QUALITY MANAGER
东莞利康医疗器械有限公司
- 公司规模:150-500人
- 公司性质:外资(欧美)
- 公司行业:医疗设备/器械 电子技术/半导体/集成电路
职位信息
- 发布日期:2014-04-16
- 工作地点:东莞
- 招聘人数:1
- 工作经验:八年以上
- 学历要求:本科
- 语言要求:英语熟练
- 职位类别:品质经理
职位描述
Reports to: Quality Director, Hong Kong
Job Description:
Quality Manger is responsible for ISO14385 and FDA Quality Systems Regulations program for the China factory. This position will have overall responsibility for assuring that Quality system requirements are effectively established, implemented and maintained in compliance with CGMP’s and other regulatory requirements. In this role you will –
RESPONSIBILITIES
? Responsible for assuring that AgaMatrix China sites comply with all related aspects of regulatory agency compliance.
? Obtain and maintain certification to ISO 13485, China SFDA and FDA site registration.
? Direct quality personnel in the China factory, training, implementation and monitoring of quality procedures.
? Develop Quality System procedures to enhance overall Quality performance and compliance.
? Assure that all sites are trained and understand all current regulatory requirements.
? Host all medical device related site audits. Document audit results and communicate to management responsible for the sites audited all finding, observations and any resulting Corrective Actions.
? Conduct internal quality audits at regular intervals to assure that the Quality System is in compliance with the established Quality System requirements to determine the effectiveness of the Quality System and report to executive management on their effectiveness.
? Review all external audit requirements, results pre and post.
? Will participate in the coordination, review, investigation and documenting of complaints relating to possible medical device reporting as required by the applicable, FDA, ISO and EN quality system requirements.
? Drive the correction, prevention and documenting customer complaints investigations which may be relating to possible medical device reporting as required.
? Assure that all China sites are trained and understand all current Quality System requirements.
QUALIFICATIONS
? BS or BA in a biomedical science, engineering or medical technology.
? 8+ years experience in quality assurance for medical devices.
? Proven leadership skills.
? Supervisory and management experience. Strong communication skills.
? Proficiency in written and spoken English, Cantonese and Mandarin
? Ability to travel, if needed
Job Description:
Quality Manger is responsible for ISO14385 and FDA Quality Systems Regulations program for the China factory. This position will have overall responsibility for assuring that Quality system requirements are effectively established, implemented and maintained in compliance with CGMP’s and other regulatory requirements. In this role you will –
RESPONSIBILITIES
? Responsible for assuring that AgaMatrix China sites comply with all related aspects of regulatory agency compliance.
? Obtain and maintain certification to ISO 13485, China SFDA and FDA site registration.
? Direct quality personnel in the China factory, training, implementation and monitoring of quality procedures.
? Develop Quality System procedures to enhance overall Quality performance and compliance.
? Assure that all sites are trained and understand all current regulatory requirements.
? Host all medical device related site audits. Document audit results and communicate to management responsible for the sites audited all finding, observations and any resulting Corrective Actions.
? Conduct internal quality audits at regular intervals to assure that the Quality System is in compliance with the established Quality System requirements to determine the effectiveness of the Quality System and report to executive management on their effectiveness.
? Review all external audit requirements, results pre and post.
? Will participate in the coordination, review, investigation and documenting of complaints relating to possible medical device reporting as required by the applicable, FDA, ISO and EN quality system requirements.
? Drive the correction, prevention and documenting customer complaints investigations which may be relating to possible medical device reporting as required.
? Assure that all China sites are trained and understand all current Quality System requirements.
QUALIFICATIONS
? BS or BA in a biomedical science, engineering or medical technology.
? 8+ years experience in quality assurance for medical devices.
? Proven leadership skills.
? Supervisory and management experience. Strong communication skills.
? Proficiency in written and spoken English, Cantonese and Mandarin
? Ability to travel, if needed
公司介绍
厂房面积超过8千平方公尺, 并拥有行业全套先进生产设备, 主要生产设备均由美国进口。
公司福利:
1、公司免费提供早餐、午餐、晚餐(午、晚餐为三菜一汤)。
2、公司为夜班员工提供相应的夜班补贴。
3、公司免费提供住宿,水电费全免。
4、职员每周五天8小时制。
5、工资发放准时,全员社保。
公司福利:
1、公司免费提供早餐、午餐、晚餐(午、晚餐为三菜一汤)。
2、公司为夜班员工提供相应的夜班补贴。
3、公司免费提供住宿,水电费全免。
4、职员每周五天8小时制。
5、工资发放准时,全员社保。
联系方式
- 公司地址:上班地址:广东省东莞市樟木头镇银洋工业区