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Sr. Manufacturing Engineer 12-18K
秋时电子科技(东莞)有限公司 ENG 广东东莞 2天前刷新
学历要求大专 工作经验5年 现居住地不限

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职位介绍

职位概要(Job summary):
Quasar’s Manufacturing Engineering Team has the responsibility of working with cross-functional teams comprising of Quality, Production, Supply Chain and Program Departments to achieve organization’s goals. Manufacturing Engineers own the processes for one or more product lines and are responsible for implementing Continuous Improvement Projects (CIPs), working together with RFQ Engineer to provide accurate Technical Costing and building samples for new projects. Manufacturing Engineers works closely with Advanced Engineering Team and New Product Introduction (NPI) Team to execute a clean handover of projects from NPI to Mass Production.
工作职责(Responsibilities):
1. Health & Safety: Ensure that all Health, Safety and Environmental requirements are fulfilled for the manufacturing process.
2. Quality: Drive Engineering solutions to ensure Right First-Time principles, driving yield improvements, complaint reductions, supporting the CAPA process, and audit prep activities.
3. Continuous Improvement: Own the manufacturing process, work with key business stakeholders and operations teams to assess process capabilities, improve process efficiency, reduce cycle time.
4. Service: Drives a culture of Exceptional Customer Experience (ECE) for both the Internal and External customers, by ensuring that projects and commitments and continually being met or exceeded.
5. New opportunity sample build: Conduct the new opportunity sample build, by ensuring that product and commitments being met or showing manufacture capability to customer.
6. Responsible for managing the overall process performance through the appropriate use of Lean Manufacturing tools and techniques (TPM etc.).
7. Responsible for preparing validation protocol of OQ&PQ/PV for additional TJ/equipment, and process period to mass production.
8. Develop and manage SOPs/manufacturing standards/operations standard work as required in compliance with engineering change control process (ECO).
9. Investigating in state-of-the-art process technologies and evaluating potential competitive advantage and the cost-benefit of introduction.
10. Maintain high quality / compliance standards in line with Medical Devices manufacturing requirements.
11. Drive MP product to keep stably high manufacturing yield.
12. Manage a variable workload to meet operational requirements.
任职资格(Qualification) :
1. College degree or above, major in engineering, mechanical, electronic, or equivalent.
2. Above 5-years’ + related working experience. Medical product development/manufacturing will be preferred.
3. Strong in failure analysis, root cause analysis, and corrective action implementation.
4. Demonstrate a dynamic, motivated & flexible approach to work with results-oriented attitude.
5. Demonstrate a practical understanding of Lean Manufacturing principles and statistics.
6. Excellent communication, planning and organizational skills.
7. Fluent English skills.
8. Skillful AutoCAD and MS office (SolidWorks/Pro-E skills is an advantage)
5936 6444-|171 6451 8006 029. Knowledge of ISO & FDA compliance is an advantage.

公司信息
行业:
医疗设备、医疗器械
规模:
1000人以上
地址:
广东东莞广东省东莞市松山湖莞台生物技术合作育成中心8号楼