件的及时提交和审批； 4、解决注册过程中出现的问题和难题，保证公司产品正常注册上市和合规管理； 5、上级领导安排的其他相关工作。 任职资格 1、统招本科及以上学历，理工科背景，医学等相关专业，英语6级； 2、有一定的医疗器械生产企业的工作背景； 3、工作细心，责任心强； 4、对13485质量体系有一定了解；
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