「【R&QA】供應商品管(資深)工程師 (SQE)」的相似工作

主要職責 : 1)管理供應商出貨品質 2)執行供應商品質稽核及輔導改善 3)客戶及製程材料不良分析及後續追蹤改善 4)品質資料統計分析 5)品檢員訓練計劃擬定及實施 6)檢驗儀器設備教育訓練 7)建立材料檢驗品質標準

1. New supplier survey and existing supplier audit 2. Support special task related to supplier quality management (ex. onsite supporting and deal with urgent supplier quality issue and yield). 3. For key supplier material quality reviewing and driving improvement a. VLRR/LRR review b. Deal with supplier issue continuous improvement plan. c. SCAR review d. Supplier process audit/review 4. Assigned task supporting (ex. MQC CAMP system maintenance, defective material cost task force, procedure revising.)

We are looking for an exceptional Supplier Quality Engineer (SQE) to join our global team. As an SQE, you will play a critical role in developing, qualifying, and managing suppliers to ensure the highest quality standards and drive continuous improvement initiatives. This position requires effective resolution of supplier quality issues and collaboration with suppliers to develop a strategic career in a dynamic, multinational environment. 我們正在尋找優秀的供應商品質工程師（SQE） 加入我們的全球團隊。 作為 SQE，您將在開發、認證與管理供應商方面發揮關鍵作用，確保最高的品質標準，並推動持續改進計劃。該職缺需要有效解決供應商的品質問題，並促進與供應商的合作，在動態的跨國環境中發展戰略性職業生涯。 Key Responsibilities: • Supplier Management: Establish and maintain strong relationships with suppliers to ensure the quality and reliability of materials and components. • Quality Assurance: Conduct supplier audits, process validations, and quality assessments to meet international standards and company requirements. • Problem Solving & Continuous Improvement: Lead root cause analysis and corrective actions using effective problem-solving tools such as 8D, 5-Why analysis, and FTA. • Cross-Functional Collaboration: Work closely with internal teams including Procurement, R&D, Engineering, and Operations to align supplier performance with business objectives. • Compliance & Quality Standards: Ensure supplier compliance with ISO, IATF, or other relevant quality standards and regulatory requirements. • On-Site Visits & Audits: Conduct on-site supplier evaluations, production monitoring, and quality improvement projects. • Strategic Growth: Provide insights into supplier capability development to support long-term sourcing strategies and business expansion. 主要職責： • 供應商管理：建立並維持與供應商的良好合作關係，確保材料與零件的品質與可靠性。 • 品質保證：執行供應商稽核、製程驗證及品質評估，以符合國際標準及公司要求。 • 問題解決與持續改善：運用有效的問題解決技術（如 8D、5Why 分析、FTA 等）主導根本原因分析與矯正行動。 • 跨部門合作：與採購、研發、工程與營運等內部團隊密切合作，使供應商表現與業務目標一致。 • 法規遵循與品質標準：確保供應商遵守 ISO、IATF 或其他相關品質標準及法規要求。 • 現場訪查與稽核：實地供應商評估、生產監督及品質改善專案。 • 策略成長：提供供應商能力提升的見解，支持長期採購策略與業務拓展。

按讚並追蹤"台達Delta Career"FB粉絲專頁，讓您更快掌握台達職缺脈動！ https://www.facebook.com/deltacareer 1. 協助材料品質改善目標的執行。 2. 協助產線及市場反饋之原物料異常分析、解決與追蹤。 3. 協助原物料品質提升專案執行。 4. 參與協助供應商及外包商評鑑、稽核與輔導。 5. 吳江/泰國工廠SQE團隊, 流程與做法整合 6. 年度sourcing plan制訂與執行 7. 協助吳江/泰國年度稽核計畫排定並確認執行度 ※必要條件：具備半導體相關經驗，了解主被動元件材料※ ※加分條件：具備IATF16949品質系統概念※ ※歡迎具備半導體相關經驗(1~3年)求職者投遞※

