「【生產製造類】生產製造主管-硬化劑」的相似工作

1. - Analytical Method Development: Perform analytical method development, formulation screening, finished product testing, stability study, dissolution testing, RLD reverse engineering, technical transfer, and laboratory-related work during the development stage. Support NDA and ANDA submission. Support the complete drug development lifecycle management. 分析方法開發- 主要職責包括以下內容: 在開發階段進行分析方法開發、配方篩選、成品測試、安定性研究、溶出度測試、原廠藥逆向工程、技術轉移和實驗室相關工作。協助NDA和ANDA查驗登記。協助完整的藥物開發生命週期管理。 - Method Validation: Perform analytical method validation, analytical method verification for drug substances, finished products, cleaning analytical methods. Conduct method transfer. Support raw material and stability analysis. Support NDA and ANDA submission. 方法驗證: 執行原料藥、成品、清潔分析方法的分析方法確校、分析方法確認。執行方法轉移。協助原料和安定性分析。協助NDA和ANDA查驗登記。 2. Train, lead, mentor and supervise team members in day-to-day laboratory operations. Support relevant departments and customers to complete projects on time. Ensure all activities and analysis comply with GMP, correct procedures, policies, and health and safety regulations. 在日常實驗室操作中，訓練、領導並監督團隊成員。協助相關部門和客戶按時完成專案。確保所有活動和分析均符合藥品良好製造規範、正確的程序、政策以及健康和安全法規。 3. Responsible and accountable for the quality and timeliness of the project deliverables, resource management, technical support for team members, and communication of the progress to the senior management. 對專案交付的品質和及時性，資源管理，團隊成員的技術協助以及與高級管理階層的進度溝通負責並承擔責任。 4. Manage and lead day-to-day operations with the team, including prioritization, task assignment, workload management, and risk management. 與團隊一起管理和領導日常運作，包括優先順序調整、任務分配、工作負荷管理和風險管理。 5. Adequately utilize and maintain analytical instruments/equipment. Diagnose and identify solutions to resolve analytical instrument issues. Perform calibration, qualification, and preventive maintenance. Support for procurement and qualification of new analytical instruments/software. 充分利用和維護分析儀器/設備。診斷和識別解決方案以解決分析儀器問題。執行校正、驗證和預防性維護。協助採購和驗證新的分析儀器/軟體。 6. Review the documents, electronic records. Prepare analytical protocols and reports, and CMC documents. Monitor data trending and support for deficiency letter response. Ensure good documentation practices and data integrity. 審查文件、電子記錄。準備分析計畫書和報告以及化學製造管制文件。監控數據趨勢並協助缺失信件回覆。確保優良文件化規範和數據完整性。 7. Lead and support CCR, deviation investigation, CAPA, LIR, SOP preparation, internal and GMP inspection。 協助變更管制、偏差調查、矯正預防措施、實驗室調查報告、標準操作程序準備、稽核。 8. Responsible for managing monographs, validated excel sheets, approved reports (paper and electronic), notebooks, and scan copies. 負責管理檢規、經過驗證的Excel工作表、已批准的報告（紙質和電子版）、筆記本和掃描副本。 9. Support assigned responsibilities to maintain GMP compliance of the chemical laboratory, as applicable. 如適用，依據分配責任，維持化學實驗室運作皆符合藥品良好製造規範。 10. Transfer analytical method to Quality control, QP sites, and other receiving laboratories. 轉移分析方法到品質管制，QP所在地和其他接收實驗室。 11. Lead and guide laboratory management work, e.g., reference/working standard management, instrument management, laboratory area cleaning, reagents and solvents, and other supporting systems. 領導和指導實驗室管理工作，例如參考/工作標準管理、儀器管理、實驗室區域清潔、試劑和溶劑以及其他支援系統。 12. Stay informed with the latest industry trends, techniques, and best practices. 隨時了解最新的行業趨勢、技術和最佳實踐。 13. Perform literature search, patent landscape review, regulation comparison, review guidelines, read the pharmacopeias, technical document to understand the latest knowledge of the pharmaceutical industry. 進行文獻檢索、專利態勢審查、法規比較、審查指南、閱讀藥典和技術文檔，以了解製藥行業的最新知識。 14. Ensure the laboratory Capex management. Review & approval 0f URS, DQ, IQ, OQ, PQ & Vendor qualification. 確保實驗室資本支出管理。 審閱和批准 URS、DQ、IQ、OQ、PQ 和供應商資格。 15. Promptly complete work and tasks assigned by the supervisor 及時完成上級下達的工作和任務。 16. Motivate and empower team members. Conduct performance review and appraisal for team members. 激勵和授權團隊成員。執行績效審查和評價。 17. Engage with the team and manage the conflict, making sure individual employees into a cohesive team and complete the project milestone. 與團隊互動並管理衝突，確保員工個人成為一個有凝聚力的團隊並完成項目里程碑。

