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Sr Quality Engineer-Medical Devices ID179665
1.5-2.5万
人 · 本科 · 5年及以上工作经验 · 性别不限2025/02/28发布
五险一金定期体检年终奖金

田林路600号

公司信息
捷普科技(上海)有限公司

外资(欧美)/1000-5000人

该公司所有职位
职位描述
Job Profile: Quality Group > Site Quality
SUMMARY
Represent the quality function of technical support, in conjunction with other internal support groups, regarding issues affecting manufacturing on global customer accounts. Serve as liaison between Jabil Circuit and suppliers or customers on global quality related issues.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
- Develop and maintain QA plans and timeliness of global new product introductions utilizing Advanced Product Quality Planning and Process Optimization specific to the customer.
- Evaluate and provide input to inspection processes via inspection aids and instruction guidelines.
- Develop appropriate systems for document storage, access and review pertaining to customer accounts.
- Review supplies, internal, and customer discrepancies, coordinate and track the effectiveness of corrective/proactive action efforts.
- Conduct periodic review and maintenance of all documentation files; Proactively conduct audit readiness review to ensure compliance.
- Participate in the vendor survey activities as applicable. Drive proactive participation with suppliers and (when possible) aid in their process improvement efforts.
- Interface with all departments as applied to the Policies and Procedures.
- Provide insight and assistance of implementing and maintaining Process Improvement and Optimization concentrating on proactive methodologies.
- Assist in driving the standardization of manufacturing processes. Taking lead of quality role in the New Product Introduction/ process realization stage. Ensure readiness and compliance to applicable standard and regulation.
- Interface and provide technical support on quality issues with the customer as needed.
- Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor.
- Comply and follow all procedures within the company security policy.
MINIMUM REQUIREMENTS
Bachelor's degree required and five years related experience; or equivalent combination of education and experience.
Experience in MAH/ NMPA product license or manufacturing license, familiar with medical device sterilization process will be of great advantage.

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