Assistant Operation Manager Fco jobs at Philips in China

10+ years working experience in manufacture industry, development field or comprehensive working background. Better in medical device industry. Familiar with product development procedure. English can be taken as working language....

Drive all elements of the Physics and System Engineering function (composed of Image chain Physics, Algorithm and System) to achieve best in class proficiency. Develop and execute a strategic plan...

Establishing system verification team, and to cultivate qualified employees for support product development and maintenance, to realize the goal of department. Helping team member continue improve the knowledge and skill,...

Lead, facilitate, improve CAPA process and drive CAPA activities from issue identification to closure. Maintain and manage an effective CAPA system to meet the requirements of appropriate global. regulations and...

独立处理内部及客户反馈的品质问题，有效降低客户拒收比率；跟进新项目转产过程的品质需求， 确保所有的新项目顺利转产且符合法规和品质要求； 确保新项目顺利转产和转产后产品质量的持续改善，确保生产模具和设备完成验证。. 协调新产品转生产前所有的品质要求已达成；. 协调产品在注册前后的各种品质需求的达成及品质系统的完善；. 协调实施产品风险管理和风险分析，建立产品风险管理文档，确保产品质量符合客户要求的同时，产品的任何风险得到有效预防和控制，以确保产品安全、有效和高度的可靠性；. 协调过程更改并确保整个更改过程的文件和样板正确更改；. 完成相关的过程确认和特殊工序和设备的验证，确保生产正常及顺利转产；确保生产过程符合法规要求；. 完成新项目的量测方法和量测的重复性和再现性确认；. 推进过程改善行动，确保成品内部拒收率达成目标;. 执行市场反馈分析，确保主要产品的退货率持续降低；. 提供技术支持和方法，协助生产线有效控制品质并持续降低品质控制成本；. 独立处理内部及客户反馈的品质问题，有效及时处理客户投诉，并确保措施的有效性。. 学历: 本科或以上学历，理工科优先. 工作经验: 0-4年品质工作经验. 能力和技能: 熟悉ISO13485标准& FDA 21 CFR 820 QSR 法规,了解行业内不同区域品质体系相关的法规要求，有一定品质体系建立维护经验；. 熟悉并掌握QC7大手法，并能使用不同的品质控制工具。. 能阅读和书写英文；....

Implement and maintain the regular activities on existing HK & GBA approvals, and accelerate compliance to HK& GBA requirements, and meet performance target. Coordinate, review, and file new device registration/approvals...

To establish a professional system verification team, cultivate qualified employees to support product development and maintenance by conducting productive and meaningful system level verification, to ensure high quality of design...