麦得科科技有限公司
质量体系工程师
2 years ago
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Important information
Contract type:
Permanent
Location:
Hangzhou, Zhejiang, China
Work mode:
Onsite
Published on:
7 August 2026
What they need
该职位来源于猎聘 岗位基本要求: 1、本科及以上学历;英语4级以上; 2、至少3年以上三类植入医疗器械相关工作经验;具有较强的质量体系知识和技能; 3、熟悉ISO13485质量管理体系和其他医疗器械质量标准的要求和实施方法; 4、熟悉医疗器械质量检验工作,有无菌、植入、眼科类医疗器械经验者优先; 5、良好的团队合作和协调能力; 6、拥有在生产环境下运行SPC、FMEA、PPAP等质量工具的经验、眼科类医疗器械优先;
岗位职责: 1、负责协调美国三类植入医疗器械公司体系运营,并及时处理和汇总异常;
2、负责主导质量体系相关记录审核工作;
3、负责统筹协调美国公司内外部审核等工作; 并帮助在必要时纠正问题; 4、负责配合美国公司工艺验证,参与编制方案、报告和数据的统计分析; 5、参与美国公司生产过程质量控制,数据统计分析等。
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