台大就業專區

1.介紹及銷售門市商品。 2.提供顧客之接待與需求服務 4.商品進貨入庫上架及下架 5.商品促銷陳列.檔期換檔 6.維護店櫃週遭之整潔 7.提供產品售後服務 薪資福利~ 1.業績目標達成獎金.團隊獎金.年終獎金.分紅獎金~挑戰年收入50-70萬 2.底薪31.7k+高額月獎金1-3萬 3.員工購機優惠 4.不定期聚餐 5.國內外員工旅遊 6.商品銷售獎金 ◎ 歡迎喜歡與人接觸、活潑及想挑戰高獎金的夥伴加入我們的行列

底薪31.7k，獎金制度透明，月平均挑戰收入45k 完整教育訓練，讓你能輕鬆上手。 及銷售服務等培訓計畫，提供線上教學資源 能在銷售領域脫穎而出。 工作內容 1.協助客戶手機簡易障礙排除 2. 電信門市服務與銷售 3.店務管理 4.庫存管理 薪資福利~ 1.業績目標達成獎金.團隊獎金.年終獎金.分紅獎金~挑戰年收入50-70萬 2.底薪31.7k+高額月獎金1-3萬 3.員工購機優惠 4.不定期聚餐 5.國內外員工旅遊 6.商品銷售獎金 7.月休10天(含國定假日).彈性排休

1.介紹及銷售門市商品。 2.提供顧客之接待與需求服務 4.商品進貨入庫上架及下架 5.商品促銷陳列.檔期換檔 6.維護店櫃週遭之整潔 7.提供產品售後服務 薪資福利~ 1.業績目標達成獎金.團隊獎金.年終獎金.分紅獎金~挑戰年收入50-70萬 2.底薪31.7k+高額月獎金1-3萬 3.月休10天(含國定假日).彈性排休 4.員工購機優惠 5.不定期聚餐 6.國內外員工旅遊 7.商品銷售獎金

登記資料、開發票、寄信、跑銀行、整理工廠、簡單管理、擅長使用EXCEL 需要會使用google 雲端資料庫 竤瑞機電工程有限公司 歡迎您與我們一起打拼。

本公司主要為生產泵浦(抽水機)，其工作項目為製造、維修、測試產品 1.泵浦(抽水機)現場組裝、吊拆。 2.泵浦(抽水機)檢修、維修。 3.需配合加班。 4.配合出差作業，依工作需求中北東部施工。不定期、需外宿。 5.配合上級指派任務。 6.無基礎有心學習者優。 7.配合公司派訓。

1.協助決策層制定發展策略。 2.統籌各部門共同制定出營運計畫。 3.協調推動各部門的工作朝著公司計畫的營運目標邁進，確保公司穩定成長。 4.推動各項改善專案的執行與落地。 5.推動並審核公司制度與流程的完善。 6.對公司各部門與主管進行指導與管理。 7.會網路行銷，業務管理，企劃能力

1.設備機械、機構、零組件之設計相關經驗 2.熟CAD SolidWorks繪圖軟體 3.主管交辦事項

1.負責業務開發及既有客戶服務 2.英文書信及國際貿易進出口貨品 3.懂網路行銷,做市場調查,海外通路延伸 4.處理主管交辦事宜及一般文書資料處理工作work,excel,... 5.偶有短期國內外出差 6. TOEIC多益 700 以上尤佳

1.提供嬰幼兒日常生活照顧。 2.安排適合嬰幼兒身心發展的各種學習活動。 3.培養幼兒學習自理生活。 4.教室教材管理及維護。 5.嬰幼兒每日生理、飲食等狀況記錄。 6.每日餐點採購烹煮。 7.廚房環境餐具用品管理。 8.每日清潔消毒及紀錄。

會計助理Accounting Assistant 📋【主要工作內容】 1.每月應收應付帳務處理及報表整理 2.發票開立、對帳與報稅作業 3.銀行帳戶、現金收支與零用金管理 4.協助編製各項財務報表及憑證整理 5.協助年度結帳、查帳及稅務申報 📍【工作地點】台中市(與面試地點相同) 🕰【工作時間】週一至週五 09:00–18:00，週休二日（需配合月結或稽核作業時可能延時） 📑【職務條件】 1.商學、會計、財務或相關科系畢業 2.熟悉 Excel、Word 3.具備一年以上會計相關工作經驗（或優秀應屆畢業生） 4.細心、負責，具備良好時間管理與溝通能力 💰【薪資制度與發展】 • 起薪範圍：NT$32,000起 • 試用期後考核調薪：依據任務完成度與協作能力進行調整 • 每季績效評估制度，優秀者享有專案獎金與升等機會 ※ 實際薪資依個人經歷、能力與證照狀況評估，可於面談時另議 【薪資調整】依照能力表現及各公司部門主管考核規範為主

一、學生諮詢與輔導 二、課程規劃與教學管理 三、招生與行銷推廣 四、行政與後勤協調 五、專業知識與進修 若有飛行經驗（如 CPL、ATPL、航校背景）或航空業經驗會大大加分。 疫情後 航空業大爆發~ 飛機維修/空服/地勤就業服務! 如果您對航空服務業有熱情! 如果您認為您值得接受培訓, 挑戰高薪! 歡迎加入我們的行列!

誠徵正職人員、儲備幹部 工作時間正職人員：5:00～13:00（假日13:30） 月休八天 工作內容： 1、櫃檯收銀、客席區清潔維護、茶品調製、 2、內場餐點製作、出餐、清潔、保養 3、沙拉製作、煮茶、食材分裝備料、環境清理 4、負責商品進貨入庫、銷售管理及庫存管理 能長期配合，有餐飲相關經驗者佳 樂於學習，願意接受培訓 喜歡與人互動，具備良好服務態度 喜歡早睡早起的夥伴

1.執行公司主管交辦的事務。 2.協助主管計劃和指揮人員相關的訓練及績效的評估。 3.案場接點、退場裝備準備。 4.人員排班、調度、督勤、代班、臨時性勤務支援。 5..社區(廠辦)會議(活動)召開支援。

1.執行管委會之決議 2.聘僱與解聘所屬員工 3.指揮監督所屬員工推行會務與業務 4.訓練、考核、獎懲所屬員工 5.社區行政文書處理 6.社區財務(管理費、零用金)... 等管理 7.社區修繕、維護..等發包工程業務 8.研擬及規劃社區短、中、長期管理、維護計畫 9.落實執行社區規約及管理辦法 10.執行區分所有權人大會決議事項

1.一般文書資料處理工作、簽核文件整理及發送，並負責追蹤執行狀況 2.安排賓客招待等事宜 3.定期記錄並核對總分類帳 4.應收/付帳款作業及零用金、管理費管理

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

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

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***

1.廠區清潔維護、備品補充。 　　 2.清潔機具設備操作。 3.依據公司管理系統、規範、班表，執行清潔作業。 4.VIP室暨公寓清潔維護。 5.其他主管交待工作事項。 6.須配合，隔周六加班