轉職找工作推薦

  • (約聘)設計行政助理 Design Admin. Assistant
  • 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 面議(經常性薪資達4萬元或以上)40000~0元
  • 工作內容 1. 協助對內、對外溝通資料彙整 2. 對外溝通簡報設計 3. 公司社群媒體圖像設計製作及文字編撰 4. 協助執行公司官網建置設計與更新、利害關係人需求回應 5. 熟悉 Photoshop / Illustrator 軟體佳 *本職缺為3~6個月短期約聘
  • 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。

9/6

  • 秘書 Secretary
  • 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 面議(經常性薪資達4萬元或以上)40000~0元
  • 工作內容 1. Coordinate schedule, including meetings, appointments, and travel to ensure smooth running 2. Screen and manage mails and documents, and communicate with other departments and staff 3. Prepare presentation decks, materials and meeting minutes, and attend meetings as requested 4. Prepare and manage correspondence, and summarize documents 5. Maintain confidentiality of sensitive information 6. Handle and process documentation and other administrative tasks 7. Prepare reports, plans, and budgets for meetings
  • 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。

9/6

  • (資深)品管專員(Sr.) QC Specialist (微生物Microbiology)
  • 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 面議(經常性薪資達4萬元或以上)40000~0元
  • 工作內容 1. Establish analytical methods of microbial and execute method validation to ensure analytical method accuracy. 2. Issue blank test report for conduct raw material/package material, semi- product/product and stability analysis, sampling and records, to ensure product quality meets PIC/S GMP requirements. 3. Review of project plans and analysis result reports, inspection/test reports, and SOPs. 4. Conduct test on water for production, Total organic Carbon of water system in laboratory systems and microbial test to ensure the quality of the water. 5. Conduct preparations of growth mediums and potency and growth tests of growth mediums to ensure microbial test run smoothly. 6. Conduct bacterial sub-culturing ,culturing, identification and counts to ensure microbial tests run smoothly. 7. Conduct environmental monitoring of production zones A,B and C(bacterial test on air conditioning system to ensure the conditions of production environment meets GMP requirements. 8. Conduct cleaning and maintenance of all instruments and equipment, calibrations/validations and sort yearly assessment reports to maintain normal usage of instruments and equipment. 9. Perform self-inspections or internal audits as required by the audit schedule.
  • 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。

9/6

  • 無菌調劑(助理)工程師(歡迎無經驗且具學習意願者投遞) 面試心得
  • 企業名 國光生物科技股份有限公司
  • 工作地點 台中市潭子區
  • 薪資 月薪31000~35000元
  • 工作內容 1.執行疫苗或其他藥品無菌調劑/配製製程 2.生產線設備準備與操作、例行驗證與確效、第一級預防保養執行 3.作業環境無菌相關準備維護 4.原物料、設備等製程相關請領作業 5.修訂GMP規範相關文件與定期審閱 6.其他主管交辦事項 職缺頁面所列工作待遇為核定薪資 另有其他獎金、津貼,依實際工作狀況於核定薪資外另計(如排班津貼、職場津貼等) 並依生產狀況另提供生產津貼 上述獎金、津貼依公司規範章程現況為主
  • 國光生物科技股份有限公司-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。

9/6

  • 人資專員(捷絲旅) 面試心得
  • 企業名 晶華國際酒店集團
  • 工作地點 台北市大安區
  • 薪資 月薪35000~40000元
  • 工作內容 1.協助人才選訓育留及人資例行事務 2.協助館內教育訓練規劃、執行及成效追蹤 3.負責實習生開發及招募(需配合出差) 4.負責規劃及執行員工活動、員工關懷 5.具飯店相關工作經驗者佳 6.需了解勞動基準法及職業安全衛生相關法規
  • 晶華國際酒店集團-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。

9/6

  • SAP(資深)專員 SAP (Sr.) Specialist (ABAP)
  • 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35000~40000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.
  • 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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9/6

