轉職找工作推薦

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工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • 內場廚房廚師。儲備幹部。學徒可
  • 企業名 法貝諾義式小館
  • 工作地點 台中市西屯區
  • 薪資 月薪40000~55000元
  • 工作內容 1. 負責洗、剝、削、切各種食材，以完成烹飪的前置工作。 2. 協助廚師測量食材的容量與重量。 3. 依照客人的點單，準備不同菜色所需要的食材。 4. 於出菜時負責菜餚擺盤或調整份量之工作。 5. 協助打包外帶的食物，必要時進行外送的服務。 6. 將洗好的餐盤收到儲藏櫃內，並在即將使用前預先加熱。 7. 負責前台與後台之訊息傳遞，隨時回報後台的出菜進度給餐廳經理。 8. 負責清理工作環境、設備及餐具。
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    • 法貝諾義式小館-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • 【國泰集團】健檢檢驗師(內湖)

    員工旅遊供餐福利年終獎金

  • 企業名 國泰健康管理顧問股份有限公司
  • 工作地點 台北市大安區
  • 薪資 月薪40000~48000元
  • 工作內容 ※工作內容 1.執行檢驗相關作業流程(例如：協助外送檢體分裝、檢驗室文件資料建檔、客戶條碼預簽、待驗檢體前處理、外送報告核對、檢驗科儀器品管校正、檢驗作業執行與報告核發) 2.迎賓時傾聽客戶需求，適時推廣檢驗相關項目，提升營收 3.配合實驗室認證各項事宜 4.客訴、異常或緊急事件通報與處理 5.其他主管交辦事項 ※月薪範圍：40,000~48,000元，包含按季發放的伙食津貼，通過三個月試用期考核後，將再額外提供技術津貼；績效與考績獎金另計，依據組織營收和個人績效表現發放。 ※薪資依據專業能力、工作屬性、過往學經歷等核定。 【為什麼要加入我們】 「五心級職場」兼顧工作與生活平衡 1️⃣純日班無夜班，工作家庭都兼顧 2️⃣️多項福利津貼，照顧員工揪甘心 3️⃣️品牌誠信正直，國泰工作有保障 4️⃣定期教育訓練，多元發展的機會 5️⃣工作環境單純，友善職場超貼心
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    • 國泰健康管理顧問股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • 建築/機電BIM規劃繪圖主任

    年終獎金工作獎金員工聚餐康樂活動

  • 企業名 雙橡園開發股份有限公司
  • 工作地點 台中市北屯區
  • 薪資 月薪55000~85000元
  • 工作內容 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。
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    • 雙橡園開發股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • 法規策略計畫(資深)專員 Regulatory Affairs (Sr.) Specialist
  • 企業名 美時化學製藥股份有限公司
  • 工作地點 台北市信義區
  • 薪資 月薪55000~85000元
  • 工作內容 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
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    • 美時化學製藥股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • 內部稽核 Internal Auditor
  • 企業名 美時化學製藥股份有限公司
  • 工作地點 台北市信義區
  • 薪資 月薪55000~85000元
  • 工作內容 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.
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    • 美時化學製藥股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • SAP(資深)專員 SAP (Sr.) Specialist
  • 企業名 美時化學製藥股份有限公司
  • 工作地點 台北市信義區
  • 薪資 月薪55000~85000元
  • 工作內容 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.
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    • 美時化學製藥股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • 法規(資深)專員 Regulatory Affairs (Sr.) Specialist
  • 企業名 美時化學製藥股份有限公司
  • 工作地點 南投縣南投市
  • 薪資 月薪55000~85000元
  • 工作內容 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.
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    • 美時化學製藥股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

  • 品質系統經(副)理 Quality Systems (Assistant) Manager
  • 企業名 美時化學製藥股份有限公司
  • 工作地點 南投縣南投市
  • 薪資 月薪55000~85000元
  • 工作內容 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.
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    • 美時化學製藥股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

9/16

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