轉職熱搜工作

1.主導永磁同步馬達（PMSM）及無刷直流馬達（BLDC）的驅動系統開發案，包含功率電子、電源管理、驅動電路 及磁場導向控制（FOC）、六步換相控制等產品實現。 2.熟悉DC-DC、AC-DC電路設計，包括逆變器、功率開關（如 MOSFET、IGBT）的選型與應用風險管理。 3.熟悉 CAN、UART、SPI、I2C 等通訊協定及相關開發工具（如 STM32CubeIDE、MATLAB/Simulink）。 4.具備電磁干擾分析(EMI)及電磁相容性(EMC)設計與測試經驗 5.跨部門協作與溝通- ①與企劃、研發及生產團隊緊密合作，進行產品設計、驗證與量產導入 ②進行技術評審與決策，並向高層管理團隊匯報技術進展與風險評估 ✔學歷與經驗： ①電機工程、自動化控制、電子工程或相關領域本科以上學歷，碩士以上尤佳 ②至少 5年以上馬達驅動器或電機控制系統開發經驗，其中 2年以上團隊管理或專案領 導經驗 ✔分析與測試能力： ①熟練使用示波器、功率分析儀等測試工具進行調試與性能驗證 ②具備故障排除邏輯手法的引導與系統穩定性分析經驗 ✔產品研發與技術面管理： ①工作任務指派與協調、技職教育訓練擬定及執行 ②規劃與推動電控產品的技術路線和開發進度，確保項目如質如期。 ③管理產品開發過程中的風險與挑戰，並制定有效的技術解決方案 ✔加分條件： ①具備高速電機（如無人機電機、伺服電機）控制經驗者優先考慮 ②熟悉功能安全標準（如 IEC 61508、IEC62061）者尤佳

工作內容: 1.保健市場情報掌握及分析 2.商品開發及活動規劃 3.銷售分析及跨部門協調溝通 4.廠商維護及資源洽談 5.集團專案規畫及主管交辦事項

QE team expand in 2023! We‘re lookng for the experienced partner working together! Job Overview The Quality Engineer is responsible for supporting new product development, process development and product care through the application of Quality engineering skills for medical devices. This person will handle projects and tasks, from product/process inception through product launch, scale-up and maintenance and play an active role in the processes to ensure products meet quality standards consistent with Customer Requirement, while meeting all design control and other regulatory requirements, including, but not limited to FDA Quality System Regulation 21 CFR Part 820, ISO 13485, ISO 11608 & ISO 14971 Main Responsibilities • Team member representing Quality on new product/process development and product care projects. • Ensures that all design control and production / process control projects meet applicable regulatory (local and international), Corporate, Customer, and Local QMS requirements. • Assess and approve the risk mitigation techniques implemented and whether these are consistent with the product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls – UFMEA, DFMEA, PFMEA. • Develop quality plans and work further with Manufacturing on the transfer of quality requirements. • Promotes the use of statistics in the testing and control of quality. • Supports Device product/process development and production activities, including the following: - Develops or reviews product/process verifications/validation or test plans (protocols and reports). - Develops or reviews product/process specifications and requirements. - Develops or reviews product reliability specifications/predictions, reliability test activities. - Participates in risk management activities including review failure mode effects analysis (FMEA), hazard analysis, - fault tree analysis (FTA) and/or risk or statistical analysis. - Participates in product or process design and change activities, including design reviews. - Provides technical support for product quality attributes/decisions. - Support selected verification/validation activities (e.g., toxicology/biocompatibility, sterilization validation, etc.)with external suppliers. • Contributes to compilation and maintenance of Design History Files (DHF). • Ensures proper design and development documentation as per ISO 13485/FDA QSR Quality System Required Skills & Qualifications • Education:Technical / scientific degree at college / university level (mechanical, industrial, biomedical, chemical engineering, material/life science) Experience_Occupational experience • At least five years’ work experience in a Product Development/Design Assurance function in regulated environment (medical devices/Diagnostic instrumentation industry, pharmaceutical or biotechnology industry.) • Experience in the design and development of products in accordance with ISO 13485 guidelines. • In depth know-how and experience of quality techniques: Six Sigma Blackbelt, Six Sigma methods such as DFSS, DMAIC, DoE, FMEA, etc. • Experience in modular automation/fully automated assembly processes, particularly those involving plastic injection molded parts, mechanical spring, with integrated/non-integrated testings • Experience in the entire Design life-cycle and Phase-Gate development process. Experience_Special knowledge, expertise, experience • cGxP Know-How incl. regulations ISO 13485, FDA 21 CFR 820, MDD 93/42/EEC • Statistical methods • SAP (Manufacturing Execution Systems / MES will be an advantage) • English (spoken and written), local language (Mandarin) is a plus

1. 聯繫及拜訪產品供應商及客戶。 2. 既有產品及客戶開發維護。 3. 聯絡廠商及其它相關事務(如:報價、出貨安排、銷售、帳款回收…等) 4. 主管交辦事項(非經常性職責) 🔹🔹本職缺之聘僱職稱及薪資，仍依個人學經歷及內部職等核敘🔹🔹 🔹🔹除月薪外，另享有年終獎金、業績獎金…等變動性薪酬🔹🔹

🚀 加入禾秝安全系統工程有限公司 「你的技術，將成為守護安全的力量！」 ––––––––––––- 🔖【工作內容】 ▸安裝、維修監視系統與警報系統 ▸需懂 PC / 網路、電工基礎 ▸外出施工為主，需具備 汽機車 駕照 ––––––––––- ⏰【工作時間】 ✦日班 08:30–17:30（午休1小時） ✦週休二日 –––––––––––– 💰【薪資待遇】 • 面議 • 有工安證照者 ➝ 薪資加給 ––––––––––––- 🎁【福利制度】 ▶勞保、健保、員工團保 ▶員工生日禮金 ▶穩定工時、固定休假 ––––––––––- ✅ 條件需求 ☑ 學歷：高中職以上，不限科系 ☑ 經驗：有一年以上相關工作經驗尤佳 ☑ 駕照：自排小型車 / 普通重機車 ––––––––––––––- 📞【應徵方式】 請先利用 1111人力銀行 E-MAIL 履歷 或來電洽詢：何先生 (02)2600-8085 親洽面試請攜帶履歷（廣告商勿擾） 可面試日：週一～週五

1. Project Management and NPI Implementation: Oversee project scheduling and progress control, supporting the successful implementation of NPI to ensure on-time product launch. 2. RFQ Review and Quotation: Responsible for evaluating customer RFQs, preparing proposals and providing accurate quotations. 3. BOM Cost Management : Managing and maintaining BOM costs to ensure cost-effectiveness and alignment with market needs. 4. Cross-Functional Communication and Coordination: Collaborate with R&D, procurement, manufacturing, sales, and other departments to ensure smooth project execution and goal achievement. ＊彈性工作時間，薪優福利佳，並備有新店/中和線交通車＊

1.制定並推動AI技術在銀行業務中的應用策略，並進行治理管理 2.金融業新型態技術應用策略、推廣及追蹤 3.推動金融科技確保業務符合可持續發展目標