  • 法規主任 Regulatory Affairs Section Lead
  • 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35000~40000元
  • 工作內容 1. Organize regulatory information and track and control submissions, review and advise on submission strategy for compliance with regulatory filings. 2. Evaluate new proposed change from operation team and assessment impact and requirement on regulatory filings worldwide, and research regulatory issues and provide guidance and advice to colleagues and RA team. 3. Ability to provide clear direction and guidance to RA teams and others. To organize, prioritize, and deliver tasks and projects, with a sense of urgency. Ability to organize team works in timely manner with accuracy. 4. Represent Regulatory Affairs on project teams to ensure all regulatory requirements are met throughout the product lifecycle. 5. Regular update RA status in order to align with business objectives, deliver outstanding launches. 6. Keep closer communication with marketing team and related department proactively to get correct and immediate updates of our products. Need to ensure the variation not disturb the inventory. 7. Effective in working with multifunctional team and to fix complex matrices. Strong communication, interpersonal, organizational skills and problem solving skills. 8. Ability to provide clear direction and guidance to RA teams and others. To organize, prioritize, and deliver tasks and projects, with a sense of urgency. Ability to organize team works in timely manner with accuracy. 9. Relocated in Nantou Operation Center for training for above 6months to a year.
  • 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。

9/6

  • 法規(資深)專員 Regulatory Affairs (Sr.) Specialist, New Filings
  • 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35000~40000元
  • 工作內容 Job Summary: This position is based at Lotus Taipei office and involves working closely with the local RA teams to manage the registration for in-licensing products. The role is accountable for RA experiences in new submissions and life-cycle management across both Asia and Southeast Asia. English communicative skills in spoken and writing clearly, concisely, and effectively are essential. This role offers exposure to an international RA environment and facilitates the development of expertise in regulatory affairs and project management. 1. Initiate, coordinate and supervise the registration of medicinal products from the company portfolio through national procedures in the APAC region. 2. Coordinating the evaluation of possible regulatory strategies and provide support for preliminary reviews of new projects. 3. Providing support for samples preparation and dispatch, when necessary. 4. Ensuring all the additional processes relating national submissions (pre-reviews, DMF, PMF and GMP accreditation etc.) are submitted on time and those submissions/approval processes do not delay drug registration. 5. Communicating with third parties in order to expedite submissions and ensure regulatory compliance. 6. Ensuring all responses to authorities’ requests are correct, complete and timely submitted, including the responses to LoDs for the allocated projects as well as the ones related to PI for all the ongoing procedures. 7. Ensuring that accurate and complete information is timely provided to other departments/third parties and inform the relevant functions on the status and progress of the assigned projects in order to meet the set objectives, identify potential problems or delays, and possible solutions, as they occur. 8. Controlling costs and ensure proper internal evaluation and approval for each cost before it is being generated. 9. Providing support for documents and samples preparation for tenders and legal activities related to patents. 10. Coordinating the arrangements for inspections requested by the local authorities. 11. Maintaining the current knowledge of applicable legislation within the responsibility area in line with the most up-to-date provisions. 12. Ensuring that the internal regulatory database applicable trackers and SharePoint locations are kept up-to-date.
  • 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。

9/6

  • 法規專員(台北) Regulatory Affairs Specialist-Variation(Taipei)
  • 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35000~40000元
  • 工作內容 1.藥品安全性監視計畫之執行及嚴重不良反應通報。 Execution of drug safety surveillance program and reporting of serious adverse events. 2.藥品/醫材上市後變更及展延送件 Submission of renewal and variations for drugs and medical devices 3.跨部門溝通 Work closely with project teams. 4.送件資料歸檔及維護 Maintain regulatory files/database and chronologies in good order. Establish and maintain system for tracking changes in documents submitted. 5.其他主管上級交辦事項 Complete assigned tasks
  • 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。

9/6

應徵
工作適配度%

登入 後即可查看

根據履歷表的填寫狀況,智慧分析您與工作的適配程度。

9/6