质量经理QA Manager
上海禹康医疗器械有限公司
- 公司规模:少于50人
- 公司行业:医疗设备/器械
职位信息
- 发布日期:2015-03-11
- 工作地点:上海-徐汇区
- 招聘人数:1
- 职位月薪:面议
- 职位类别:医疗器械生产/质量管理
职位描述
Responsibilities (fundamental job duties):
负责质量管理体系的建立、推行和维护,以符合FDA QSR, ISO13485及欧盟医疗器械指令的要求。
Be responsible for the establishment, execution and maintenance of the quality management system, which is in compliance with FDA QSR, ISO 13485 and MDD 93/42 EEC.
定期向管理层报告质量管理体系的运行情况。
Report to top management on regular basis the performance of the quality management system.
负责供应商质量管理和审核。
Be responsible for supplier quality audit and management .
负责产品放行批准的制定和执行。
Be responsible for defining product quality criteria and standard and final release.
负责组织不合格品评审。
Be responsible for nonconforming product review.
根据技术规范的要求,制订新产品的质量标准。
Base on the technical specification, set up quality standards and specifications for new products.
负责准备和协调与质量管理体系有关的审核或检查。
Be responsible for the coordination and preparation of external audits or inspections to quality management system.
负责纠正预防措施的实施和验证。
Be responsible for the implementation and verification of corrective and preventive actions.
负责与质量管理体系有关的数据分析。
Be responsible for quality management system related data analysis.
负责客户抱怨的处理。
Be responsible for customer complaint handling.
负责质量管理体系的策划。
Be responsible for quality management system planning.
负责产品设计开发的评审, 风险管理和更改控制。
Responsible for product design and development review, risk management and change control.
参与过程验证。
Participate in process validation.
参与质量管理体系内审和管理评审。
Participate in quality management system internal audit and management review.
岗位要求:
Minimum Requirements:
本科以上学历;
Bachelor degree or above;
5年以上质量管理体系运行经验,一次性医疗器械或塑料制品行业工作经验优先;
5+ years relevant experience in quality management system, with experience in single use medical device or plastic products industry is a plus;
国家注册质量工程师优先;
China Registered Quality Engineer is a plus;
具有ISO9001/ISO3485/ISO4001 内审员资格优先;
ISO9001/ISO13485/ISO14001 internal auditor is a plus;
较强的领导力;
Strong leadership;
良好的口头及书面沟通能力;
Good communication skills (both verbal and written);
中英文流利。
Be proficient in both English and/or Mandarin Chinese.
负责质量管理体系的建立、推行和维护,以符合FDA QSR, ISO13485及欧盟医疗器械指令的要求。
Be responsible for the establishment, execution and maintenance of the quality management system, which is in compliance with FDA QSR, ISO 13485 and MDD 93/42 EEC.
定期向管理层报告质量管理体系的运行情况。
Report to top management on regular basis the performance of the quality management system.
负责供应商质量管理和审核。
Be responsible for supplier quality audit and management .
负责产品放行批准的制定和执行。
Be responsible for defining product quality criteria and standard and final release.
负责组织不合格品评审。
Be responsible for nonconforming product review.
根据技术规范的要求,制订新产品的质量标准。
Base on the technical specification, set up quality standards and specifications for new products.
负责准备和协调与质量管理体系有关的审核或检查。
Be responsible for the coordination and preparation of external audits or inspections to quality management system.
负责纠正预防措施的实施和验证。
Be responsible for the implementation and verification of corrective and preventive actions.
负责与质量管理体系有关的数据分析。
Be responsible for quality management system related data analysis.
负责客户抱怨的处理。
Be responsible for customer complaint handling.
负责质量管理体系的策划。
Be responsible for quality management system planning.
负责产品设计开发的评审, 风险管理和更改控制。
Responsible for product design and development review, risk management and change control.
参与过程验证。
Participate in process validation.
参与质量管理体系内审和管理评审。
Participate in quality management system internal audit and management review.
岗位要求:
Minimum Requirements:
本科以上学历;
Bachelor degree or above;
5年以上质量管理体系运行经验,一次性医疗器械或塑料制品行业工作经验优先;
5+ years relevant experience in quality management system, with experience in single use medical device or plastic products industry is a plus;
国家注册质量工程师优先;
China Registered Quality Engineer is a plus;
具有ISO9001/ISO3485/ISO4001 内审员资格优先;
ISO9001/ISO13485/ISO14001 internal auditor is a plus;
较强的领导力;
Strong leadership;
良好的口头及书面沟通能力;
Good communication skills (both verbal and written);
中英文流利。
Be proficient in both English and/or Mandarin Chinese.
公司介绍
上海禹康医疗器械有限公司是一家专门从事医疗器械耗材出口的公司,位于上海市徐汇区。工厂设在江苏苏州。产品主要销往欧美等国,与国内外多家企业建立了良好的信誉合作关系。现因业务发展需要诚邀您的加入,我司将为您提供施展才华的平台、发展空间。
联系方式
- 公司地址:上班地址:徐汇区肇嘉浜路807号五洲国际大厦1106室(7.9号线肇嘉浜路站步行2分钟)