希玛德医疗器材（上海）有限公司
医疗器械注册
1 year ago
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Important information
Contract type:
Permanent
Location:
Shanghai, China
Work mode:
Onsite
Published on:
8 August 2026
What they need
该职位来源于猎聘 职责描述： 1、负责注册、法规文档的整理和归档 2、产品技术要求的起草 3、协助国外文件的翻译 4、注册文件的格式编辑 5、负责国家和行业标准更新的跟踪 任职要求： 1、熟悉医疗器械技术和标准，并对医疗器械法规有一定认识 2、医疗器械相关技术专业毕业 3、有吃苦耐劳的精神，并能保持不断学习和进取 4、查阅国内外专利、生物医学、临床数据等文献的能力 5、三年以上进口产品注册相关工作经验
6、英文六级或同等水平
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