「AVQ10 車載SQE主管」的相似工作

1.廠級相關Project, Lead導入與執行 2.配合公司相關品質政策活動之稽核 3.品質異常或客戶回饋問題之改善成效確認 4.執行製程稽核與品管檢驗工作 5.各種品質報表之填寫及稽核 6.ISO相關品質系統維護與執行 7.品質相關活動推展與品質改善活動專案執行 8.品管作業規範執行與稽核

需具備 科技／電子/通訊零組件相關產業經驗: 1. RMA、客訴處理, 客戶端異常回饋的問題釐清、調查、分析與矯正預防措施之擬定。  2. 主導供應商與外包廠商之品質監督、品質異常處理。 3. 供應商輔導與稽核, 品質系統監督及ISO文件優化。 4. 制定產品檢驗規劃以及產品功能之測試與驗證、製程品管問題的分析與改善。   5. 主導廠內、供應商、客戶端反饋 品質問題會議召開。  6. 公司品保(ISO 9000, TS16949, ISO 27001, QC080000...)等系統的建置, 維護與改善。 7. 產品可靠度驗證方案的制定與執行。 8. 帶領團隊完成工作目標。 9. 主管交辨事項。

1.品質稽核與流程優化 協助或主導總部現場稽核、品質稽核及審查(ISO 9001、IATF 16949、ANSI/ESD S20.20、ISO 13485 )，並且定期檢視並改善內外部品質系統及標準作業程序（SOP）以及優化NPI客戶品質需求文件。 2. 客戶品質對應與異常處理改善 主導重大客訴案件之調查、根本原因分析（RCA），推動內部改善對策（如製程優化、檢驗強化），編寫並提交 8D / 5Why / Fishbone 等問題分析報告，必要時需出差支援海外廠相關品質議題。 3. 品質目標監控與提升 制定並監控課內各項指標，分析達成進度並推動相關改善行動，提升部門績效管理。 4. 推動 ESG 專案 主導公司 ESG 相關工作，包括產品碳足跡的盤查、碳排放數據的收集與分析、碳減排目標的設定與落實，支持公司永續發展戰略。 5. 主管交辦事項的執行 協助完成主管交付的各項工作，並靈活應對部門其他臨時需求。

工作職掌: Pro QC 提供第二方稽核服務，透過對供應商進行適當的稽核，紀錄實際稽核結果並反饋給客戶。稽核員在事前需詳讀英文版之稽核文件與相關規範，稽核完成後提交英文報告。 技能與資格: 1. 執行 ISO 9001:2015稽核，具現場稽核經驗，有稽核員證照者尤佳 2. 撰寫英文報告 所需工作經驗: 5年以上工作經驗

1.全面負責品質保証部的工作管理，含蓋範圍： 進行檢驗管理、 巡迴檢驗管理 成品檢驗管理、 出貨檢驗管理、 供應商管理、 異常分析校正與矯正措施追踨、 產品失效分析與可靠度分析 2.負責公司保品體系建立並規劃品質系統相關教育訓練 3.主導內部稽核活動及外部認証 4.建立品質改善機制與品質改善活動推行 5.客訴管理 6.主導客戶定期品質相關會議

1. 年度品質目標的規劃與執行。 2. 生產製程品質的監控與不良的專案改善。 3. 品質異常與客戶抱怨處理,提高客戶的滿意度。 4. 測試實驗室的管理。 5. 品質成本的分析與改善。 6. 主管交辦事項。

【職務內容】 1. Customer service, audit, complaint handling 2. Supplier quality management, AR tracking 3. CIP, Eng project handling 4. GP, SOP, Quality contract review 【其他條件】 1. 五年以上半導體前 / 後段製程 2. 熟悉DRAM、WLCSP、2.5D/3D packaging process 3. 熟悉品質可靠度驗證、失效分析、FMEA 4. 曾服務國際大廠, 具英文簡報能力 5. 具主導專業經驗者尤佳

