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操作画面は日本語です。企業が掲載した求人の職種名や説明文は原文のまま表示され、英語の場合があります。

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Senior Manufacturing & Quality Engineer – Medical Devices & Consumer Electronics

MatchaTalent

リモート勤務

勤務地
Remote (Malaysia)
勤務時間
Full Time
掲載日
2026年10月10日

応募する前に、企業のウェブサイトで現在も募集中かどうかと詳しい条件を確認してください。

仕事内容

操作画面は日本語です。企業が掲載した求人の職種名や説明文は原文のまま表示され、英語の場合があります。

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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必須条件と歓迎条件を分けて確認し、勤務時間、報酬、勤務地が掲載されている場合は目を通しましょう。リモート勤務でも、居住国、就労資格、勤務時間帯が指定されることがあります。現在の募集状況と詳しい条件は企業に確認してください。

募集要件に関連する実際の経験を選び、自分の役割と貢献を説明しましょう。数値は根拠がある場合にのみ使ってください。企業の応募方法に従い、送信前に連絡先、内容、PDFの表示を確認しましょう。

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仕事探しに関するよくある質問

英語の求人が表示されるのはなぜですか?

職種名や説明文は企業が作成したものです。条件や要件を変えないように原文を掲載しています。操作画面とこのガイドは日本語です。日本語の検索で見つからない場合は、「software engineer」のように、掲載言語の職種名やスキル名でも検索してみてください。検索語が自動翻訳されるわけではありません。

リモート求人なら、どの国からでも働けますか?

必ずしもそうではありません。居住国、就労資格、勤務時間帯が指定されている場合があります。元の求人ページで条件を確認してください。記載がない場合は、自分の居住地から応募できると判断する前に企業へ確認しましょう。リモートという表示だけでは、勤務地の制限がないことは分かりません。

検索結果が出ない場合はどうすればよいですか?

より一般的な職種名や一つのスキルで検索し、条件を一つずつ外してみてください。同じような仕事でも企業によって呼び方が異なります。特定の求人が見つからなくなった場合は、企業の採用ページで求人番号を探しましょう。検索条件を広げても、終了した募集が再開するわけではありません。

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応募ボタンは外部サイトを開きます。企業または採用サービスの案内に従い、そのサイトで送信を完了してください。ResumizeAIで応募書類を作成しただけでは応募は送信されません。リンク先が企業のトップページの場合は、該当する募集を探してから手続きを進めましょう。

応募書類とカバーレターはどう調整すればよいですか?

募集要件と、自分が説明できるプロジェクト、業務、成果を結び付けます。経験していない技術や実績を加えず、関連する経験を分かりやすく示してください。カバーレターでは応募理由を具体例とともに伝えます。指定された言語とファイル形式に従い、送信前に両方の書類を確認しましょう。