成都招聘

In this role, you have the opportunity to

Coordinate with PMO, PE and cross-functional team to execute Value Engineering and Quality/Availability/Cost improvements. In-scope products will include patient monitors, medical consumables and accessories, and potentially any products in MA.

You are responsible for

• Overall technical responsibility for realization of a new product or component release or sustaining activity – leading the analysis, design, test, troubleshoot, document of internal or supplier mechatronic systems and/or sub-systems.

• Translation of user requirements, regulatory requirements, manufacturing requirements, service requirements, process requirements into device and component requirement specification, interface speciation, and top level device and component design.

• Requirements management, decomposition of derived requirements, feasibility of potential solutions, design options and decision, verification and validation planning and design.

• Leading or develop new and optimize existing product concepts within cross-functional teams, or leading and controlling outsourcing of these activities, and aligned with R&D development project roadmap.

• Build prototypes for feasibility, functionality, and performance assessments.

• Develop design output, from schematics, BOM, to dFMEA, DFT, DFM, risk management, verification & validation plans and reports, etc.

• Collaborate with cross-functional teams regarding standards compliance and global regulatory requirements (e.g. IEC 60601-1, IEC 60601-1-2, ISO 14971, FDA cGMP, QSR, ISO 13485, EU MDR).

• Design process compliance assurance, design quality assurance. Lead design reviews and EC process.

• Technical management of medical device and components during product life cycle.

• Design risk management

• Defect management

You are a part of

A professional R&D team with around 70 team peers in Shenzhen China.

To succeed in this role, you should have the following skills and experience

Qualifications:

• Bachelor of Science in Systems, Electrical, Computer Science, Physics, Biomedical Engineering or equivalent degree in a Scientific/Engineering discipline.

• 8+ years of experience in an engineering role beyond the educational qualification.

• Evidence of practical knowledge of standards and regulations pertaining to the medical device industry, both domestic and international. This includes but is not limited to organizations such as FDA, IEC, ISO, CFDA, ACR, AAPM, COCIR, MITA and other directives such as RoHS and WEEE. Examples include: FDA 21CFR820.30, IEC 60601-1 and ISO 14971.

• Proven excellence in technical leadership in a matrix environment, including demonstrated ability to influence indirect resources.

• Design control process management track record

• Working knowledge of tools and processes related to system configuration management from specifications development, traceability, version control, defect tracking and field feedback.

• Knowledge and experience spanning multiple engineering disciplines (e.g. mechanical, software and systems engineering).

  Skills:

• Demonstrable clear oral communication, as well as well-organized documentation skills; excellent command of written and spoken English.

• Ability to drive solutions and decisions in a cross-functional team environment.

• Experience in requirements management tool, design quality management tools, risk management tools, and problem reporting/defect tracking tools.

• Hands on experience on FMEA, Fault Tree analysis, Reliability block diagrams preparation and RCA techniques, design and simulation tools and CADs.

• Demonstrated capability to conduct and lead technical reviews of product design elements.

• Demonstrated ability in leading evolution of a complex feature, where analysis requires both evaluation of multiple candidate solutions and significant evaluation of intangibles.

In return, we offer you

A promising professional career development platform. Work in the medical industry brings much fulfillment, as well as unique challenges; you will be empowered to drive groundbreaking innovations with a globally recognized, premium brand behind you.

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。

创美好，做真我，迎蜕变。
我们深信每一个你都卓尔不凡, 更期待与志同道合的你笃行致远。