桃園市轉職工作機會，轉職跳槽推薦工作，提供履歷健診等強化服務|1111轉職專區-第419頁

(固定休六日)CNC銑床專員初階人員起薪4.2萬中階人員4.8萬高階人員5.5萬
企業名宇盟實業有限公司
工作地點桃園市龜山區
薪資月薪42000~55000元
工作內容使用面板操作CNC，初階人員能獨立作業後，起薪42000 初階人員起薪4.2萬中階人員4.8萬高階人員5.5萬

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

(桃)中壢校-兒童數學老師
企業名奧林匹克文化事業股份有限公司
工作地點桃園市中壢區
薪資月薪28590~35000元
工作內容 🌟【兒童數學老師】讓孩子從小愛上數學的第一步，就由你帶領！你相信數學不只是考試科目，而是一種好玩的思考遊戲嗎？你願意陪著孩子從0開始，一步一步建立邏輯與自信嗎？如果你喜歡孩子、喜歡數學、喜歡教學，那你就是我們要找的人！ 🔹我們是誰？「奧林匹克資優數學兒童才藝班」是專為幼兒園與低年級國小生設計的邏輯思維養成課程，透過教具、遊戲、故事與圖像式學習，將數學轉化成孩子最喜歡的活動！目前班型以一對一／小型團班為主，注重教學互動與個別差異引導。 🔍【我們正在找的你】 👩‍🏫 喜歡與孩子相處，願意蹲下來用孩子的語言溝通 🧮 對數學、邏輯、推理有基本理解（具備國小數學程度即可） 💗 有耐心、有責任感，願意陪孩子成長、願意自我學習 📚 想在教育領域累積經驗，歡迎新鮮人加入我們團隊！ ✨【你會做什麼】引導幼兒進行教具操作與邏輯推理遊戲教授基礎數概念：分類、對應、順序、加減邏輯、圖形認知等發展孩子的思考力、自信心、觀察力與專注力與家長簡單回饋孩子上課狀況定期接受在職培訓，逐步進階為「奧數專業師資」 🛠【我們提供的支持與養成制度】 🔸 完整職前培訓，即使你沒有教學經驗也不用怕 🔸 每月定期教學研討與進修計畫，幫你快速成長 🔸 提供教材、教具與課綱設計，備課專業不馬虎 🔸 優秀教師有機會晉升課程講師／教學主管／訓練講師等職務 🔸 穩定周休二日制度，讓你兼顧生活與工作 🎯【我們的理念】我們相信：孩子的數學能力不是靠背誦練出來，而是從「玩」中養成，從「探索」中建立邏輯，從「鼓勵」中培養自信。我們希望未來的老師們，不只是傳授知識，而是啟發思維、創造連結、給孩子成長的勇氣。 📢 不管你是教育相關科系的新鮮人或者是想找一份有意義、有溫度的長期工作 👉 現在就是你展開教育旅程的時候！加入我們，一起打造孩子數學起步最重要的起點💡

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

採購人員(鄰近好市多) 面試心得
企業名日禕紡織企業股份有限公司
工作地點桃園市觀音區
薪資月薪30000~40000元
工作內容 1. 根據原料的庫存量，執行訂購作業。 2. 處理貨品遺失或延遲的採購問題。 3. 採購單回簽、紗廠TC申請作業。 4. 建立、更新供應商資料（如：貨品價格、規格和到貨時間），以選擇最佳供應商。 5. 負責協助商品採購及採購開發工作。 6. 協助採購單的查詢及下單的工作。 7. 追蹤樣品郵寄。(異常原料胚布分析) 8. 與工廠安排進貨日期。 9. 處理原料異常的客訴。 10. 建立優良供應商評鑑程序。 11. 建立原物料和設備之報廢或折讓處理程序。

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

MFMC - 金屬量產技術師
企業名瑞健股份有限公司
工作地點桃園市蘆竹區
薪資月薪35000~0元
工作內容工作內容- 01. 操作與維護生產設備，並確保其功能能夠正常生產 02. 負責並參與設備、生產技術及流程改善 03. 主管交辦事項

