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- 职位介绍
- Your tasks and responsibilities: You will be responsible for system level product definition, design, implementation and performance evaluation. Co-work with the internal and external partners to deliver the best quality product according to the customer needs. And you will be responsible for the product registration technical support, Product configuration and lifecycle management and maintenance. 1. Responsible for the product high level requirements definition and flow down 2. Responsible for the preparation and Review of the Product Design History File and other Program Files. 3. Responsible for the Communication with the OEM supplier for the design implementation and Lead Design Review. 4. Responsibility for the Design Output Management (Drawing, Code, BOM, etc.). 5. Responsibility for product NMPA Registration Dossier Preparation and Review, support V&V Test and Type Testing. 6. Responsibility for product quality evaluation. 7. Responsibility for product design change. 8. Technical support for Custom Compliant Handing after product release. Your qualifications and experience: 1. You have Bachelor’s degree or above, major in Biomedical Engineering, Electrical Engineering, Physics, Mechatronics, Computer Science, or closely related discipline. 2. You have over 5 years’ experience in Ultrasound medical device system engineering work. 3. You have solid experience of medical product NMPA registration and quality compliance audit. 4. You have rich experience in Product lifecycle maintenance and sustaining. 5. You have general ability to cooperate with internal and external partners.
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