倉儲員(2名): 1.負責產品接收入庫.出庫堆高機作業 2.倉儲系統銷存流程管理作業 3.倉庫庫存盤點管理作業 中班 19:00-05:30及21:00-07:30(需支援輪班) 休息時間0.5H 待優:底薪+津貼+輪津+加班費,上市公司福利。 *有堆高機者佳

此職務主要負責電鍍現場異常處理與化學藥液系統建立 工作職責包含: 1.貴金屬成本cost down專案規劃與執行 2.藥水測試與生產專案的執行 3.一般化學品與貴金屬點檢與複查 4.藥液管理系統標準建立與校正更新 5.化工同仁工作教導 歡迎對此職務有興趣者加入我們，非相關科系亦可

1.須接受公司輔導委外受訓取得相關證照。 2.負責生產線機器、設備之操作，維持正常運作負責產品包裝線管理。 3.執行與督導生產線環境清潔。 4.與同仁互助，達成生產目標。 5.需食品相關產業，任職3年以上資歷。 6.完成主管交辦事項。 應徵者須備妥 (供膳體檢合格報告)(食品相關科系者優先)

1.生產製程操作。 2.所屬設備之操作保養與維護。 3.責任區域負責、回報。 4.其它主管交辦事項。 5.需輪班。(小夜班夜點費240元/大夜班夜點費480元，另計)

1.半導體精密沖壓製程生產效率及良率監控 2.製程技術標準及生產流程建立(FMEA/CP/SOP) 3.產品品質異常改善 4.新產品製程能力評估及送樣 5.製程設備優化評估及導入 • 實際薪資及職稱依學歷、科系、相關工作經歷、專業證照、特殊專長與語言能力等條件綜合核敘

1.進行原物料、成品檢驗工作 2.執行儀器校驗 3.實驗室管理與藥劑配製

台灣瑞曼迪斯為德國最大的環保公司REMONDIS集團在台投資設立，專責所有環保相關產業，目前為未來發展策略進行擴編徵才，歡迎具備職務所需之專業技能的有志人士加入我們。 1. 規劃與執行生產排程，確保各產線運作順暢，並持續提升產線效率。 2. 掌控設備生產參數，適時調整以維持產品品質與穩定性。 3. 處理生產異常，調度現場人員及資源，快速恢復正常生產。 4. 負責團隊管理，包括人員排班、調配、培訓與績效考核，建立高效能團隊。 5. 確保人員遵循安全操作規範，並推動相關教育訓練。 6. 跨部門溝通與協調，確保生產流程順暢。 7. 掌握生產物料、輔料及耗材數量，執行請購及庶務作業。 8. 收集並分析生產相關數據，推動製程改善，降低不良率與生產成本。 9. 協助落實 ISO / EHS（環安衛）等管理制度，符合公司及法規要求。 10. 定期檢視部門績效，回報生產狀況與改善計畫予高階主管。

1. To establish training curricula in accordance with requirement of manufacturing activities, including manufacturing technology, GMP concepts and other working guidelines. 依照製造活動之需求建立訓練課程，包含製造技術、GMP概念與相關工作規範。 2. To establish wide variety of training materials, including SOPs, training slide deck, training video, testing questions and training checking list. 建立各種類型之訓練教材，包含SOP、訓練簡報、訓練影片、課程考題與訓練檢核表。 3. To optimize the current training materials, including revision of SOP, updating of slide deck and editing of training video. 針對現有的訓練教材進行優化，包含SOP改版、簡報更新與訓練影片製作。 4. To conduct effective induction and orientation sessions. 執行有效的新進人員培訓課程。 5. To conduct training activities in accordance with the training program, including newcomer training, SOP training, on-the-job training (OJT), and training activities related to GMP production. 依照訓練計畫執行訓練活動，包含新人訓練、SOP訓練、OJT與GMP生產相關之訓練活動。 6. Compile training document records and save them to training management system and assist in maintaining the training curricula in the training system. 彙整訓練文件紀錄保存至訓練管理系統並且協助維護訓練系統之訓練課程內容。 7. Other works assigned by manager. 其它主管交辦事項。

