Quality Engineer
领萃企业管理顾问(深圳)有限公司
- 公司规模:少于50人
- 公司性质:外资(非欧美)
- 公司行业:贸易/进出口 医疗设备/器械
职位信息
- 发布日期:2017-05-22
- 工作地点:深圳
- 招聘人数:1人
- 工作经验:3-4年经验
- 学历要求:本科
- 语言要求:英语 粤语
- 职位月薪:0.8-1万/月
- 职位类别:医疗器械生产/质量管理 供应商管理
职位描述
职位描述:
Responsibilities:
1. Provides Technical support, compiling information from various sources to aid the identification and resolution of quality problems and initiatives.
2. Work directly with supplier’s Production Engineering and Quality Engineering Departments closely to plan and execute supplier’s product, semi-assembly and component in a systematic way to capture the quality improvement progress status.
3. To review and validate supplier test jig design and set up.
4. To review and improve supplier’s quality performance in a systematic way, with product / process related quality performance from IQC, IPQC, Production Fall Off rate, QA, OQA findings and customer feedbacks.
5. To capture the knowledge base for design practice, manufacturing process, test protocol, product quality evaluation framework for cross functionality between products and manufacturing sites.
6. DOA parts validation and root cause analysis push supplier to take CAP against material issues.
7. Provides Technical support, compiling information from various sources to aid the identification and resolution of quality problems and initiatives.
8. Review and approve non-conformances relating to disposition of non-conforming material while collaborating with customer team and Contract Manufacturer.
9. Review validation activities associated with various aspects of the product and testing equipment that is used in the manufacturing process.
10. Work with the Contract Manufacturer to ensure the health of their quality systems – focusing on Contract Manufacturer CAPA, SCAR, nonconformance closure and Supplier Performance.
11. Conduct weekly compliance/quality review with contract manufacturer team.
12. Coordinate requests from customer team to ensure timely information transfer to Contract Manufacturer.
Requirements:
1. Degree holder in engineering related, and at least 3 years of experience in the mechanical or industrial engineering, or an equivalent combination of education and experience.
2. Prior actual Medical Device Manufacturing, Quality Engineering, Reliability Engineering or Test Engineering experience with an industrial manufacturing firm experiences would be preferred.
3. Good English and Mandarin skills is a “must have”.
4. Robust understanding of CAPA and NC protocols, standard practices, and root cause analysis investigation techniques.
5. Ability to work independently and cross-functionally in a dynamic environment.
6. Work with suppliers based in Shenzhen and Huizhou areas
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Responsibilities:
1. Provides Technical support, compiling information from various sources to aid the identification and resolution of quality problems and initiatives.
2. Work directly with supplier’s Production Engineering and Quality Engineering Departments closely to plan and execute supplier’s product, semi-assembly and component in a systematic way to capture the quality improvement progress status.
3. To review and validate supplier test jig design and set up.
4. To review and improve supplier’s quality performance in a systematic way, with product / process related quality performance from IQC, IPQC, Production Fall Off rate, QA, OQA findings and customer feedbacks.
5. To capture the knowledge base for design practice, manufacturing process, test protocol, product quality evaluation framework for cross functionality between products and manufacturing sites.
6. DOA parts validation and root cause analysis push supplier to take CAP against material issues.
7. Provides Technical support, compiling information from various sources to aid the identification and resolution of quality problems and initiatives.
8. Review and approve non-conformances relating to disposition of non-conforming material while collaborating with customer team and Contract Manufacturer.
9. Review validation activities associated with various aspects of the product and testing equipment that is used in the manufacturing process.
10. Work with the Contract Manufacturer to ensure the health of their quality systems – focusing on Contract Manufacturer CAPA, SCAR, nonconformance closure and Supplier Performance.
11. Conduct weekly compliance/quality review with contract manufacturer team.
12. Coordinate requests from customer team to ensure timely information transfer to Contract Manufacturer.
Requirements:
1. Degree holder in engineering related, and at least 3 years of experience in the mechanical or industrial engineering, or an equivalent combination of education and experience.
2. Prior actual Medical Device Manufacturing, Quality Engineering, Reliability Engineering or Test Engineering experience with an industrial manufacturing firm experiences would be preferred.
3. Good English and Mandarin skills is a “must have”.
4. Robust understanding of CAPA and NC protocols, standard practices, and root cause analysis investigation techniques.
5. Ability to work independently and cross-functionally in a dynamic environment.
6. Work with suppliers based in Shenzhen and Huizhou areas
职能类别: 医疗器械生产/质量管理 供应商管理
关键字: Quality Engineer
公司介绍
We are Hong Kong based company with operation in Shenzhen, Lo Wu, China.
We are providing supply chain service to oversea customers, from product sourcing, quality evaluation, production monitoring till shipment.
We are providing supply chain service to oversea customers, from product sourcing, quality evaluation, production monitoring till shipment.
联系方式
- 公司地址:上班地址:惠州市