-
職缺名稱公司名稱上班地點工作經驗更新薪資待遇
- 面議（經常性薪資達4萬元或以上） 台南市安平區 3年工作經驗 1天前更新展開
1. 負責部門行政制度建立，工作流程規劃，改善提高工作效能。 2. 協助部門處理案件之執行、管理、問題追蹤及解決。 3. 處理公文及審閱會簽相關文件。 4. 進行公部門工作業務協調溝通。 5. 須有太陽光電送件經驗。
產假產檢假安胎假家庭照顧假年節獎金 - 月薪40000元 台中市南屯區 2年工作經驗 3天前更新展開
以灶腳為舞台，台灣四季特色食材為主角， 傳承三代的精湛手藝，蘊藏媽媽的細膩用心，呈現台菜醇厚與鮮爽並存的好滋味。 饗要加入真珠的你，無經驗沒關係，我們手把手的帶你，只要你願意接受公司培訓，喜歡接觸人群，在乎人與人之間的互動，熱愛台式料理，有熱忱的心態，想要在餐飲業中闖蕩，饗賓給你發揮的舞台！ 【學習目標】 1.執行桌邊及餐食服務，如倒水、點菜、送菜、控菜、撤桌等工作 2.負責開餐前準備工作，補齊工作站內之餐具及備品 3.維持負責區域之整潔，以提供顧客舒適乾淨的用餐環境 4.負責營業結束後工作站之清潔及各項善後工作 ※請先投遞履歷，之後將有專人與您聯繫，安排面試時間、地點。 *******饗賓餐旅集團誠摯邀請您的加入，成為最受期待的餐飲集團******* Facebook饗賓招募粉絲頁：https://www.facebook.com/eatogether.hr/
產假產檢假年終獎金三節獎金績效獎金 - 月薪46200元 台中市南屯區 5年工作經驗 3天前更新展開
以灶腳為舞台，台灣四季特色食材為主角， 傳承三代的精湛手藝，蘊藏媽媽的細膩用心，呈現台菜醇厚與鮮爽並存的好滋味。 饗要加入真珠的你，無經驗沒關係，我們手把手的帶你，只要你願意接受公司培訓，喜歡接觸人群，在乎人與人之間的互動，熱愛台式料理，有熱忱的心態，想要在餐飲業中闖蕩，饗賓給你發揮的舞台！ 【學習目標】 1.落實現場各站別工作準則 2.執行教育訓練基層人員 3.安排現場人力調度 4.協助顧客抱怨處理 5.負責領貨、進貨及物料盤點 ※請先投遞履歷，之後將有專人與您聯繫，安排面試時間、地點。 *******饗賓餐旅集團誠摯邀請您的加入，成為最受期待的餐飲集團******* Facebook饗賓招募粉絲頁：https://www.facebook.com/eatogether.hr/
產假產檢假年終獎金三節獎金績效獎金 - 面議（經常性薪資達4萬元或以上） 台北市大安區 2年工作經驗 3天前更新展開
【工作內容】 1.展店規劃建置與執行 (工程進度掌控、成本預算控制、工務協調) 。 2.專案分析及工程研發 3.工程技術評估及建築法令評估 4.餐廳設計管理 5.規劃、監督、管理與開發工程與維護相關廠商。 粉絲頁按讚追蹤饗賓即時訊息： Facebook饗賓招募粉絲頁：https://www.facebook.com/eatogether.hr/ *******饗賓餐飲集團誠摯邀請您的加入，成為最受期待的餐飲集團*******
產假產檢假年終獎金三節獎金績效獎金 - 面議（經常性薪資達4萬元或以上） 台南市安平區 3年工作經驗 4天前更新展開
1. 太陽能系統工程管理(物料掌控、進度掌控、品質時程控管)。 2. 包商溝通、協商管理、合約規範訂定以及施工前會議。 3. 工程成本估價、新物料、規範、工法評估。 4. 有太陽光電產業相關經驗尤佳。 5. 可帶領監造工程師團隊執行公司目標。
產假產檢假安胎假家庭照顧假年節獎金 - 面議（經常性薪資達4萬元或以上） 高雄市前金區 2年工作經驗 2天前更新展開
1.需求分析：了解客戶的需求和喜好，制定設計目標。 2.空間規劃：根據功能需求，進行空間布局和規劃。 3.設計概念：創造整體設計風格和主題，包括顏色、材質和家具選擇。 4.繪製設計圖：製作平面圖、立面圖和3D模型，展示設計方案。 5.材料選擇：選擇合適的建材和裝飾材料，考慮實用性與美觀性。 6.預算管理：估算設計項目的成本，協助客戶控制預算。 7.監工和協調：與施工隊伍、供應商和其他專業人員協作，確保設計按計劃實施。 8.客戶溝通：與客戶保持良好溝通，隨時調整設計以滿足需求。
年終獎金伙食津貼員工聚餐尾牙員工國內、外進修補助 - 月薪55000~85000元 台中市北屯區 工作經歷不拘 4天前更新展開
1. 以Revit建置建築、結構及機電模型，檢討碰撞及修改，提出釋疑予設計單位回覆，產出2D施工圖並回饋施工現場。 2. 進駐工務所繪製施工圖，完成2D施工圖送審及竣工圖繪製。 3. 主管交辦事項執行及BIM相關創新應用（如數量計算、4D工序模擬） 4. 熟營建工程施工圖彙整及問題檢討，提供3D圖說，並參與相關會議討論及記錄議題，追蹤議題完成解決。
全勤獎金年終獎金三節獎金績效獎金員工團保 - 面議（經常性薪資達4萬元或以上） 台北市信義區 2年工作經驗 31天前更新展開
1. Evaluation of submission feasibility for in-licensed products (major) and domestically manufactured products in the APAC region (KR, TW, HK, SG, MY, TH, VN, PH, and ID) 2. Coordination of the due diligence and production of the gap list 3. Evaluation and plan of the design, the budget, and the timeline for the bioequivalence study, the bridging study, and the clinical study in KR and TW 4. Communication