Inspection Supervisor
史赛克(苏州)医疗技术有限公司
- 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
职位信息
- 发布日期:2013-01-21
- 工作地点:苏州
- 招聘人数:若干
- 工作经验:五年以上
- 学历要求:本科
- 语言要求:英语精通
- 职位类别:质量管理/测试主管(QA/QC主管)
职位描述
任职要求:•5+ years in the Quality function or equivalent experience
•Good knowledge in MSA, inspection, and G R&R.
•Good experience in project management is preferred.
•Knowledge in machining is a Plus.
•B.S. in engineering, engineering
Understand and be able to apply, enforce, comply and meet all GMP standards and quality requirements.
•Familiar with analytical tools, such as FMEA, process control plan and SPC.
•Excellent interpersonal communication and supervisory skills.
•Good PC skills
职位职责:•Continuously fully comply with all GMP and Regulatory requirements.
•Implement Stryker Corporate Quality policies and standards. Ensure compliance to GMP and ISO 13485 requirements.
•Responsible to stop further processing in the event of encountering non-conforming products condition.
•Manage, engage and develop the inspection team.
•Ensure inspection equipment and gages are properly used, maintained and calibrated on shop floor.
•Defines, specifies, and/or approves the implementation of standards, methods, and procedures for inspection, testing, and evaluating the precision, accuracy and reliability of company products.
•Manage the inspection teams
•Train and/or coordinate the training and required qualifications of personnel within assigned area.
•Provide Quality supervision on production floor, WH, facility to ensure the most current/validated method/process and specification are implemented and DHR for every lot is correctly filled in per GMP & QS requirements.
•Work with related team on inspection method optimization and inspection efficiency improvement.
•Work with related teams on our Quality KPIs to make sure we meet or exceed our target.
•Partner with our operations team to ensure a smooth flow of product through the inspection process.
•Develop, coordinate and/or implement root cause problem solving, preventive and corrective actions.
•May be involved in product transfer.
•May be involved in internal/external Quality audits and communicate results.
•Be the system owner for QS based on authorization.
•Release RM/Component/Product at first level based on authorization.
•Other tasks assigned by supervisor.
•Good knowledge in MSA, inspection, and G R&R.
•Good experience in project management is preferred.
•Knowledge in machining is a Plus.
•B.S. in engineering, engineering
Understand and be able to apply, enforce, comply and meet all GMP standards and quality requirements.
•Familiar with analytical tools, such as FMEA, process control plan and SPC.
•Excellent interpersonal communication and supervisory skills.
•Good PC skills
职位职责:•Continuously fully comply with all GMP and Regulatory requirements.
•Implement Stryker Corporate Quality policies and standards. Ensure compliance to GMP and ISO 13485 requirements.
•Responsible to stop further processing in the event of encountering non-conforming products condition.
•Manage, engage and develop the inspection team.
•Ensure inspection equipment and gages are properly used, maintained and calibrated on shop floor.
•Defines, specifies, and/or approves the implementation of standards, methods, and procedures for inspection, testing, and evaluating the precision, accuracy and reliability of company products.
•Manage the inspection teams
•Train and/or coordinate the training and required qualifications of personnel within assigned area.
•Provide Quality supervision on production floor, WH, facility to ensure the most current/validated method/process and specification are implemented and DHR for every lot is correctly filled in per GMP & QS requirements.
•Work with related team on inspection method optimization and inspection efficiency improvement.
•Work with related teams on our Quality KPIs to make sure we meet or exceed our target.
•Partner with our operations team to ensure a smooth flow of product through the inspection process.
•Develop, coordinate and/or implement root cause problem solving, preventive and corrective actions.
•May be involved in product transfer.
•May be involved in internal/external Quality audits and communicate results.
•Be the system owner for QS based on authorization.
•Release RM/Component/Product at first level based on authorization.
•Other tasks assigned by supervisor.
公司介绍
我们,来自美国!