負責供應商電子件管理品質工程師 1. 依據所負責電子件的品質管控重點，制定相對應的SIP/MSOP並指導機構件進料檢驗員，相關檢驗重點要求 2. 新供應商評估/舊供應商品質稽核與輔導 3. NPI階段Key parts物料相關管制點建立 4. 製程/客戶端異常反饋供應商執行改善對策及追蹤考核 5. 經由數據收集跟分析，當品質不良率逐漸上升，需即時採取改善對策，持續提升品質 6. 供應商品質改善專案

SQM工程師 1.供應商生產及系統稽核、輔導、評鑑。 2.協助採購對新供應商評估及稽核。 3.確認供應商品質異常處理及改善對策、報告跟催。 4.使用游標卡尺、量測設備等，把關產品的規格尺寸。 5.曾任職供應商管理相關職務者佳。 ＱＥ工程師 1. 樣品到量產整個生產過程的產品監控。 2. 產品生產過程中異常處理及品質改善。 3. 制訂各種與品質相關的檢驗標準。 4. 客訴處理、改善報告撰寫與回覆客戶報告。 5. 使用游標卡尺、量測設備等，把關產品的規格尺寸。

▼封裝領導廠▼ [產品服務：功率模組封裝─Hybrid、RF、Power] 1、處理客戶訴怨。 2、製程異常的反應及處置。 3、監控量產產品良率及品質。 4、客戶稽核的準備及結案追蹤。 5、客戶溝通及協調。 *工作待遇/職稱：將依學經歷及專長等條件進行敘薪。

1.產品開發規格與檢驗標準建置（IPQC 對接） 負責產品開發階段的品質規格與檢驗標準建立與審查，並將相關檢驗項目整合進入IPQC流程，確保設計品質於初期即受控。 2.製程規範審查與風險評估管理 建立並審查產品製程相關作業規範，進行風險分析（如PFMEA），針對潛在失效點擬定預防對策，並追蹤矯正單位（LED）改善進度。 3.製程變更（ECN）管理與流程整合 主導產品製程工變流程，確保變更內容符合品質與製造規範，並整合橫向流程與部門協作，提升製程彈性與一致性。 4.客戶聲音（VOC）整合與根因分析驗證 彙整來自客戶端或市場的品質回饋，進行問題歸類與根因分析，並主導跨部門改善方案的驗證與落實，強化客戶滿意度。 5.CAPA 系統管理與改善行動落實 負責品質異常或客訴事件的CAPA管理，從VOC中萃取改善機會，規劃矯正／預防行動，追蹤實施進度與驗證改善成效。

1.車載機構料件品質異常處理 2.供應商品質改善措施審核及改善效果追蹤 3.供應商稽核及異常改善措施落實度確認 4.重要料件PPAP的資料收集 5.改善提升供應商管理能力，提升客戶滿意度 6.客戶抱怨之處理與預防 7.承接及執行主管派任的特殊任務

1. 新產品NPI階段試產結果的確認及問題改善跟催 2. NPI階段組裝與測試設備的設計與驗證 3. 新產檢驗及測試標準制定 4. 供應商現場稽核 5. 供應商品質管制與評鑒 6. 製程品質稽核與改善效果追蹤 7. 客戶/專案品質管理與改善 8. DOA/RMA的品質改善與追蹤 9. 熟悉TS16949五大工具，SPC/ FMEA/ PPAP/ MSA/ APQP 10. 客訴問題的報告與回復 11. 客戶專案進度掌控/定期與客戶會議

【本職缺僅接受穩懋官方網站投遞】請至穩懋官方網站投遞個人履歷表，此職缺履歷登錄網 https://www.winfoundry.com/WinTalentPool/JobRequirement/Edit/706 1. Inline performance analysis and review. 2. Cowork with Fab for inline performance improvement 3. SPC audit and training 4. Issue customer related and technology release stage SPC report 5. Project assist

1.ISO文件維護、審查相關管理作業 2.集團品質KPI 數據彙整分析 & 專案執行 (需有Excel統計分析 & IATF 16949 經驗) 3.品質/SAP 週月報之彙整 (需具備簡報製作能力)

