晉升主管職工作推薦

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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。

7/28

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。

7/28

  • ZB 新竹縣二重埔社區祕書(月薪34,000元) 面試心得

    定期調薪

  • 企業名 良福保全股份有限公司
  • 工作地點 新竹縣竹東鎮
  • 薪資 月薪34000~0元
  • 工作內容 一、處理及完成管理費收取及催繳。 二、處理廠商應收帳款等各項資料。 三、協助總幹事及管委會交辦事項。 四、請款資料及財務報表製作。 五、各類文件歸檔。 六、通知事項之製作及公佈。 七、住戶資料之建檔及更新。 備註： 一、勞健保及6％提撥等依法規辦理。 二、特別休假等依法規辦理。
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    • 良福保全股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
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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。

7/28

  • 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34000~0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.
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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。

7/28

  • 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34000~0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.
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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。

7/28

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。

7/28

  • 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50000~0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.
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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。

7/28

  • 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50000~0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
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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－%

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。

7/28

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。

7/28

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。

7/28

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