轉職找工作推薦

  • 行政專案人員

    員工旅遊年終獎金工作獎金休閒設施尾牙或春酒員工聚餐

  • 企業名 鉅田潔淨技術股份有限公司
  • 工作地點 南投縣南投市
  • 薪資 月薪36000~0元
  • 工作內容 1.執行主管所交代的命令及專案 2.處理與主管相關的行政事務，例如:負責公共關係事務、跨公司及部門工作協調、協助專案計劃評估及執行與追蹤、主管會議記錄執行追蹤、董事長及主管交辦事務處理、協助部門預算編列 3.無形資產管理，例如：專利、認證等證書到期續證事宜。 4.協助會議、活動籌備、準備統計報表、書面報告、簡報等資料。 5.參與專案發想，擬訂專案架構及範疇。 6.撰寫計畫書及政府補助案相關資料整理。 7.公司文件檔案的建立及管理
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    • 鉅田潔淨技術股份有限公司-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。

8/17

  • 品保主管(產線擴增需求)
  • 企業名 美上鎂科技股份有限公司
  • 工作地點 南投縣南投市
  • 薪資 月薪36000~0元
  • 工作內容 1.負責公司品質管理系統建置與維護 2.負責ISO系統主導與導入、推行與維護落實品質管理系統 3.規畫品質系統相關教育訓練 4.主導內部稽核活動及外部認證 5.建立品質改善機制與品質改善活動推行 6.客訴處理、作業異常處理、追蹤、改善 7.建置品質工程作業及品質標準的建立與修訂 8.產品失效分析與可靠度分析 9.品保單位人員管理、督導、考核 10.實驗室人員管理、督導、考核 11.檢驗規範制度審核、量規儀器驗收與校正管理 12.供應商管理及製程品質管理督導 13.上級交辦事項之完成與回報。
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    • 美上鎂科技股份有限公司-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。

8/17

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。

8/17

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。

8/17

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。

8/17

  • 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 時薪190~0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－%

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。

8/17

  • 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 時薪190~0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－%

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。

8/17

  • (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37000~70000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,LC-MS 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，LC-MS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 opera
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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。

8/17

  • 需求計畫(資深)專員 Demand Planning (Senior) 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37000~70000元
  • 工作內容 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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    • 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。

8/17

  • 廚師
  • 企業名 赤腳精靈窯烤麵包景觀餐廳
  • 工作地點 南投縣南投市
  • 薪資 月薪42000~0元
  • 工作內容 1.設計菜單，以中西式套餐料理為主 2.依據餐單準備相關的食材並處理備用 3.根據顧客的點單進行烹調 4.員工餐點設計烹煮 5.清理以及保養設備 6.環境衛生整理及維護
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    • 赤腳精靈窯烤麵包景觀餐廳-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。

8/17

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