- 月薪30000~40000元 高雄市鼓山區 1年工作經驗 今天剛更新展開
1. 負責倉處理商品出貨/進貨盤點/上架/理貨/測機/貼標等相關作業 2. 商品瑕疵檢查 / 短到彙報等 3. 商品包裝 / 出貨 / 郵局寄貨/ 聯絡貨運行等出貨相關作業 4. 配合業務需求/ 理貨 / 出貨等相關作業 5. 倉庫定期整理 / 維持工作區域環境整潔 / 產品依有效期限擺放整齊 6. 使用ERP系統，協助各項資訊之即時更新與維護。 7. 其它行政庶務及主管交辦事項 8. 做事細心有條理 / 具工作責任感 / 配合度佳 / 抗壓性高 / 字體端正
年終獎金三節獎金員工聚餐尾牙春酒 - 月薪30000元 台北市松山區 1年工作經驗 1天前更新展開
1.物料保存管理，確保品質 2.定期清點物料，並將物料標示並放於正確位置，必要對相關人員解說，使其容易使用 3.定期追蹤複查庫存與紀錄是否相輔有無損壞，如不符合找出原因 4.定期清潔庫存、工具、設備或貯藏室，以確保符合安全規章及存貨安全 5.倉庫物品、物料進出管理品，與請購單、發票及其他憑證是否相符 6.將進貨登入及存貨報表 7.貨品的輸送與成品包裝 8.物料倉儲的管理 9.有ERP的操作經驗
績效獎金國內旅遊國外旅遊員工聚餐生育補助 - 月薪37000~43000元 桃園市桃園區 工作經歷不拘 1天前更新展開
本公司為醫院藥局設備廠商,主要營業項目為大型全自動錠劑分包機,工程師主要工作是到各醫院從事分包機定期保養及維修,偶爾會有夜間或假日叫修,(工作待遇包含績效獎金)
產假產檢假員工生日禮金年終獎金三節獎金 - 月薪28590元 高雄市路竹區 工作經歷不拘 3天前更新展開
1.基本識圖。 2.尺寸量測。 3.部品上下料。 4.成品去毛邊 , 研磨拋光及機台生產基礎操作。 5.機台故障排除。 6.無經驗可。
產假全勤獎金年終獎金員工團保員工公出特別保險 - 月薪37000~43000元 台南市東區 工作經歷不拘 2天前更新展開
本公司為大型包藥機設備廠商,主要配合客戶作業時間，至客戶端進行定期檢查及保養,故障時緊急叫修處理。(偶有假日或夜間叫修)
產假產檢假員工生日禮金年終獎金三節獎金 - 月薪30000~42000元 高雄市路竹區 工作經歷不拘 2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. ～略懂加工流程者為佳～ ～具業績積極提升與業務開發態度者優先錄取～
產假全勤獎金年終獎金員工團保員工公出特別保險 - 月薪35000元 桃園市蘆竹區 工作經歷不拘 1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 - 月薪35000元 桃園市蘆竹區 工作經歷不拘 1天前更新展開
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***
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 1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 1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 - 月薪36000元 桃園市蘆竹區 1年工作經驗 1天前更新展開
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。
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 1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 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).
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29000元 桃園市蘆竹區 工作經歷不拘 1天前更新展開
【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
產假員工停車位或停車補助員工餐廳按摩室國內旅遊 -