我们,创建于1941年,并已发展为全球规模最大、技术最为领先的医疗技术公司之一!
在全球拥有29个生产和研发基地;
在全球100多个国家和地区销售产品;
拥有近22000余名优秀的员工!
2013年全球业务超90亿美金,并连续32余年保持业务增长——平均每年增长19%!
在骨科植入物、手术介入治疗设备、医疗通讯、数字化影像系统等医疗领域引领技术创新
2012在《财富》500强中排名第308位,并在由《财富》评选的“最受敬仰的医疗设备及其它精密设备行业”
中排名第6!
我们,多次荣获盖洛普公司评定的“***工作场所奖”
我们,曾于2005-2008年连续4年获得医疗产品和医疗器械行业“最受尊敬企业”荣誉;
我们,曾于2007-2009年连续3年被授予盖洛普“***雇主奖”
我们,被《中国医疗设备》评选为“2010年优秀售后服务商第2名”
我们,于2011年被《福布斯》杂志授予全球“最具创新力”公司;
我们,于2010-2013连续4年被《财富》杂志授予美国“***工作场所奖”;
……
这,就是史赛克医疗技术有限公司!
史赛克(苏州)医疗技术有限公司成立于2007年11月,位于苏州工业园区出口加工区a区,为史赛克集团在亚洲投资的第一个制造工厂,公司将快速成长为集团最大的综合性生产基地之一、并肩负起为集团全球业务供应众多优质治疗产品的使命!
在史赛克苏州,
我们有一个激情洋溢、追求卓越的团队;
我们为员工提供极具竞争力的薪资报酬;
我们致力于创造优质的医疗产品,以帮助人们更为健康、快乐的享受生活!
如果您正在寻找一份与众不同的工作经历,来吧,加入史赛克!
在史赛克,你的天赋将不断地被发现、强化和运用!
更多公司信息请浏览公司网站:www.stryker.com
我们,创建于1941年,并已发展为全球规模最大、技术最为领先的医疗技术公司之一!
在全球拥有29个生产和研发基地;
在全球100多个国家和地区销售产品;
拥有近22000余名优秀的员工!
2013年全球业务超90亿美金,并连续32余年保持业务增长——平均每年增长19%!
在骨科植入物、手术介入治疗设备、医疗通讯、数字化影像系统等医疗领域引领技术创新
2012在《财富》500强中排名第308位,并在由《财富》评选的“最受敬仰的医疗设备及其它精密设备行业”
中排名第6!
我们,多次荣获盖洛普公司评定的“***工作场所奖”
我们,曾于2005-2008年连续4年获得医疗产品和医疗器械行业“最受尊敬企业”荣誉;
我们,曾于2007-2009年连续3年被授予盖洛普“***雇主奖”
我们,被《中国医疗设备》评选为“2010年优秀售后服务商第2名”
我们,于2011年被《福布斯》杂志授予全球“最具创新力”公司;
我们,于2010-2013连续4年被《财富》杂志授予美国“***工作场所奖”;
……
这,就是史赛克医疗技术有限公司!
史赛克(苏州)医疗技术有限公司成立于2007年11月,位于苏州工业园区出口加工区a区,为史赛克集团在亚洲投资的第一个制造工厂,公司将快速成长为集团最大的综合性生产基地之一、并肩负起为集团全球业务供应众多优质治疗产品的使命!
在史赛克苏州,
我们有一个激情洋溢、追求卓越的团队;
我们为员工提供极具竞争力的薪资报酬;
我们致力于创造优质的医疗产品,以帮助人们更为健康、快乐的享受生活!
如果您正在寻找一份与众不同的工作经历,来吧,加入史赛克!
在史赛克,你的天赋将不断地被发现、强化和运用!
更多公司信息请浏览公司网站:www.stryker.com
联系方式
- 公司地址:上班地址:江苏省苏州市工业园区苏虹中路200号出口加工区A区吴巷18号