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

MFMP - 組裝技術師 (六福廠)
企業名瑞健股份有限公司
工作地點桃園市蘆竹區
薪資月薪35000~0元
工作內容請直接透過我們的公司網站提交您的申請： https://careers.shl-medical.com/job/MFMP-％E7％B5％84％E8％A3％9D％E6％8A％80％E8％A1％93％E5％B8％AB/571-zh_TW/ 【關於瑞健】瑞健醫療 ( SHL Medical ) 為領航全球的藥物輸送解決方案供應商，在設計、研發及製造先進藥物輸送系統上居龍頭地位，產品含括自動注射器、筆型注射器與穿戴式藥物輸送系統等。【職缺簡介】 MFMP的生產模式為自動化組裝，主要將前段的塑件及鐵件進行自動化的組裝，組裝的成品可區分為上本體、下本體【工作內容】 • 設備巡檢、保養、異常排除、故障檢修及品質確認 • 監控產線整體設備效率(OEE)、產出、不良率與參數設定 • 主導產線機台每日點檢項目 • 參與機台與製程提升與改善活動 • 完成主管交辦有關生產產品、程序事宜 ***薪資未含輪班津貼、加班費與獎金***

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

RAD_Risk Analysis Engineer
企業名瑞健股份有限公司
工作地點桃園市蘆竹區
薪資月薪35000~0元
工作內容 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, SHL has sites in Sweden, Taiwan, and the Unites States. Job Overview The role requires application of engineering knowledge and ingenuity to deliver risk analysis related to medical device manufacturing processes using tools such as - Failure Mode and Effect Analysis (FMEA). The candidate will work with cross-functional teams to ensure processes development, control planning and qualification of manufacturing processes are aligned with risk-based approach and meets ISO 14971:2019 requirements. Main Responsibilities • Develop Assembly Risk Assessment document from Assembly Guidance of product to ensure control plan and process development are done according to product risk levels • Participate in process and equipment design review activities and conduct comprehensive Failure Mode and Effect Analysis (FMEA) of manufacturing processes and related equipment to ensure risk exposure to product and end used is reduced as far as possible at design stage. • Attend relevant project meetings to ensure all information required to develop, update, and maintain risk management documents for related projects are captured and utilized effectively. • Participate in relevant product lifecycle management activities to provide/collect information and ensure FMEAs are updated accordingly – e.g., NCMR & complaints, CCB meetings, MPQ meetings, deviations meeting etc. • Ensure periodic review and update of FMEAs according to comply with procedural and compliance requirements. • Cascade information and actively participate to propose risk control methods in control planning, process development and equipment development stages through use of ARA and FMEA. • Where needed, participate and contribute on end-to-end processes risk management in SHL including material handling, transportation, packaging, sterility and testing of final combination product. • Organize cross-functional meetings with project team members to communicate all open items from FMEA reports and derive solutions to mitigate the risks. This includes active engagement with AMSD and external equipment suppliers where needed. • Escalate potential issues and progress blockers on risk management work to team leaders and ensuring resolution is achieved with minimal impact to project timeline. Skills and Qualification •Masters in Life Science Engineering discipline (or) Degree with 2 years of work experience. Exposure to medical device, pharmaceutical or biotechnology industry is added advantage. • Trained on Quality System Regulation, Process Validation, Risk Management or Design Control course. • Demonstrated and applied a broad knowledge in quality management assignments and risk management approaches. • Good communication and interpersonal skills and demonstrate ability to participate in inter-departmental projects and resolve quality-related issues in a timely and effective manner. We Offer • An exciting opportunity in a fast-growing international medical device company • A modern working environment, with multicultural and dynamic teams • Flexible working hours and a hybrid remote work policy

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

QE - Senior Quality Engineer (Product Design/Process Design)
企業名瑞健股份有限公司
工作地點桃園市蘆竹區
薪資月薪35000~0元
工作內容 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

