Process Engineer

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Non-Standard

Job Sub Function:
Non-Employee

Job Category:
Non-Standard

All Job Posting Locations:
Suzhou, Jiangsu, China

Job Description:



* Recommend, design, select machinery, tools, jigs, and fixtures required to machining the products.


*        建议、设计、选择加工产品所需的机械设备、刀具、工装与夹具。


* Work with other Manufacturing Engineers to maintain the item master, product routings and bills of material in the MRP system.


*        与其他制造工程师合作，在MRP系统中维护条款主文件、产品工艺路径和物料清单


* Deliver necessary training for workshop employees;


*        为车间员工提供必要的培训;


* Responsible for continuous improvement initiatives, such as projects to improve quality, cost, delivery and efficiency.


*        负责持续改进举措，例如改进质量、成本、交付和效率的项目


* Use PE principles to improve processes and reduce non-value-added waste and activities.

(Including process FMEA, Gauge R&R, Predictive Indicator and use of statistical techniques).


*        使用PE原则来改进流程并减少非附加值的浪费和活动。 （包括过程FMEA，Gauge R＆R，预   


*        测指标和统计技术的使用）。


* Participate to identify capital spend and budget requirements.


*        参与确定资本支出和预算需求。


* Participate or lead layout design / implementation for facility and equipment.


*        参与或领导设施和设备的布局设计/实施


* Support R&D on new products development and quality system implementation.


*        支持新产品开发和质量体系实施


* Understand the Quality philosophy based on FDA QSRs, ISO 9000 and SFDA requirements.


*        理解基于FDA QSR，ISO 9000和SFDA要求的质量理念


* Understand, compile and control non-conformance data and product tractability.


*        理解、编制和控制非符合项数据和产品易追溯性


* Responsible for creating and maintaining manufacturing documentation for equipment and processes.


*        负责创建和维护设备和流程的制造文件


* Responsible for compiling the validation/verification protocols and completing studies by creating finished reports.


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