深圳招聘

职位描述：
Key Areas of Responsibility：

1. Participate to review product CRS, SRS, SDS/PDS, RMF, Safety & Regulation requirement, etc. Estimate requirement testability and sufficiency.
2. Participate in electric structure design, responsible for cable design, label design and warning mark design, etc. Assemble and debug prototypes to verify Service Requirement and Manufacturing Engineer Requirement.
3. Trace and review ME/Service Validation activities, Reliability test and EMC/Safety test, join in reliability and EMC improvement.
4. Support product regulation certification and register.
5. Develop Verification Plan (include but not limited to: )
- Review product requirement specification and clearly understand each requirement in requirement specification documentation
- Estimate resource (manpower and capital) requirement for certain amount of verification work
- Understand the analysis of hazardous impact of medical product to different personnel (patient, operator, etc...)
- Develop test case per each requirement in requirement specification documentation
- Schedule test case review meeting with relevant parties
6. Perform verification testing ,track product problem (include but not limited to: )
- Setup test environment per Verification Plan
- Execute each test case on test bays
- Log defect to defect management tool
- Update test cases’ execution result to test case management tool
- Attend defect review meeting and join team to analyze defect impacts to test deliverables
     - Trace requirement matrix and output traceability map.
     - Optimize verification technology and process, communication and sharing with other guys and departments.
7. Develop Verification Report (include but not limited to: )
- Draft verification report in the end of each beta cycle
- Schedule verification report review meeting with relevant parties
- Get verification report approved in Agile system
8. Provide procedure and technical training to new engineers (include but not limited to: )
- Understand all procedures which are deployed in R& D department
- Understand all technical knowledge which are required for medical products’ verification
- Present above knowledge to new engineers when they are onboard .
9. Develop unit and system auto testplatform HW and SW.

Job Requirements & Skills

1. Bachelor’s Degree in Engineering ;
2. At least 8 years’ experience in product’s verification position ;
3. Medical products’ experience is much preferred ;
4. Strong interpersonal and communication skills with the ability to communicate with different functions, e.g. System, Physics, SW, etc... ;
5. Knowledge of the V-model development cycle ;
6. Knowledge of hardware, embedded software and auto-test software;
7. Familiar SPI and RS485/232 communication protocol, NI Labview experience is much preferred;
8. Good knowledge of the English language (both written and verbal). 举报 分享

荷兰皇家飞利浦公司是一家领先的健康科技公司，致力于在从健康生活方式、疾病预防、到诊断、治疗和家庭护理的整个“健康关护全程”，凭借先进的技术、丰富的临床经验和深刻的消费者洞察，不断推出整合的创新解决方案，助力健康医疗系统实现四重目标——提高大众健康水平、提高医护人员满意度、改善患者体验，并降低关护成本。飞利浦的愿景是通过有意义的创新，令世界更健康、更可持续的发展，到2030年每年改善25亿人的生活。

        飞利浦公司总部位于荷兰，2021年销售额达172亿欧元，在全球拥有大约78,000名员工，销售和服务遍布世界100多个国家。公司目前在诊断影像、图像引导治疗、病人监护、医疗信息化以及消费者健康和家庭护理领域处于领导地位。

        在飞利浦，每一个人，都至关重要。这是我们始终坚持的信念。在飞利浦，你将用数字化驱动有意义的创新，积极影响自己与数十亿人的生活，践行改善人类生活的使命。我们全心营造多元包容的工作环境，平等互助的工作氛围，让你的独特之处得到充分尊重和欣赏，鼓励你释放真我，以梦为马，不负韶华。本着 “立足中国，辐射全球” 的理念，我们通过布局广泛的业务线，为你带来广阔的平台、丰富的学习资源、多样的内部发展机会，助你成为具备全球化视野和本土深度的一专多能复合型稀缺人才。

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