东莞 [切换城市] 东莞招聘东莞生物/制药/医疗器械招聘东莞医疗器械研发招聘

Senior Mechanical Engineer-MA

飞利浦(中国)投资有限公司 Philips (China) Investment Co.,Ltd.

  • 公司规模:10000人以上
  • 公司性质:外资(欧美)
  • 公司行业:多元化业务集团公司

职位信息

  • 发布日期:2020-10-05
  • 工作地点:深圳
  • 招聘人数:1人
  • 工作经验:8-9年经验
  • 学历要求:本科
  • 语言要求:英语熟练
  • 职位月薪:3-4万/月
  • 职位类别:医疗器械研发

职位描述

Senior Mechanical Engineer, MA Patient Monitors

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

·     Being responsible for the product definition and mechatronic solutions (including the mechanical and documentation aspects) in the development, realization and lifecycle management of medical devices and components.

·     Working with cross-function team to support device and component development via defining and realizing models and test set-ups.

·     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.

·     Leading or carrying out the detail design of key components, and supporting their realization.

·     Participating and leading as key competence resource in cross-functional and cross-business teams.

·     Being responsible for the manufacturability, interfacing and introduction of new technology and methods in manufacturing sites.

·     Working closely with the system engineers, architects, other functional representative and the project managers

·     Working closely with the commercial department to truly understand the customer’s technologic challenges in order to offer projects, tailored services & technical support.

·     Design process compliance assurance, design quality assurance and design reviews

·     Building an effective network with customers and suppliers, actively looking around to acquire new insights, to strengthen the knowledge base and competence of yourself in the domains of medical device and components.

·     Managing the product design documentation (the BOM and the Design History File).

·     Conducting the root-cause analysis of design, production problems and consumer complaints.


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's degree in Mechanical Engineering minimum (Master’s degree preferred).

·     8 years industrial experience (experience in medical device industry preferred).

·     Track record of product development life cycle from requirement, to design, to prototype, to verification and validation, to transfer to manufacturing, and to product release in medical device industry.

·     Strong knowledge and working experience in one or more relevant fields of competency, such as mechanical structure, plastic, heating & cooling, fluid mechanics, materials engineering, or in mechatronics and bio-mechanics.

·     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.

·     Design control process compliance management track record.


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, mechanical design tools – 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.

职能类别:医疗器械研发

公司介绍

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。

联系方式

  • Email:ruby.chen@philips.com
  • 公司地址:上海市静安区灵石路718号A1栋 (邮编:200233)
  • 电话:13774217703