with the APAC regulatory teams and partner companies to resolve the submission gap in the target markets 5. Design and consolidation of the regulatory strategy of the key milestone, the submission pathway, the submission timeline, and the launch timeline in the target markets 6. To review the License and Service Agreement 7. To support new submissions in Taiwan 8. To update of the APAC regulations 9. To prepare the consultation materials 10.To provide the justification materials on the non-clinical and clinical studies for the deficiency letter 11. To compile the ACTD format from the CTD format 12. To monitor submission progress on all company‘s projects 13. To provide improvement plans 14. The other tasks 1. 協調法規相關部門與供應商評價授權產品 2. 評估產品於亞太地區註冊之可行性，準備註冊所需相關技術文件與試驗 3. 在產品開發及送件準備期間提供法規要求的指引，協助其符合國際法規 4. 即時提供註冊用產品主檔案 5. 協助提供法規更新計畫 6. 即時支援產品維護用技術文件 7. 協助擬定合理且經濟可行之註冊計畫 8. 協助執行註冊計畫
- 面議（經常性薪資達4萬元或以上） 台北市信義區 3年工作經驗 31天前更新展開
1. Plan and execute internal audits and special projects to evaluate the risks and the effectiveness of related controls. 2. Prepare reports for each engagement and communicate audit observations with corporate, regional, and local management. Apply problem solving skills to issues and provide practical and constructive recommendations. 3. Develop credibility and trust with operating functions to value-add internal controls and management. 4. Monitor changes in Company policies and procedures to align with the applicable Regulations, Standards, and industry practices.
- 面議（經常性薪資達4萬元或以上） 台北市信義區 6年工作經驗 31天前更新展開
1. Support and facilitate business user‘s requirement to seamlessly running at corporate SAP system in the landscape via analyzing, designing, and developing. 2. Work closely with the team (other SAP developers, infrastructure & system teammates) to understand business needs and deliver features in good quality at timely manner. 3. Be capable of creating and assessing software architecture/designs with multiple stakeholders. 4. Manage overall change request and/or incident backlog for the owned topics and ensure the high quality of corrections and notes for the owned topic areas and of stable assist packages with no regressions. 5. Exhibit learning agility by quickly upskilling on new tasks and concepts. 6. Assist our business users during product deployment, critical operations, and system rollout via standard infrastructure, creating maintenance notes and documentation. 7. Will be providing presentations and workshops.
