- 月薪30000~40000元 高雄市鼓山區 2年工作經驗 1天前更新展開
1.醫療相關產品行銷推廣 : CT和植牙等等.. 2.開發及關係經營：拜訪固定或非固定公司客戶，進行名單開發及關係維護 3.售後服務之提供：協助客戶使用產品及問題諮詢，提供新通路商相關之行銷或經營輔導
績效獎金國內旅遊國外旅遊員工聚餐生育補助 - 月薪35000~50000元 新北市五股區 工作經歷不拘 4天前更新展開
1. Write, edit and review user manuals, quick guides, technical documents or sales kits of medical devices in English. 2. Technical documents writing including: - Risk management plan - Software validation plan - Performance summary report
產假產檢假年節獎金員工生日禮金年終獎金 - 月薪30000~42000元 高雄市路竹區 1年工作經驗 4天前更新展開
1.業務績效目標達成 2.顧客開發與客戶關係維繫 3.顧客連絡資料整理、出口資料製作 4.負責詢報價單文件之整理，建檔以及追蹤，於有效時間內回覆顧客信件 5.協助客戶對於商品價格的查詢及報價相關的問題 6.客訴處理、提高客戶滿意度 7.假日不定期國內外参展與準備 8.完成主管其他交辦事項 9.能獨立作業者為佳. ～～對加工流程略懂者尤佳～～
產假全勤獎金年終獎金員工團保員工公出特別保險 - 月薪30900~32000元 新北市五股區 1年工作經驗 2天前更新展開
1.生產設備之參數設定及維護 2.製程良率提升及不良原因分析 3.協助生產排程之執行與數據收集分析 4.設備保養計畫訂定與執行 5.其他主管交辦事項
產假產檢假年節獎金員工生日禮金年終獎金 - 月薪27470~32000元 新北市樹林區 工作經歷不拘 12天前更新展開
1.協助工程師執行產品量測、測試、驗證與量產導入 2.協助工程師執行生產或檢驗設備導入測試與驗證 3.協助工程師撰寫產品技術文件 4.偶爾需看英文規範文件
產假全勤獎金年終獎金員工公出特別保險誤餐費 - 月薪30000元 台中市烏日區 2年工作經驗 今天剛更新展開
歡迎加入宏瑋醫材、宏瑋寵物 寵愛自己更是寵愛毛孩子 1. 評估耗材物料安全庫存量，比價、議價後執行相關採購作業及交期追蹤。 2.ERP系統使用：基本資料維護/採購進退貨單輸入。 3.供應商管理及建立。 4.每月採購預成本估算及報表製作。 5.跟催採購物料需求與交期回覆等細節。 6.耗材管理。 7.其他主管交辦事項. *能配合公司遷至草屯廠*
員工在職教育訓練良好升遷制度產假全勤獎金年節獎金 - 月薪50000元 台北市大安區 工作經歷不拘 5天前更新展開
Job Description Provides highly visible customer support through the performance of on-site installation, as well as overseeing any necessary diagnoses, troubleshooting, service, and repair of complex equipment and systems. Checks out and approves operational quality of system equipment. Instructs customers in the operation and maintenance of the system. Serves as company liaison with customer on administrative and technical matters for assigned projects. Interprets customers’ needs and clarifies if the responsibility for problem resolution falls to sales personnel, customer support reps, or engineers. This job may include any aspect of field support, and is not limited to system hardware and software, PCs, and networking/wireless networking Installs and upgrades a wide range of complex and advanced company products according to technical documentation and company guidelines to ensure that customer’s equipment operates efficiently. Demonstrate to customer equipment operation and specification according to Customer Acceptance Procedure (CAP). Instruct customers in operation and basic maintenance of VMS products. Requires no direct supervision. May coordinate and review the activities of a small group of Installation Representatives. May coordinate other expert company resources required to assist in performing the installation or upgrade activities. Applicable to the Oncology Systems business only: Position must have full access to VMS client sites to perform the essential functions of this position. Many VMS clients require VMS employees and representatives to meet certain “Vendor Credentialing” requirements before they will be allowed to have access to their sites. Unless prohibited by law, position must meet all Vendor Credentialing requirements necessary to have full client access, and must continue to meet those requirements during the course of VMS employment in this position.
員工結婚補助尾牙員工聚餐國內旅遊員工停車位或停車補助 - 月薪28000元 桃園市蘆竹區 1年工作經驗 11天前更新展開
保障年薪14個月，到職即享有10天特休(年度在職比例給予天數) 上班時間: 7:00~16:00 無空班 1. 處理烹飪前與烹飪中之準備工作。 2. 廚房清潔工作。 3. 其它主管交辦事項。
產假員工停車位或停車補助員工餐廳按摩室國內旅遊 - 月薪35000元 桃園市蘆竹區 工作經歷不拘 11天前更新展開
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
產假員工停車位或停車補助員工餐廳按摩室國內旅遊 - 面議（經常性薪資達4萬元或以上） 桃園市蘆竹區 3年工作經驗 11天前更新展開
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
產假員工停車位或停車補助員工餐廳按摩室國內旅遊 - 面議（經常性薪資達4萬元或以上） 桃園市蘆竹區 5年工作經驗 11天前更新展開
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
產假員工停車位或停車補助員工餐廳按摩室國內旅遊 - 面議（經常性薪資達4萬元或以上） 桃園市蘆竹區 3年工作經驗 11天前更新展開
【關於瑞健】 瑞健股份有限公司(SHL Medical)為領航全球的藥物輸送解決方案供應商，最主要的產品為自動注射器及筆型注射器。台灣為瑞健最大的營運據點，共三個廠區坐落於桃園。瑞健提供客人一條龍式的服務，包含設計、研發、驗證、確校、量產及組裝，客戶來自全球排名前25的大藥廠。職缺簡介 【職缺簡介】 設備工程師/技術師將依據公司發展策略，針對生產設備維護保養計畫執行保養管制作業和設備異常狀態排除、異常分析與追蹤處理，以減少異常狀態發生頻率，並執行設備、生產及流程改善計畫，使改善計畫得順利完成，以提升設備生產效能並確保設備運作正常。 【工作職掌】 ●生產設備維修 ●生產設備定期保養 ●射出成形設備維修
產假員工停車位或停車補助員工餐廳按摩室國內旅遊 -
