Quality质量Manager-欧美独资公司,制造型工厂,专业医疗设备知名品牌,广阔发展
上海帝博企业管理咨询有限公司
- 公司规模:少于50人
- 公司性质:外资(欧美)
- 公司行业:专业服务(咨询、人力资源、财会)
职位信息
- 发布日期:2013-07-18
- 工作地点:苏州
- 招聘人数:1
- 职位类别:质量管理/测试经理(QA/QC经理)
职位描述
Quality Manager
欧美独资公司,制造型工厂,专业医疗设备知名品牌,广阔发展,丰厚薪资
上班地点:苏州工业园区
职位概述以及职责范围:
? Implement, monitor and enforce all quality functions (QM, QA, QC) according to local, international and Company standards.
? Fulfill all qualification and validation task to comply with China and B. Braun guidelines
? Qualified Person responsibility
? Maintain cost leadership for all responsible areas
? Stretching and implement the Company quality system within China for CoE VS & CHIP operations
主要职责及绩效标准:
· Set up and continuously improve the QM system
· Set up and adjust the Validation Master Plan (VMP) with all related Qualification and Validation tasks
· Ensure GMP compliance and customer/group quality standard
· Product/production/GMP license application and award
· Plan, define and install QA and QC areas in CoE VS & CHIP project
· Train subordinates and company staff on Quality Issues whenever needed
· Fulfill all duties in most cost effective manner
· Responsible for product release/rejection as per company quality standard
· Act as management representative on quality related issues of CoE VS & CHIP China division
· Other ad-hoc assignments by superior(s)
教育背景要求:
· Bachelor degree in engineering or medical technology. Master Degree preferred
经验及知识要求:
· Minimum 5 years working experience in managerial position with a multinational medical device company
· Solid experience in medical device quality management which includes quality assurance, quality control and validation.
· Familiar with local and European medical device (SFDA MDs ISO 13485/ cGMP )
特殊技能及能力要求:
· Leader and team worker
· Excellent communication and interpersonal skills
· Good planning and prioritizing skill
· Strong business sense
其他要求:
· Full Mandarin & English speaking and
· writing abilities
工作环境
· Office and all plant areas
欧美独资公司,制造型工厂,专业医疗设备知名品牌,广阔发展,丰厚薪资
上班地点:苏州工业园区
职位概述以及职责范围:
? Implement, monitor and enforce all quality functions (QM, QA, QC) according to local, international and Company standards.
? Fulfill all qualification and validation task to comply with China and B. Braun guidelines
? Qualified Person responsibility
? Maintain cost leadership for all responsible areas
? Stretching and implement the Company quality system within China for CoE VS & CHIP operations
主要职责及绩效标准:
· Set up and continuously improve the QM system
· Set up and adjust the Validation Master Plan (VMP) with all related Qualification and Validation tasks
· Ensure GMP compliance and customer/group quality standard
· Product/production/GMP license application and award
· Plan, define and install QA and QC areas in CoE VS & CHIP project
· Train subordinates and company staff on Quality Issues whenever needed
· Fulfill all duties in most cost effective manner
· Responsible for product release/rejection as per company quality standard
· Act as management representative on quality related issues of CoE VS & CHIP China division
· Other ad-hoc assignments by superior(s)
教育背景要求:
· Bachelor degree in engineering or medical technology. Master Degree preferred
经验及知识要求:
· Minimum 5 years working experience in managerial position with a multinational medical device company
· Solid experience in medical device quality management which includes quality assurance, quality control and validation.
· Familiar with local and European medical device (SFDA MDs ISO 13485/ cGMP )
特殊技能及能力要求:
· Leader and team worker
· Excellent communication and interpersonal skills
· Good planning and prioritizing skill
· Strong business sense
其他要求:
· Full Mandarin & English speaking and
· writing abilities
工作环境
· Office and all plant areas
公司介绍
DB Talent is a European based recruitment company. Our Shanghai office opened in the 2001, and we have continually provided excellent professional service to our clients and candidates.
联系方式
- 联系人:resume
- 电话:13701722965