- 面議（經常性薪資達4萬元或以上） 台北市大安區 5年工作經驗 2天前更新展開
1.大型(複合型)專案規畫設計。 2 協助產品定位、圖說審核、施工界面了解與執行。 3.行政審查及專案預算控管。 4.主管交辦事項
員工國內、外進修補助員工及眷屬喪葬補助員工購物優惠國內、外旅遊補助社團補助 - 面議（經常性薪資達4萬元或以上） 南投縣南投市 1年工作經驗 31天前更新展開
1.開發調整分析方法(HPLC, GC, IC...)，協助產品製程開發，分析方法之確校 2.執行實驗室設備3Q 3.研擬審查藥典相關產品規格及分析測試，建立藥典規格 4.操作化學分析儀器進行分析，協助產品放行
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 5年工作經驗 31天前更新展開
1. Review and provide the technical recommendations for CMC documentation and Common Technical Document(CTD) dossier from a regulatory perspective. 2. Interpretation and Handling the regulatory technical query’s responses that were asked by Client and Authority during the due diligence or submission deficiency phase and provide the action plan or solution and scientific justification. 3. Responsible for evaluating the registration feasibility and mapping the global registration strategy for assigned new R&D products. 4. Cooperate and teamwork with R&D, technical, and RA PM on new R&D project technical challenges and complete the dossier till product approval. 5. Responsible for regulatory registration for export products and make sure all the documents are meet the authority‘s requirements. 6. Responsible for deficiency response preparation to ensure our response meets the authority’s requirements. 7. Accurately follow the update of the registration regulation, and provide the regulation update to the team and training.
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 10年工作經驗 31天前更新展開
OVERALL OBJECTIVES: -Provide leadership and oversight of designated GxP Computerized Systems (that have are relevant for Lotus Pharmaceutical) and their support teams to ensure successful delivery of key objectives, as well as compliance with applicable business and regulatory requirements. -Work with teams to implement quality systems and improvements that meet local business and regulatory requirements. -Responsibilities include administration and management of the Electronic Document Management System (EDMS), Electronic Quality Management System (EQMS), Learning Management System (LMS), as well as extended support and oversight of other GxP systems. GENERAL DUTIES: -Ensure the following key areas of GxP computerized system governance are established and maintained for applicable systems -Management: Validation planning, supplier assessment, risk management -Development 1. Validation approach & deliverables – maintain current “as is” validation state 2. Configuration and design 3. Management, development, testing, and review of software 4. Data management -Operation 1. Support services, performance monitoring, incident management, security, training, user authorizations 2. CAPA, change management, updates/patches, repair activity 3. Data integrity, periodic review, backup and restore, business continuity -Quality lead on designated Computer Systems implementations, ensuring all regulatory and compliance issues are addressed and documented -Mentor staff working on GxP computer system validation -Lead and support improvement projects to solve problems, enhance system capabilities, and expand use of GxP systems to new sites and functional areas in need. -Work with relevant teams to maintain capabilities for collecting and reporting Quality data and projects, including maintaining Quality SharePoint Portals where necessary. -Participate in internal and supplier audits as requested. -Participate in improvement initiatives and programs as requested. -Stay current with GxP and industry standards QUALIFICATIONS: -Bachelor’s degree in pharmacy or life science, or higher degree, with the right combination of extensive experience and success in the pharmaceutical industry -Education in computer science, coding or programming is a benefit -Thorough knowledge of pharmaceutical industry, quality systems, computerized system validation, GAMP 5, and relevant GxP and data integrity requirements. -Experience and skills related to the operation, administration, and overall governance of GxP computer systems and software applications. -Working knowledge of help desk software/support, databases, SaaS, and analytical reporting -Strong technical background and ability to explain complex information in simple, clear terms to non-IT personnel. Ability to assess customers IT knowledge and provide appropriate support. -Proven track record of successful GxP Computer System implementations and governance. -More than 10 years’ experience in different quality related roles within the pharmaceutical industry -Good knowledge and experience in Project Management principles and techniques. -Thorough knowledge of Quality Systems and risk-based decision making. -Experience dealing directly with regulatory agencies -Experience and skills in operating across and between different national cultures. -Good command of Mandarin and English SKILLS: -Strong leadership/team management skills -Credible and confident communicator with good presentation skills (written and verbal). -Strategic thinker with the ability to influence at all levels -Strong analytical and problem-solving ability, including identifying potential solutions, recommending and implementing methods, procedures and/or techniques for resolution. -Able to work proactively and independently.
-
上一頁 下一頁
第 2711 / 4237 頁
第 2701 / 4237 頁第 2702 / 4237 頁第 2703 / 4237 頁第 2704 / 4237 頁第 2705 / 4237 頁第 2706 / 4237 頁第 2707 / 4237 頁第 2708 / 4237 頁第 2709 / 4237 頁第 2710 / 4237 頁第 2711 / 4237 頁第 2712 / 4237 頁第 2713 / 4237 頁第 2714 / 4237 頁第 2715 / 4237 頁第 2716 / 4237 頁第 2717 / 4237 頁第 2718 / 4237 頁第 2719 / 4237 頁第 2720 / 4237 頁第 2721 / 4237 頁
