Calibration Engineer 校验工程师
强生(苏州)医疗器材有限公司
- 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:2016-10-10
- 工作地点:苏州
- 招聘人数:1人
- 工作经验:5-7年经验
- 学历要求:本科
- 语言要求:英语 熟练
- 职位月薪:1500以下/月
- 职位类别:其他
职位描述
职位描述:
Descriptions:
? Perform the principal duties of the Calibration function
o Management of calibration team, and make sure all activities by the team conducted following Johnson & Johnson requirements and regulation requirements.
o Guarantee that all measurements systems existing in the Suzhou site in China are calibrated, inspected, checked and maintained in a timely and compliant manner.
o Develop, verify and modify all inspection programs (including CMM, shadowgraph etc..).
o In connection with other departments in China and Overseas, to guarantee in time and compliant manufacturing start-up in China in order to support all business objectives.
o In partnership with manufacturing department.
? Understand and maintain all the inspection, measuring and test equipments related to a given group of products.
? Create and maintain the required procedures, instructions and inspection methods to assure the expected quality of the products in accordance with all applicable requirements.
? Compile and control non-conformance data.
? Propose, develop and implement programs to improve quality, scrap rates, lead times, or any other program defined by the management.
o Support R&D on new products development.
? In accordance with DePuy Worldwide Quality strategy, participate to the development of the quality system and its day to day implementation:
o Participate in training or workshop employees and deploy on site the Quality philosophy based on FDA QSRs, ISO 9000 and SFDA requirements.
o Ensures compliance to all GMPs and MDD requirements.
o Conduct internal and supplier quality audits as required.
? Perform all job duties in full accordance with:
o The J&J policies on Information, Assets protection, Maintain password(s) confidential, protect critical Business Information.
o All J&J policies and local regulations.
o The policies of the Health Care and Environmental programs.
o The code of conducts policies.
? Full responsibility and ownership (like all employees on site) for all audits (internal, Corporate, External, for Quality, H&S, Environment, etc…)
? Oversee FAI inspection to meet cross functional requirements such as product transfer, R&D and NPI
? Conduct Measure system Analysis such as GR&R if applicable.
Qualifications:
? Strong technical skills
? Strong work ethic
? Influencing Skills
? Negotiating Skills
? Effective Communicator
? Planning & Organizing Skills
? Judgment
? Fair & Reasonable Approach
? Confidentiality
? Customer and Quality focus
? Strong ability to work in a cross functional structure
? Degree in Mechanical/Production Engineering or 3 years experience and demonstrated skills
? Statistics and Process capability
? Project Management
? English at a business level
举报
分享
Descriptions:
? Perform the principal duties of the Calibration function
o Management of calibration team, and make sure all activities by the team conducted following Johnson & Johnson requirements and regulation requirements.
o Guarantee that all measurements systems existing in the Suzhou site in China are calibrated, inspected, checked and maintained in a timely and compliant manner.
o Develop, verify and modify all inspection programs (including CMM, shadowgraph etc..).
o In connection with other departments in China and Overseas, to guarantee in time and compliant manufacturing start-up in China in order to support all business objectives.
o In partnership with manufacturing department.
? Understand and maintain all the inspection, measuring and test equipments related to a given group of products.
? Create and maintain the required procedures, instructions and inspection methods to assure the expected quality of the products in accordance with all applicable requirements.
? Compile and control non-conformance data.
? Propose, develop and implement programs to improve quality, scrap rates, lead times, or any other program defined by the management.
o Support R&D on new products development.
? In accordance with DePuy Worldwide Quality strategy, participate to the development of the quality system and its day to day implementation:
o Participate in training or workshop employees and deploy on site the Quality philosophy based on FDA QSRs, ISO 9000 and SFDA requirements.
o Ensures compliance to all GMPs and MDD requirements.
o Conduct internal and supplier quality audits as required.
? Perform all job duties in full accordance with:
o The J&J policies on Information, Assets protection, Maintain password(s) confidential, protect critical Business Information.
o All J&J policies and local regulations.
o The policies of the Health Care and Environmental programs.
o The code of conducts policies.
? Full responsibility and ownership (like all employees on site) for all audits (internal, Corporate, External, for Quality, H&S, Environment, etc…)
? Oversee FAI inspection to meet cross functional requirements such as product transfer, R&D and NPI
? Conduct Measure system Analysis such as GR&R if applicable.
Qualifications:
? Strong technical skills
? Strong work ethic
? Influencing Skills
? Negotiating Skills
? Effective Communicator
? Planning & Organizing Skills
? Judgment
? Fair & Reasonable Approach
? Confidentiality
? Customer and Quality focus
? Strong ability to work in a cross functional structure
? Degree in Mechanical/Production Engineering or 3 years experience and demonstrated skills
? Statistics and Process capability
? Project Management
? English at a business level
职能类别: 其他
公司介绍
强生(苏州)医疗器材有限公司诚聘
联系方式
- Email:jjmszl@its.jnj.com
- 公司地址:地址:span上海