【Sr. NPI Engineer 高级NPI工程师招聘】_秋时电子招聘信息-猎聘

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Recruitment Supervisor · 秋时电子

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职位介绍: 职位概要(Job summary): Working within a cross functional team in a collaborative and engaging manner, support the NPI programs by developing new processes and lead the transfer of the new product to mass production at the agreed quality levels. 工作职责(Responsibilities): 1. To enable new products to be successfully transferred to mass production, use lean techniques and tools to develop manufacturing processes including automated processes where applicable. 2. To ensure the final product specifications are suitable for mass production, influence product design by ensuring Design for Excellence guidelines is considered and followed. 3. Perform process verification and validation trials to determine and evaluate process repeatability & stability for new products. 4. Develop PFMEAs, Work instructions, Process flow layouts root-cause analysis investigations to ensure a high-quality throughput. 5. Manage NPI Engineers by facilitating regular 1-2-1 sessions to ensure engagement, motivation, timely resolution of issues as well as to address performance and training needs. 6. Provide visibility to NPI Team Leader of any H&S and technical issues that could inhibit mass production 7. Oversee and lead the requirements for any sample builds. 8. Drive manufacturing process efficiencies improvement opportunities ensuring robust feedback loops between departments. Communicate lessons learnt once products are in mass production. 9. Other duties and responsibilities assigned and delegated by the NPI Team Leader. 任职资格(Qualification): 1. A bachelor degree or above, at least 6 years relevant working experience of process developing experience in medical device company will be preferred. 2. Varied experience of launching new products into manufacture using a phase gated approach. 3. Good understanding in the use of lean and quality tools in a manufacturing environment. 4. Interpersonal, communication Problem solving, Analytical and lateral thinking skills. 5. Good quality mindset, FDA, ISO 13485 and medical device knowledge would be advantage. 6. Fluent English skills (written and spoken). 7. Professional, organized, passionate and self- motivated. 8. Willing to work overseas on business as needed.

其他信息: 语言要求：英语; 行业要求：全部行业; 所属部门：ENG

公司简介

公司简介 30多年来，Quasar 始终精耕细作，致力于为客户提供全面的全承包解决方案，从最初过程设计到大批量生产，为客户提供一系列不同的制造能力、专业支持以及项目优化服务。这种综合性工艺过程开发方法，是客户实现高品质的保证，同时还能节约成本。Quasar拥有全部国际相关证书，包括 ISO 13485:2016、cGMP 认证等，并严格遵守 IP 防护标准的规定。 Quasar的业务遍布全球，总部设在新加坡和中国香港，工程办公室设在以色列，在中国有三个制造工厂（分别位于深圳和东莞），在泰国有一个新建的制造工厂，在美国有一个业务发展部门。Quasar 拥有超过3000名员工，是微创医疗器械制造行业的市场领导者。我们的客户包括强生公司、美敦力以及雅培等大型跨国企业。

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