轉職找工作推薦

  • 日班工程員(作業員) 面試心得

  • 企業名 菱生精密工業股份有限公司
  • 工作地點 台中市潭子區
  • 薪資 月薪40400~42200元
  • 工作內容 一、工作內容：機台操作（需久站），產品檢驗 二、上班時間：「依公司年度行事曆」出勤，平均月休10天，(日班有2小時休息時間) 　　　　　　　日班：07:30 ~ 19:30(依約定工作日薪資40400元) 三、面試方式：請先投遞履歷表，本公司會電話通知面試 四、面試／工作地點：台中市潭子區加工出口區南二路22-1號
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    • 菱生精密工業股份有限公司-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。

6/8

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。

6/8

  • 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40400~42200元
  • 工作內容 1. Responsible for new projects feasibility evaluation and map out the submission strategy for global. Evaluate the product information, lead the discussion with the local RA team to find out the possible submission pathway. 2. Ensure timely new product submission and approvals. 3. Requires well communication skill as a coordinator for Brand Acquisition project between supplier and local RA. Work closely with cross functional team to ensure on-time submission. 4. Monitor the current global submission status and consolidate the submission and approval numbers for management meeting. Specific duties and responsibilities. 5. Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy. 6. Submission and variation experiences in US, EU, APAC markets is a plus. Should handle variation requirement collection, variation strategy evaluation, CMC documents review and variation pack preparation. 7. USFDA Annual report preparation, drug listing, other routine work for US license maintain. 8. Prepare dossier for APAC project submission and modify for ROW submission. 9. Support on the clinical part review, with the help from CRO for APAC project. 10. Responsible for dossier audit for in-license products, and prepare the technical audit report.
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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。

6/8

  • (資深)分析研究員 (Sr.) Analytical Researcher

  • 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40400~42200元
  • 工作內容 1. Develop analytical methods, perform analytical tests, and assist the RD team in screening formulations for the NDA and ANDA drug development. 制定分析方法，進行分析測試，並協助RD團隊篩選用於NDA和ANDA藥物開發的製劑。 2. Follow laboratory SOPs and ensure GMP compliance. 遵循實驗室SOPs並確保符合GMP規範 3. Prepare technical documents and review data for the R&D projects and drug submission. 為研發專案和藥物開發準備技術文件並審查數據 4. Responsible for performing the R&D tasks and projects, such as analytical method development, method validation, formulation screening, raw material tests, finished product release, stability study, and dissolution testing.負責執行研發任務及專案，例如分析方法開發、方法確效、配方篩選，原料測試、成品放行、安定性研究和溶出度測試。 5. Use and maintain analytical instruments, GC, HPLC, UPLC, Dissolution Tester, Titrator, Particle size analyzer, etc. Research, diagnose, troubleshoot, and identify solutions to resolve analytical instrument issues. 使用和維護分析儀器，GC，HPLC，UPLC，溶出度測試儀，滴定儀，粒徑分析儀等。研究，診斷，故障排除和識別解決方案以解決分析儀器問題。 6. Train, lead, and supervise junior analysts in day-to-day laboratory operations. Support relevant departments and vendors to complete projects on time, ensure the work and analysis comply with GMP and SOPs. 訓練、領導並監督日常實驗室操作中的初級分析師。協助相關部門和供應商按時完成專案，確保工作和分析符合GMP和SOPs。 7. Review documents, prepare the analytical study report and CMC documents 審查文件，準備分析研究報和CMC文件 8. Responsible for establishing, maintaining, and updating the specifications and test methods for in-process and finished products in the pre-approval phase. 負責核准前半成品和成品試驗相關之檢驗方法與規格之制定、維護與更新。 9. Support assigned responsibilities to maintain GMP compliance of the chemical laboratory, as applicable. 依據分配責任，維持化學實驗室運作皆符合GMP規範 10. Promptly complete work and tasks assigned by superior 及時完成上級下達的工作和任務。 11. Support for analytical method transfer to analytical control, QP sites, and other receiving laboratories. 協助將分析方法轉移到分析控制，QP所在地和其他接收實驗室。 12. Cooperating with PD & RA, complete and all lab tests. 配合PD及RA完成各項化驗項目。 13. Ensure analysis can be conducted with efficiency and completed on time 確保分析工作得以高效率及迅速之進行。 14. Managing and maintaining instrument calibrations, laboratory instrument logbooks, and SOPs. 各儀器設備SOP之制訂、管理、定期維護、校正如期完成。 15. Ensure lab work is conducted according to SOP and complies with EU, US, JP, and global cGMP regulations. 確保其實驗操作皆依照SOP進行，並符合歐美日地區及全球cGMP之規定。
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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。

6/8

  • 研發專案經(副)理 R&D Project (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40400~42200元
  • 工作內容 Under minimum supervision, manage site projects from inception through completion. Most of the projects are new product launches, site transfers, and general operations and supply chain initiatives. The project manager is responsible to work proactively with internal parties and possibly third party to achieve timely resolution of identified issues and ensure all project deliverables are completed according to established schedules. He/She is responsible to develop project plans to facilitate successful project completions and to manage and drive project activities including project planning, internal/external communications, project task assignments & follow-up, etc. He/She must also facilitate problem resolution and issue escalation. 1. Establish project plan with project leader, define critical path and milestone till regulatory approval and manage regulatory extension 2. Propose R&D budget for the project, coordinate with Portfolio team for business case preparation and approval 3. Drive execution of the project in a manner that meets delivery performance goals/objectives and the agreed plan without compromising project deliverables or relationships along with Project Leader and implements the Stage Gate systems for good governance. 4. Propose strategies to bring project cost and timeline down with risk mitigation strategy and efficient resource utilization. Present key operational metrics and maintains the Project dashboard on a real time basis 5. Leads team in the preparation, implementation, & maintenance of risk management plans for projects 6. Responsible for ensuring effective, accurate and timely communication of project information
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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。

6/8

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。

6/8

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。

6/8

  • 職業安全衛生管理師

  • 企業名 茂順密封元件科技股份有限公司
  • 工作地點 南投縣南投市
  • 薪資 月薪35000~55000元
  • 工作內容 1.規劃、制定及執行安全衛生政策、計畫、程序書及標準。 2.執行年度各項職業安全衛生管理系統相關業務。 3.負責安全衛生督導及稽核(巡視、定期/不定期檢查、重點檢查等)，及後續評估分析與建議。 4.維持推動ISO 45001職業安全衛生管理系統 5.其他專案協助及主管交辦事項。
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    • 茂順密封元件科技股份有限公司-使用1111轉職專區 https://central1111.com.tw/turn/
應徵
工作適配度－%

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。

6/8

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。

6/8

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。

6/8

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