【COMPANY INFO】 Alarm.com is the leading cloud-based platform for smart security and the Internet of Things. More than 7.6 million home and business owners depend on our solutions every day to make their properties safer, smarter, and more efficient. And every day, we’re innovating new technologies in rapidly evolving spaces including AI, video analytics, facial recognition, machine learning, energy analytics, and more. Alarm.com is an Equal Opportunity Employer. In connection with your application, we may collect and use personal information (e.g., name, contact details, identification numbers, employment/education history, demographic and background check data) for recruitment, evaluation, compliance, and recordkeeping purposes. By applying, you acknowledge that certain data may be retained for internal operations and legal compliance. Alarm.com (ADC) seeks experienced and knowledgeable Manufacturing Quality Engineers responsible for managing manufacturing quality on-site at ADC's manufacturing partner's factories. In this role, you will act as the key interface on all aspects of the manufacturing quality, including IQC, IPQC, OQC, OBA, GRR, ORT, and CQI, between the Manufacturing Director and our manufacturing partners. You will conduct necessary manufacturing quality audits to ensure the manufactured products meet the ADC's quality requirements and manufacturing processes. Having deep technical understanding of manufacturing processes and practical experience in quality issue investigations, QA/QC practices, and supplier quality management are essential for success. 【Responsibilities】 · Follow the instructions from the Manufacturing Director to audit the executions per SIPs for IQC, IPQC, OQC and to conduct quality controls per SIPs for OBA, GRR, ORT and CQI. · Take the instructions from the Manufacturing Director to perform quality validation procedures for SMT, DIP and FATP. · Report to the Manufacturing Director on reviewing SCARs for component suppliers and 8Ds from manufacturing partners, implement quality training programs and/or additional quality requirements based on 8Ds, and track SCARs and 8D for continuous component and manufacturing quality improvement. · Gather historical manufacturing quality data to compare current with historical trends. · Compile manufacturing partner's quality performance based on the manufacturing quality metrics provided by the Manufacturing Director. · Assist the review of SCARs for component suppliers and 8Ds from manufacturing partners, implement quality training programs and/or additional quality requirements based on 8Ds, and track SCARs and 8D for continuous component and manufacturing quality improvement. · Work with manufacturing partners on analyzing the source of cause for material quality issues and drive for improvement from issue owners to ensure production running smoothly and efficiently. · Support Manufacturing Director and work with Product Managers to review RMA claims from customers, to conduct root-cause analysis with the manufacturing partners, and to drive the corrective resolutions as part of the overall improvement plan. · Work with Manufacturing Test Engineers and Production Engineers to validate and to ensure the manufacturing environment and production setup across the entire production system at all manufacturing sites are established and maintained according to the same quality standards. · Team up with Production Engineers and manufacturing partners to monitor on-going production quality and to continuously improve manufacturing quality including that of product assembly, test setup, and testing environment. · Support Production Engineers on manufacturing process simplification, optimization and standardization to achieve stable production lines with high quality yields.

1. 負責ISO 13485品質管理系統運作及其有效性。 2. 負責ISO 14001環境管理系統運作及其有效性。 3. 主導內、外部稽核及TFDA QMS 查廠。 4. 負責維護醫療器材許可證 (外銷專用許可證) 。 5. 負責客戶產品規格最終的審查與承認。 6. 負責維護產品法規符合性。 7. 醫療器材相關法規更新評估 8. 上市後監督報告彙整 9. 溫室氣體盤查報告彙整 10. 主管交辦事項

1.負責計劃、指揮及協調有關品質系統、品質保證、品質驗證、客訴問題處理等活動及部門日常管理。 2.負責維護公司品管系統，對各種生產品質問題進行追蹤處理。 3.改善產品信賴度、可靠性、品質，進而全面提升產品品質。 4.主導內部稽核活動及外部認證。

1 原物料相關事宜與異常處理. 2 供應商管理(考核/風險評估/客戶稽核等事宜). 3 ISO 9001/VDA 6.3/SONY GP/RBA 內外部稽核員. 4 人員教育訓練(內部/供應商) 5 供應商與有害物質相關系統推動與執行 6 上級交辦事項.

