士卓曼(北京)医疗器械贸易有限公司
法规注册实习生
2 months ago
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Important information
Contract type:
Permanent
Location:
Shanghai, China
Work mode:
Onsite
Published on:
16 August 2026
What they need
该职位来源于猎聘 主要工作职能: 1. 协助整理、收集产品注册相关文件; 2. 撰写注册所需的相关技术文档; 3. 协助核对注册资料,确保文件完整、准确; 4. 支持团队日常项目执行及跨部门沟通协调; 5. 协助翻译质量体系文件,并完成部门交办的其他工作。 任职要求: 1. 本科及以上学历,研究生学历优先; 2. 专业不限,生物医学工程等相关专业优先; 3. 熟练使用Word、Excel、PowerPoint等办公软件; 4. 英语听说读写能力良好; 5. 每周能够实习3天及以上,实习期不少于3个月。
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