苏州招聘

Responsible:
?The primary objective of this position is to work on the product transfer projects at suppliers to

achieve excellent quality, delivery and cost goals.
?Identify and ensure proper transfer training needs for new technologies.
?Continuously fully comply will all GMP standard requirements.
?Responsible to stop further processing in the event of encountering non-conforming products condition.
?Transfer production lines from product transfer project to production within selected suppliers.

Participate in project teams as key outside process representative.
?Production in process control plan design and execution at supplier site if required.
?Process problems, NCR investigation, corrective action plan and execution during project transfer at

supplier.
?Transfer the knowledge from the project team to responsible SQE team after transfer.
?Drive for continuous improvement in quality, delivery and cost.
?Continuously fully comply with all GMP standard /ISO 13485 requirements.
?Maintain the local Quality system and implement all quality requirements.
?Provide guidance on Quality Assurance/GMP/FDA-QSR related topics.
?Develop, coordinate and/or implement root cause problem solving, preventive and corrective actions.

Analyzes reports and/or returned products and recommends corrective action at supplier.
?Work as key project leader for product transfer and management of supplier related PPAP process.
?Set supplier performance program and objectives and makes sure that targets are achieved by monitoring

performance/trending against defined parameters.
?Communicate status of the projects; establish and execute systematic project review and update process
?Conduct external audits and may support internal audits.
?Support Product verification, Process validation, Reliability testing and Component qualification at

supplier.
?Responsible for Supplier process controls.
?Drive supplier performance improvements.
?Identify priorities, helping Stryker to allocate the right resources for project execution.
?Ensure that the validated manufacturing processes are adhered to and any changes are communicated in

advance and in accordance with our company established standards
?Other tasks assigned by Supervisor.
?CNC machining knowledge, or other manufacturing knowledge.
?Good command of MS Office software.
?Problem investigation and corrective action implementation capability.
?Familiar with the project management tools.
?Knowledge on lean and GMP.
?ISO 13485 or similar quality system knowledge.
?CNC programming capability is preferred.
?Data analysis skill.
?Energetic, selfinitiative and independent individual Demonstrated Collaboration, Negotiation & Conflict

Resolution

Skills
?Fluent in English and Chinese in both technical and business speaking and writing skills.
?Excellent communication and presentation skills in both English and Chinese.
?Preferred knowledge of various Manufacturing Processes (machining, powder coating, metal stamping,

forming, plastics and rubber molding, machining, secondary processes etc).
?Solid understanding of problem-solving processes and tools – 6-sigma training and certification and proven ability to apply them a plus
?Must be able to observe and note minute inconsistencies.
?Must be able to generate, follow, and explain detailed instructions and inspection procedures of the

responsible areas accurately.
?Familiar with analytical tools, such as FMEA, process control plan and SPC.
?Familiar with Blueprint/engineering schematic reading and interpretation
?Basic inspection techniques

Requirement
?More than 3 years in Quality Assurance, Manufacturing or related functional area
?5years relevant experience of supplier development /quality, project management, sourcing in a precision engineering manufacturing environment - medical device industry a plus or equivalent high tech industry.
?Experience on working in an environment with multiple projects and varied release cycles. Must have

excellent planning, prioritization and organizational skills.
?Experienced in GMP or ISO quality systems
?Experienced in machining inspection, method selection, gauge calibration is preferred.

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