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

FCTY_警衛人員(自聘，8小時制，保障14個月)
企業名瑞健股份有限公司
工作地點桃園市蘆竹區
薪資月薪36000~0元
工作內容 01. 門禁管制及車輛進出指揮。 02. 訪客進出登記及換證。 03. 訪客拜訪通知相關單位及引導。 04. 注意公司門面確保乾淨整潔。 05. 廠區巡視維護廠區安全。 06. 夜間監看監視器畫面留意可疑及回報。 07. 確保廠區安全公共安全，避免火災、竊盜及其他危害。 08. 其他臨時主管交辦事項。

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

PDPE_Senior Project Engineer 資深專案工程師
企業名瑞健股份有限公司
工作地點桃園市蘆竹區
薪資月薪36000~0元
工作內容 SHL Medical is the world-leading solution provider in the design, development, and manufacturing of advanced drug delivery systems for the past 30 years 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 with sites in Sweden, Taiwan, and the Unites States. Job Overview This position is for a senior technical role in Project Engineering Dept. in Taiwan. You will lead and be accountable for the Engineering activities related to the development of medical drug delivery systems. Main Responsibilities - Lead and develop a technical team of experts to support the industrialization of our autoinjectors - Lead and manage the Subject Matter Experts (SME) from different fields related to tooling, injection molding, spring manufacturing, metal parts processing and assembly automation. - Understand current practices and develop new or improved processes and methodologies based on in-depth processing experience. - Promote use of new technologies and industry-leading trends. Provide the highest level of technical expertise. - Lead Root Cause Analysis (RCA) using problem-solving methods and tools. - Collaborate closely with plant/production manager, tool makers and maintenance, quality and process development on performance/process improvements and trouble shooting. - Lead the development of improvement plans and requirements for capacity expansion in collaboration with our Technology Transfer team. - Lead Design for Manufacturing & Assembly (DFMA) activities and define the manufacturing requirements for new products and product care initiatives. - Mentor our future generation of engineers and serve as a Subject Matter Expert (SME) in engineering. Skills and Qualification - Degree in Mechanical Engineering, Polymer Science or similar education/experience. - Minimum 6 years of relevant industry experience with hands-on experience with injection molding systems and/or automation equipment. - Deep understanding of medical device development operations, with experience in leading technical projects e.g., cost savings initiatives or new supplier introductions. - Statistical analysis knowledge, including an understanding of scientific molding processes, the mold- machine- material- process interactions, Design of Experiments (DoE) and mold qualification protocols - Advanced knowledge on problem-solving and Root Cause Analysis (RCA) methodologies, six sigma certification a plus. - Proven track record in leading and developing a team of highly specialized experts; management experience. - Advanced knowledge in process development, verification and validation. - Passionate & committed self-starter with an “own it” and “can do” attitude, team player and taking responsibility to get the job done. - Able to professionally communicate with stakeholders, upper management, and external parties. - Resilient and able to work under pressure. - Pragmatic and data-driven mind. - Previous exposure to a highly regulated industry (e.g. medical, pharmaceutical) and knowledge of relevant standards (e.g. ISO13485, cGMP) is a plus. - Intercultural and interdisciplinary communication skills; able to communicate effectively in English (verbal, written) (TOEIC 750 and above).

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

MFMG - 射出成型作業員（六福廠）
企業名瑞健股份有限公司
工作地點桃園市蘆竹區
薪資月薪29000~0元
工作內容【關於瑞健】瑞健醫療 ( SHL Medical ) 為領航全球的藥物輸送解決方案供應商，在設計、研發及製造先進藥物輸送系統上居龍頭地位，產品含括自動注射器、筆型注射器與穿戴式藥物輸送系統等。【工作內容】 • 進行製造現場的產品組裝、檢驗、包裝出貨等作業（大約5-10公斤） • 填寫生產報表，以檢視與生產目標的距離 • 完成主管交辦有關生產產品、程序事宜【人才需求】 • 12小時，4休3制（早班 0800-2000 / 夜班2000-0800） • 是生產狀況需配合加班 • 數字觀念清楚、細心度佳

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應徵

工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

10/31

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