1.原料、成品之一般檢驗及微生物檢驗 ，以確保品質符合公司規範。 2.執行公司產品的可靠度測試，並分析問題，以找出造成產品可靠度問題的關鍵因素。 3.生產線巡檢、環境監控及機具設備衛生檢查 。 4.檢測數據統計、分析與資料歸檔 。 5.執行內部衛生稽核 。 6.具有HACCP(Hazard Analysis Critical Control Point 食品衛生安全重點控制) 60A、60B證照者，優先錄取。 7.其它主管交辦事項。

歡迎加入我們拓展您在化工廠的操作經驗，我們有多樣的化工製程操作單元、壓力容器操作並盡可能使用堆高機、固定式起重機等機具輔助貨物運送減少勞力負荷、改善人體工學。 依照生產工單需求，設置好生產設備及材料，並安全、有效率地完成生產流程 -遵照安全及操作相關SOP以及公司政策，例如穿戴必須的個人防護具進行生產操作 -具備危害鑑別意識並回報不安全的操作情況 -完成生產組長的任務安排 -生產問題疑難排解並適當溝通 -熱心地協助及指導新進同仁 -樂意分享並提出可提升安全及操作效率的改善建議 -維持安全、整潔的工作環境

1.執行ISO國際認證 (例如:ISO 9001、14001、45001、50001…等等) 2.執行供應鏈稽核 3.執行品牌認證稽核 4.化學品管理 5.碳排放管理 6.主管交辦事項

1.負責焚化爐、公用系統（鍋爐、冷卻水、壓縮空氣、RO純水、空調等）之運轉監控與技術支援，確保系統穩定運行並符合法規要求。 2.評估與優化公用系統操作條件，提升能源效率、設備稼動率及資源利用率。 3.主導環保設施（如廢水處理、廢氣洗滌系統）操作策略與改善專案，降低排放風險。 4.建立並維護日常巡檢、點檢表與設備操作標準作業程序（SOP），強化預防性維護及異常管理機制。 5.協助規劃耗材管理與副產物處理流程，提升作業效率與安全性。 6.分析公用系統營運數據與異常記錄，導入製程優化與改善計畫。 5.支援設備異常調查、故障排除與異常根因分析（RCA），並提出對策建議。 7.執行安全作業與風險控管措施，配合環安衛及工務單位進行稽核與改善。

1.負責生產製程管制與人員調配。 2.確實執行生產目標，並達成各項生產指標。 3.生產進度跟催及異常排解 4.進行跨部門溝通協調。 5.負責人員培育與績效考核。

1. Establish, implement, and maintain quality management systems (e.g., ISO 9001) for electronic chemical products 2. Handle quality incident investigations, root cause analysis, and corrective/preventive actions (OCAP) 3. Collaborate with R&D, production, and sales teams to improve overall quality performance 4. Manage customer audits and respond to third-party inspections 5. Monitor and improve raw materials, in-process, and finished goods quality 6. Group-wide Implementation of Statistical Process Control (SPC)

