- 月薪40000元 台中市南屯區 2年工作經驗 1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 1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 1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 - 月薪40000~45000元 台北市信義區 工作經歷不拘 7天前更新展開
【薪 資】 無經驗起：本薪33500元+地區津貼3000元+地區津貼3500元=40000元★ 獎金另計，最高可達45000元。 以上薪資不含加班費。加班費另計。 【其他獎金】 業務獎金：一項可獲得2500~3000元。 導師獎金：一次可獲得2000元 循序漸進學習技能業務，教學相長，讓自己和團隊有成就感！ 【工作內容】 接待及引導、餐點介紹、協助顧客點餐、桌邊服務及維護環境等。 擺盤傳菜、食材準備、食材調理、廚房清理及維護環境等。 依照學習狀況習得技能加薪 【工作需求】 班別分為：早、中、晚班 每週排休兩天，每週排班，國定假日可再額外排休 【福利】 三節獎金、勞健保、每年健檢健康諮詢、員工折扣、員工餐、不定期部門聚餐等。
員工（調職）搬家安家費房屋（租賃）補助禮品三節獎金年終獎金 - 月薪55000~85000元 台中市北屯區 工作經歷不拘 2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 2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 2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 2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） 台北市松山區 5年工作經驗 今天剛更新展開
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 2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 2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 2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.
- 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 1天前更新展開
1.產業店舖市場的商圈調查。 2.預定點的開發及呈報核決。 3.茲約的議約、公正、用印。 4.年度降租規劃及執行。 5.工程及加盟業務的支援協調配合。 6.負責業務工作範圍：中/南區。
產假產檢假安胎假家庭照顧假員工生日禮金 - 面議（經常性薪資達4萬元或以上） 南投縣南投市 3年工作經驗 2天前更新展開
1. Per Each planning cycle to organize monthly sales forecast into campaign demand plan/bulk plan for production planning team to calculate the capacity requirement, material procurement plan and form the master schedule. 2. Prepare required data, challenge, reviews to report in monthly Domestic/Export S&OP meeting; confirming market demand with CS and Marketing team in the meeting. 3. Track demand forecast and sales/B2B order progress to ensure the supply schedule meets customer requirement. 4. Track production, testing and release progress to ensure the shipment schedule is followed. 5. New product launches-Ensure that all activities are aligned and provide timely submission of net requirements and orders. 6. Trigger escalation process as necessary. Identify and address potential supply issues pro-actively. Inform sales & marketing team on the potential supply risk timely. Recording all delay root cause for each shipment. 7. As Supply planner coordinate with demand planner, who oversees domestic market product, to manage local CMO PO Placement to meet inventory requirement. SPOC, escalation to TPP representatives for domestic TW CMO. 8. Intradepartmental communication and coordination and assisting in completing work assigned by superior.
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