轉職找工作推薦

  • 【南投】專業驗光人員 (寶島眼鏡-南投) 面試心得
  • 企業名 寶島眼鏡(寶島光學科技股份有限公司)
  • 工作地點 南投縣南投市
  • 薪資 月薪41000~70000元
  • 工作內容 ◆【工作內容】 專業驗光、配鏡加工，及鏡框鏡片調整、清潔等服務 眼鏡商品介紹、銷售等販售管理 顧客售後服務與關懷 維護門市場所與商品之清潔、美觀 各項門市行政作業與系統操作 各式商品包裝、上架陳列 ◆【需求條件】 視光本科系畢業 具備驗光師、驗光生證照 ※具同業經驗者尤佳 (薪資另議) ◆【休假制度】 排休採取月休9~10天制+特休 ◆【待遇與職涯發展】 完善在職教育 一年兩次透明化檢定晉升制度(晉升立即調薪) 提供驗光人員持續教育積分課程 ※具驗光證照且總年資滿三年以上，可報名儲備經理考核，考核通過者，即具備內部創業資格，並可獲得高額分紅 ☆驗光人員：薪資待遇(含獎金) 驗光師$43,000 ~ $70,000以上 [驗光師保障月薪$47,000前十二個月] 驗光生$41,000 ~ $65,000以上 [驗光生保障月薪$45,000前十二個月] 視光科系應屆畢業者$37,000 ~ $60,000以上 [本科無證保障月薪$41,000前十二個月]
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    • 寶島眼鏡(寶島光學科技股份有限公司)-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。

8/17

  • 課輔老師

  • 企業名 愛美語國際語文教育(聯合徵才)
  • 工作地點 南投縣南投市
  • 薪資 月薪28590~32000元
  • 工作內容 1.指導學童作業，協助輔導加強課業，做課業的複習 2.代替家長照顧學童，處理學童在班內一切生活事務 3.與家長溝通讓家長充分了解孩童學習狀況以及生活狀態 4.處理家長的投訴或者要求，與家長協調解決 5.主題式課程教學、協助外師授課，並協助活動規劃與執行 (如親子活動...) 6.櫃檯行政事務執行
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    • 愛美語國際語文教育(聯合徵才)-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－%

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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

  • 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－%

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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

  • 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－%

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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

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