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Senior Manufacturing & Quality Engineer – Medical Devices & Consumer Electronics

MatchaTalent

远程工作

地点
Remote (Malaysia)
工作安排
Full Time
发布日期
2026年10月10日

申请前,请在雇主网站确认职位仍在招聘,并检查完整要求和条件。

职位描述

此界面为简体中文。雇主发布的职位名称和描述保留原文,可能为英文。

This role is open to candidates based in Johor Bahru, Kuala Lumpur, or Penang, Malaysia. The position is remote with regional travel as required. Client Overview Our client is a publicly traded healthcare technology company specializing in digital musculoskeletal (MSK) healthcare solutions. The company combines advanced wearable sensors, computer vision technology, and clinical care to deliver accessible and technology-driven healthcare solutions at scale. With a strong presence across the healthcare technology ecosystem, the organization works with enterprise clients, health plans, healthcare providers, and strategic partners to improve patient outcomes while reducing healthcare costs. Its technology portfolio includes connected hardware and digital health solutions that require robust manufacturing, quality, and supply chain processes. As the company continues to scale its hardware and medical device operations, it is seeking an experienced Manufacturing & Quality Engineer to strengthen manufacturing processes, supplier quality, product validation, and production readiness across its hardware ecosystem. Job Role The Senior Manufacturing & Quality Engineer – Medical Devices & Consumer Electronics will play a key role in ensuring that hardware products, manufacturing processes, fixtures, tooling, and quality systems are designed, validated, and maintained for efficient and reliable mass production. The role will work closely with contract manufacturers, component suppliers, engineering teams, and internal product and operations stakeholders throughout the product lifecycle—from new product introduction (NPI) through mass production. The ideal candidate brings strong hands-on experience in manufacturing engineering, quality engineering, mechanical/electrical engineering, or related disciplines, with a proven track record supporting high-volume consumer electronics and/or medical device manufacturing. Key Responsibilities Lead the development, validation, implementation, and maintenance of manufacturing processes, fixtures, tooling, and production systems for high-volume manufacturing. Develop and optimize fabrication, assembly, testing, and packaging processes to achieve high quality, reliability, efficiency, and cost effectiveness. Ensure component suppliers and contract manufacturers consistently meet product design, fabrication, assembly, testing, and quality requirements. Lead day-to-day execution of hardware quality processes across manufacturing and supplier operations. Support and drive New Product Introduction (NPI) programs from early development through EVT, DVT, PVT, and mass production. Lead yield improvement, cost reduction, process validation, root-cause analysis, and manufacturing efficiency initiatives. Apply pFMEA, Process Validation, CAPA, and structured problem-solving methodologies to identify and resolve manufacturing and quality issues. Collaborate with contract manufacturers under CM, JDM, ODM, and OEM models and ensure clear alignment of responsibilities and quality expectations. Work closely with component suppliers and EMS partners to resolve technical, quality, and production issues. Support the development of a world-class hardware operations and product organization with strong end-to-end manufacturing and supply chain capabilities. Engage with contract manufacturers and suppliers remotely and onsite as required. Communicate complex technical issues clearly to both technical and non-technical stakeholders. Drive consensus and effective collaboration across engineering, product, operations, quality, and supplier teams. Travel within the region as required to support suppliers, manufacturing sites, and project activities. Candidate Requirements Bachelor's or Master's Degree in Manufacturing Engineering, Mechanical Engineering, Electrical Engineering, Quality Engineering, or a related engineering discipline. Minimum 9+ years of professional experience, preferably with 10+ years in manufacturing process support, manufacturing engineering, or quality engineering roles. Proven experience taking hardware products from product development through NPI and mass production in high-volume manufacturing environments. Strong experience in consumer electronics and/or electro-mechanical medical device manufacturing. Hands-on knowledge of manufacturing and qualification processes including injection molding, metal fabrication, electronic components, SMT, batteries, FATP, and packaging. Extensive experience working with EMS contract manufacturers under CM, JDM, ODM, and/or OEM models. Strong understanding of EVT, DVT, PVT, and Mass Production phase-gate methodologies, including pFMEA and process validation. Practical experience with QMS, CAPA, supplier quality management, and quality compliance for medical devices, preferably Class II or Class III products. Knowledge of relevant medical device standards and regulatory requirements, including FDA and ISO 13485. Proven ability to lead cross-functional projects involving yield improvement, cost reduction, process validation, and manufacturing efficiency. Strong analytical and problem-solving capabilities, including practical use of structured quality tools such as the 7 QC tools. Working knowledge of embedded systems and functional testing is an advantage. Ability to collaborate effectively across Manufacturing, Mechanical Engineering, Electrical Engineering, Quality, Supply Chain, Product, and Contract Manufacturing teams. Strong ability to simplify complex technical issues and communicate them effectively to non-technical stakeholders. Self-driven, proactive, adaptable, and comfortable working in a fast-paced and dynamic environment. Willingness and ability to travel regionally as required. Proficiency with Google Workspace and Slack is preferred. Knowledge or experience in AI and CAD is an added advantage. Fluency in English, Mandarin Chinese, and Malay is required, both written and verbal. Originally posted on Himalayas

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为什么有些职位使用英文?

职位名称和描述由招聘企业撰写。为避免改变招聘要求或工作条件,我们保留原文。操作界面和本指南使用简体中文。如果中文搜索没有结果,可以尝试使用职位发布语言中的名称或技能,例如“software engineer”。搜索词不会自动翻译,界面语言也不代表企业要求的申请语言。

远程职位是否允许从任何国家工作?

不一定。企业可能对居住国家、工作许可或工作时段有要求。请查看原始招聘页面中的具体条件。如果未说明,应先向企业确认,再判断能否从你所在的地区工作。“远程”标签本身并不代表没有地点限制。

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尝试更通用的职位名称或单个技能,并逐一移除筛选条件。不同企业可能用不同名称描述相似工作。如果某个职位已经消失,请在企业招聘页面搜索其职位编号。扩大搜索范围不会让已经关闭的职位重新开放。

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申请按钮会打开外部网站。请按照企业或招聘服务的说明,在该网站完成并确认提交。在 ResumizeAI 中准备简历并不等于已经申请职位。如果链接只打开企业网站,请先找到对应职位,再继续申请流程。

如何针对职位调整简历和求职信?

将招聘要求与能够解释清楚的项目、任务和成果联系起来。突出相关经历,不要添加未经实际掌握的技能或虚构成绩。在求职信中用具体例子说明申请动机,并遵守企业要求的语言和文件格式。提交前检查两份文件,确保内容准确、联系方式正确、链接可用。