1. 負責建立進料檢驗標準, 品管相關文件制修訂與維護。 2. 確保各項品管檢測方法及方法適用性。 3. 定期彙整供應商品質/進料品質統計報告，週期性檢討進料檢驗規範與抽樣計畫，持續改善來料品質。 4. 原料、半成品、成品因原材料異常分析/判定。 5. 供應商進料缺失矯正與預防。 6. 管理輔導、稽核與評鑑供應商品質，定期或不定時召開供應商品質檢討會議。 7. 協助執行內部稽核與對應外部稽核作業。 8. 其他主管交辦事項。

1. 處理供應商提供的物料品質異常問題，並跟進改善。 2. 供應商的8D Report回覆確認與管理。 3. 制定並監控供應商品質檢驗規範。 4. 產線來料不良項目反映受理。 5. 每月供應商品質評比與等級評鑑。 6. 供應商換貨及折讓管理。 7. 年度定期或不定期對供應商進行品質稽核。 8. 每日料況巡檢/即時狀況反映供應商。 9. 委託外部實驗室測試安排。 10. 對於機構料與電子料有相關經驗。 11. 主管交辦事項。

1.客戶品質窗口，協助提供生產相關品質報告 2.具跨部門溝通能力，需與他部門人員完成客訴8D報告的撰寫 3.品質良率改善專案的參與

1. 規劃與執行品質管理體系 2. 監督與管理品質保證團隊 3. 確保產品品質符合標準 4. 持續改進品質管理體系

1、品質客訴異常處理：確認客戶抱怨異常、不良品分析、品質客訴8D報告 2、與製造地CQA串聯、主導TW廠客訴和相關單位溝通協調 3、客訴履歷分析彙整 ＊*＊實際薪資將依學經歷及相關工作核定*＊＊

SHL Medical is the world-leading solution provider in the design, development, and manufacturing of advanced drug delivery systems with more than 5000 employees worldwide. Our customers include top pharmaceutical and biotech companies from around the globe that require innovative devices such as auto injectors or pen injectors to effectively deliver their drugs. Headquartered in Switzerland since late 2018, with sites in Sweden, Taiwan, and the Unites States. 【Job Overview】 The Supplier QA Engineer is responsible for • To drive supplier quality performance, including new product development and product quality improvement • Overseeing supplier quality and establishing quality control objectives • Ensuring the supplier fulfill regulatory and SHL’s requirements • Performing quality system audits and development good partnership with suppliers 【Main Responsibilities】 • Ability to manage the quality of products and services provided by suppliers, ensuring compliance with company standards and requirements. Independently conduct investigations on abnormalities, analyze potential process risks, identify root causes, and drive improvements to continuously enhance supplier quality performance. • Experience in planning and executing supplier evaluations and audits, including document reviews and on-site inspections. Coordinate and support second-party and third-party certification audits. Evaluate supplier responses to deficiencies and lead supplier quality improvement initiatives. • Familiarity with quality management systems and relevant standards (e.g., SOPs, GMP). Capable of developing and maintaining quality documents and training programs. Provide quality and GxP training to internal teams and suppliers to ensure audit readiness. • Skilled in data analysis to drive continuous improvement projects aligned with departmental and company goals. • Strong communication and coordination skills to effectively collaborate with cross-functional teams and suppliers, resolve quality issues, and report quality status and audit findings to senior management. • 具備管理供應商產品及服務品質的能力，確保其符合公司標準與要求。能獨立展開異常調查，分析製程風險，找出根本原因並推動改善，促使供應商持續提升品質表現。 • 能規劃與執行供應商評估及審核，包括文件審查、現場稽核，以及協助安排第二方與第三方認證稽核。能評估供應商缺失回應並帶領品質改善計劃。 • 熟悉品質管理系統及相關標準（如SOP、GMP等），能制定及維護品質文件與培訓計劃，並提供內部與供應商的品質及GxP培訓，確保稽核準備度。 • 擅長運用數據分析推動持續改善計劃，以達成部門及公司目標。 • 具備良好的跨部門及供應商溝通協調能力，能有效解決品質問題，並能向高層管理者報告品質狀況與稽核結果。 【Qualification】 • A bachelor's degree in engineering, manufacturing, technology-related fields or other science-related fields is required. • At least three years of experience in quality assurance, preferably in the medical device, biopharmaceutical, or other regulated industries. • Familiarity with 21 CFR part 820, ISO 13485, and cGMP is a plus. • Internal audit training in ISO 13485 / ISO 9001 or equivalent is a plus. • Experience managing external quality audits is a plus. • Familiarity with quality tools, audit techniques, and problem-solving skills is a plus. • Ability to collaborate well within a cross-departmental team and independently manage workload. • Good interpersonal, written and verbal communication skills in both English and Chinese. • 具備工程、製造、技術相關或其他理工科相關領域的學士學位。 • 至少三年以上品質保證相關經驗，醫療器材、生物製藥或其他受規管產業經驗者優先。 • 熟悉21 CFR Part 820、ISO 13485及cGMP者佳。 • 具備ISO 13485 / ISO 9001內部稽核培訓經驗者優先。 • 具管理外部品質稽核經驗者佳。 • 熟悉品質工具、稽核技巧及問題解決能力者優先。 • 能良好協作跨部門團隊，並具備獨立管理工作負荷的能力。 • 具備良好的人際關係、中文及英文書面及口頭溝通能力。

