质量体系专员
职位描述
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职位职责 (简要说明)
1.Ensures that the local Quality Management System meets current regulatory requirements and comply with local business operation;
2. Lead Development and/or Improvement of Quality system;
3. Improve and optimize the corrective action and preventive action system.
主要工作内容/职责(列举清单)
1.Ensures that the local Quality Management System meets current regulatory requirements and comply with local business operation;
2. Ensures Cooperate policies are implemented within local SOPs within the local QMS as appropriate
3. Assist with development and/or Improvement of Quality System procedures and processes;
4. Assist with internal and supplier audit development, implementation, and execution;
5.Provide support to internal functions in the application, maintenance and improvement of medical quality systems and department specific processes;
6. Improve and optimize the corrective action and preventive action system for medical projects to ensure the compliance of FDA QSR820, ISO 13485:2003, etc.;
7.Responsible for managing 3rd party audit, regulatory compliance agency inspection;
8. Document control management for medical project;
9. Other tasks assigned.
任职资格
知识/教育程度
1. Bachelor’s Degree in Engineering, Science, or health-related field
2. Familiar with Quality system Improvement tools, such as 8D, fish bone, 5why,etc.
经验/能力要求
1. 3-5 years related work experience in Quality Management system, at least two years’ experience as quality system engineer or above.
2. Quality Systems development, implementation, and training experience
3. Experience with ISO 9001, TS 16949 system requirements and training, ISO 13485 is preferred.
4. Must be able to work independently and have ability to work with cross-functional teams
5. Extensive project management skills with the ability to work under tight timelines and able to multi-task
6.Must have an understanding of fundamental quality system processes for design, CAPA and manufacturing in a regulated industry.
7. Familiar with MS-OFFICE;
8.Good communication and team work;
9. Fluency in oral and written English.
企业简介
常州市康辉医疗器械有限公司于1997年08月25日在常州国家高新区(新北区)市场监督管理局登记成立。法定代表人张晓川,公司经营范围包括三类6846植入材料及人工器官,二类6815注射穿刺器械等。
[展开全文] [收缩全文]职位发布企业
康辉医疗器械
企业性质:民营企业
企业规模:50-99人
成立年份:1997
企业网址:http://cn.kanghui-med.com/cn/index.html
企业地址:常州市新北区长江北路11号
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职位发布日期: 2019-04-16