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高级质量体系工程师
1.6-2.6万
人 · 大专 · 5年及以上工作经验 · 性别不限2025/04/16发布
五险一金补充医疗保险免费班车餐饮补贴

工业园区通园路208号苏化科技园

公司信息
深圳尚科宁家科技有限公司

外资(欧美)/1000-5000人

该公司所有职位
职位描述
Our mission to positively impact people's lives every day in every home around the world allows our employees to be thinkers and tinkerers, designers and doers, creators and number crunchers, makers of things they love. As we continue to grow, we are excited to add Senior QMS Engineer to our global team.
OVERVIEW:
Assists QA manager for medical device quality system and regulatory management in manufacture process.
LOCATION: Suzhou
Here are some of the EXCITING things you’ll get to do:
Working Smart, Challenge and be challenge, Positive impact to the team, Clear and clean at operations and proactive.
Accountabilities:
Essential Functions
o Responsible for implementing and improving the medical device MFG quality system, ensuring its continued compliance with relevant requirements;
o Attend design transfer meetings and be responsible for implementing and improving the medical device production quality system, ensuring its compliance with relevant requirements;
o Manage and review batch records and related documents in the medical device production process;
o Report on the operation of the medical device MFG quality system and drive the resolution of MFG NCs;
o Evaluate the compliance and effectiveness of the quality system during the medical device MFG process, participate in internal audits and management reviews, promptly provide feedback and quality improvement suggestions;
o Assist in the promotion and training of medical device manufacture related regulations and product standards;
o Complete other tasks assigned by manager.
Hiring Requirements:
Experience:
61 Bachelor's degree or above in Mechanical, Electrical, Electronic, Pharmaceutical or related fields.
61 At least 5 years of experience in medical device production quality systems, familiar with ISO 13485 quality system and medical device regulatory requirements, with experience in quality management system writing or implementation preferred
61 Familiar with medical device system ISO13485, FDA, QSR820, independent promotion of the establishment and certification of medical system is preferred
Functional Skills/Knowledge
61 Fluent in oral and written English. The communication capability of Chinese will be perfect.
61 Quality system & regulation management background
61 Assesses, coaches, and monitors the developments of supplier.
61 Ability to work independently
61 Be honest, loyal to the work,
61 Strong code of ethics
61 Can be traveling when necessary

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