1. Customer quality interface 2. Drive NPI/MP quality improvement 3. Quality issue tracking and reporting 4. Manage quality PM

1. 負責建立並維護品質管理系統（如：ISO 13485、QMS、GMP）之相關文件，確保品質管理之有效施行。 2. 負責管理QMS文件系統，包含品質手冊、SOP、偏差管理及CAPA管理。 3. 主責年度國內外稽核審查（如 NMPA、FDA、CE）、客戶及供應商審核。 4. 監督和審核生產過程中品質控管的相關作業，確保其符合產品技術要求與法律法規。 5. 負責執行內部稽核、管理評審。 6. 協助原料、物料及成品檢測。 7. 協助QC依SOP執行產品檢測，包括理化檢驗、微生物檢驗或功能檢測。 8. 協助檢驗儀器的日常校驗、保養、紀錄及異常分析處理。 9. 與相關單位協辦不良品處理，及後續品質數據統計、抽樣計劃與分析。 10. 操作各類實驗儀器和設備，如滅菌鍋。

帶領產線品檢員團隊： 1.重大產品異常處理 2.iQC、IPQC、OQC管理 3.QC相關教育訓練及稽核 4.廠內品質目標及相關計畫執行

本職務為品管人員管理幹部，為常日班管理職，需帶領30~50位員工（台灣籍、菲律賓籍) 1.人員管理、調度、訓練與考核 2.各項品質指標追蹤、管制與改善 3.工作流程分析(ECRS)改善、成本降低與管控 4.專案規劃、改善與執行 (自動化、AI) 5.熟稔工業工程手法、具數理邏輯與程式撰寫能力、系統模擬、巨量資料分析者佳。 (E.g. Python, VBA, VSM, Flexsim, Tableau, deep learing...etc.) ＊實際薪資依學歷、科系、相關工作經驗、專業證照、特殊專長與語言能力綜合核敘 ＊資深人員薪資另議

1. 具半導體產業或CNC加工產業，製造或品保5年以上經驗 2. 須具備基本英文口說能力

1.新供應商品質管理系統評鑑 2.供應商品質系統評核及監控 3.供應商製程管控稽核 4.供應商品質異常分析、檢討及改善成效追蹤 5.必要時，陪同客戶至供應商處稽核 6.針對供應商的品質議題，作海外工廠＆台灣母公司的連繁窗口 7.協助海外工廠 IQC & SQE 人員的訓練&訂定相關的作業要求

1. 品質問題監督與管理(IQC/IPQC/FQC/OQC等過程)，異常反應處理及追蹤 2. ISO管理系統相關程序及文件維護、制定 3. 所需表單資料規劃，如: 品質檢驗表、檢測數據記錄表等 4. 品保人員工作職掌分配、品保系統作業標準化 5. 持續改善品質管理流程 6. 新物料規格確認、審核、承認 7. 主管交辦事項

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.)

Summary/Objective QMS: Implement the ISO quality system and procedure in the TDC plant to achieve the quality OD% and DPPM targets set up by corporate.                                            Essential Functions/ Responsibilities. 1. Working with management team to develop quality VMOST strategic plan and set up annual goals. Build strong implementation plan and monitor to ensure quality target achieving and sustain.                             2.Provides guidance and training to staff, assists subordinates in attaining career goals, motivates individuals to achieve results, and recruits and maintains a high-quality staff.                             3. Applies sound, systematic problem-solving and preventive methodologies in identifying, prioritizing, communicating, and resolving internal and external quality issues.                           4. Maintains ISO9001 program and quality assurance procedures to ensure customer requirements are satisfied throughout the TDC facility and at our suppliers.                               5. Lead all Quality in-house professional audits, coordinate customers/independent audits and oversees or performs audits to suppliers per the schedule                               6.Assure compliance to requirements and optimization of process capabilities to ensure product quality, customer service, and cost effectiveness.                                7. Control nonconformance both externally and internally. Initiate, implement and verify corrective actions as needed in the QP system.                             8. Using the QP data system to analyze manufacturing quality data and lead problem-solving activities.      9. Implement SPC and capability studies in the ITS system for process quality control .                    10.Leading the TDC Quality team to reduce customer complaints, customer returned values and quality cost.                                11. Proactive investigates, identifies, and implements quality procedures and work instructions;                12. Work with the management team to develop and setting up annual EMS objectives/targets and program to ensure the environment target achiving ans sustain.                                                      13. Plans, drills and reviews EMS emergency response                          14. Support and take part in EMS management review                                15. Take part in the EMS External audit                             “The responsibilities as defined are intended to serve as a general guideline for this position. Associates may be asked to perform additional tasks depending on strengths and capabilities.”  Required Experience  "With quality management experience 5years minimum experience."