※ 本職務需具紡織工廠管理經驗，其中至少 5 年染整工廠高階主管管理經驗，熟悉染整、生產製造技術與流程，及各項廠務規劃管理。（未具備上述經歷勿投履歷） 在州霖，你不只是工廠管理者，更是品質、效率與交期的掌舵者。全面統籌營運，從生產規劃、品質管控、機台維護，到人員調度，精準執行每一道工藝，確保每批產品準時交付。面對開發與大貨挑戰，帶領團隊快速應對；針對客戶品質反饋，深入分析並提出改善方案；同時掌握產能與交期，協同生管系統化優化流程，推動整體營運效能。 【工作內容】 1.《現場作業管理、規劃》　　： 制定並落實生產規劃，確保現場運作順暢 2.《製程改善、生產效率提升》： 主導製程優化與成本降低，持續提升效率 3.《環安衛與標準作業管控》　： 符合環安衛規範；協助產銷平衡品質與交期，嚴管 SOP 4.《生產排程與交貨品質管理》： 管控排程與產能，準時交付並達成品質與產出指標 5.《產線異常排除、分析》　　： 立即處置產線異常，並追蹤根因，確保生產不中斷 6.《幹部領導與員工培訓》　　： 帶領幹部、推動溝通與督導，執行績效管理與人才培育 7.《內部稽核、外部認證管理》： 主導內稽並監督外部認證，符合歐美相關國際標準 8.《效益分析、改善策略報告》： 進行效益評估，提出並追蹤改善方案，破除瓶頸 9.《績效指標設立、定期考核》： 與管理層訂定各部門 KPI，定期檢核並確保目標達成

1. synchronize in-time information to both design and manufacturing team and make sure cross function team on the same page. 2. provide mitigation plan with cross function team when facing manufacturing/material/capacity issues. 3. work with factory team to achieve shipment target from NPI to MP phase. 4. work with engineering team/process team to solve manufacturing issues. 5. work with material/buyer team to ensure material delivery 6. work with process engineer/production planner to ensure production capacity

[ABOUT THE ROLE] The Manager, Manufacturing Engineering is a key manufacturing leadership role within Peloton Taiwan/Asia Region. You will work in a cross-functional environment (mechanical engineering, manufacturing, quality and program management) with the responsibility to provide technical and developmental leadership for a team of manufacturing engineers involved in the production system design, start up, ramp, and operational support efforts. You will lead in a variety of tasks including, but not limited to, hiring, coaching, development, performance reviews, project planning, execution, and resource allocation to deliver performance oriented work to be completed. This person will improve operational efficiency of the CM (Contract Manufacturers) through line output enhancement and the elimination of all forms of loss and waste. The Senior Manager, Manufacturing Engineering will also partner with CM/JDM/ODM on manufacturing resource planning, cost reduction initiatives, product running change implementation, and resolving production issues. The engaging attitude towards manufacturing issues with problem-solving determination is a plus for acting on this role. [YOUR DAILY IMPACT AT PELOTON] - Lead a team of Peloton manufacturing engineers in a fast-paced, CM/ODM/JDM environment with an inclusive culture of integrity - Collaborate with CM/ODM/JDM in identifying and qualifying suitable manufacturing processes; Identify and highlight manufacturability issues during pre-production builds to ensure product quality is stable and that supply is predictable during ramp and regular activities to ensure manufacturing performance - Manage local manufacturing engineering activities including resource planning, project management activities and implementation of manufacturing equipment, systems, and processes - Collaborate with internal and external cross-functional teams including Product Managers, Industrial Design, Mechanical Engineers, Quality, Sustaining, Operations and Logistics to deliver Peloton products to market - Drive the supply base to ensure high-quality, predictable manufacturing activities - Lead Focused Improvement activities in the plant with primary actions to drive improvements through lean manufacturing techniques - Identify opportunities for continuous improvement initiatives involving daily operations, engineering/assembly in-processes and organization structure - Utilize cost deployment to identify areas with the most opportunity, then leading teams through projects to resolve and reduce the losses, and leading development of the management team - Experience in hands-on manufacturing, assembly environment and consumer hardware assembly experience preferred - Knowledge of component, assembly, schematics, engineering drawings - Knowledge of various manufacturing processes, including CNC machining, injection, overmolding, welding, and metal forming, etc.

1. 統籌新產品導入生產的相關事宜。 2. 負責例行性製造生產作業與產線人員管理。 3. 確實執行生產目標，並達成各項生產指標。 4. 倉庫管理。 5. 維持品質管理系統運行。

(1)依公司策略發展所需，規劃生產部功能發展，並指導所屬部門年度預算之編擬與執行。 (2)生產效能、產值、品質及人力狀況審查與控管 (3)生產流程自動化規劃 (4)生產品質改善提升規劃 (5)生產重大異常管理，如製程品質異常、重要設備、工安事故等。 (6)生產廠區運用規劃。