▼封裝領導廠▼ 晶圓重組、晶圓/成品測試&生技醫療產品封裝、通訊模組封裝─Bio、RF 1、執行製程/產品稽核彙整及呈報。 2、推動製程持續改善(SPC監控、ESD相關、有害物質管理)。 3、內部異常跟催與有效性確認。 4、跨部門合作。 5、主管交付專案。 * 工作待遇/職稱：將依學經歷及專長等條件進行敘薪。

Your Job As a AQP Engineer at Molex, you won’t just own deliverables — you will drive results. This role demands a strategic thinker who thrives on identifying risk early, influencing cross-functional teams, and bringing structure and confidence to new product launches. You’ll lead from the front across engineering, manufacturing, and quality functions — guiding Molex's New Product Introduction (NPI) projects toward excellence in both technical performance and economic efficiency. Your success is measured not just by launches on-time, but by the quality and resilience of the product and process behind them. Our Team Advanced Quality Planning (AQP) What You Will Do 1. Be the bridge between customer requirements and technical execution, driving engagement across PM, PJM, MIE, Product Design, and PE teams to align expectations and embed the voice of the customer (VOC) in every stage of product development. 2. Champion risk-based thinking using tools like DfM/A, D&PFMEA, Control Plan, and MSA. Your role is not to check boxes — it’s to ask bold questions, challenge assumptions, and remove roadblocks to success. 3. Lead AQP performance in the Copper Solutions Business Unit (CSBU), ensuring critical projects meet quality, timing, and launch readiness goals. 4. Guide execution of Molex’s PDP (Product Development Process) framework to anticipate problems before they happen, and build repeatable, robust systems. 5. Own product qualification documentation, ensuring external approvals are achieved without rework or delay. 6. Lead NPI-stage process audits and drive real closure of findings. 7. Quantify and attack Cost of Poor Quality (CoPQ) early in the product lifecycle. 8. Continually improve AQP practices, from both technical and workflow perspectives. 9. Be a cultural driver — modeling PBM values like Principled Entrepreneurship, 10. Self-Actualization, and Transformation. Use economic thinking to guide technical choices with business impact. Who You Are (Basic Qualifications) 1. Bachelor’s degree or above in Mechanical Engineering or a related field. 2. Minimum 2 years of hands-on experience in Product Development, Quality Engineering, or Manufacturing Engineering. 3. Skilled in problem solving tools: SPC, PDCA, 3-Legged 5 Why, Shainin, Ishikawa, and MSA (experience with Minitab a plus). 4. Influence without authority. You ask “what’s the tradeoff?” and help others make risk-adjusted decisions. 5. Comfortable communicating in English — both written and spoken. P6. assionate about Transformation. You challenge status quo to find a better way.