轉職熱搜工作

1.對應廠商PSW管理、品質管理與異常處置。 2.工程監察、樣件確認與委外品質確認。 3.入料檢查規格作成。 4.ISO文件管理與內外部稽核。 5.儀器校正管理。 6.主管交辦事項。 （應屆畢業生可）

1.與客戶及分包供應商溝通討論，定義 CSIA（網絡安全介面協議） 中的各項角色與責任（R&R） 2.遵循 ISO 21434 標準，與客戶及分包供應商依據 CSIA 在產品生命週期內進行以下網絡安全活動並完成相關產出:功能網絡安全概念、TARA（威脅與風險分析）、溝通計畫、CS計畫、案例、可追溯性監控、事件回應與漏洞管理等。 3.定期監控產品生命週期中的網絡安全風險，並向內部和外部相關方報告任何網絡安全事件與漏 4.定期召開內外部會議，與客戶、分包供應商及內部網絡安全小組討論網絡安全要求、執行進度及工作產出中的證據文件，確保滿足客戶需求。 ※依學經歷、工作年資敘薪

1.電腦文書軟體基本操作。 2.簡單視圖能力。 3.線路的舖設及連接，安裝、維修建築物之電線管路與用電設備測試驗收品檢(公司會教)。 4.配合加班 ※不須證照 ※從大里每日都會有交通車前往芳苑上班

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.

1. ISO 22000:2018 & HACCP 系統作業維護及執行 2. 食品輸入業監控計劃及強制檢驗計劃執行 3. 品檢及品管文件製作及保存 4. 食品業者登錄平台資料維護 5. 其他主管交辦事項 ***2~5年食品衛生管理師或 ISO 22000:2018 & HACCP 系統作業維護 實務工作經驗佳 ***公司概況說明: 韓廣企業有限公司是一家每年穩定中求成長的中小型韓國商品進口貿易商, 其關係企業為ISO 認證食品製造廠, 由國外口主要原物料, 在台加工製造生產; 主要通路遍及連鎖餐廳及賣場. 此職務係為公司擴編職缺, 非常歡迎對食品產業有興趣人員加入團隊, 未來有機會可接觸食品進口及食品製造廠相關專業技能等.

1.電腦文書軟體基本操作。 2.簡單視圖能力。 3.施工拍照及報告製作 4.協助線路的舖設及連接，安裝、維修建築物之電線管路與用電設備之測試、驗收、品檢(公司會教)。 5.依主管指示及配合加班 ※不須證照

1. 製造過程中之製程巡檢、實施品管計畫 2.原物料、成品、半成品等出廠的品質檢定，製程異常處理、不良品管控 3. 品質異常處裡分析及不良品回朔與追蹤管理。 4. 退貨客訴處理流程 5. 製程稽核 6. 擬定年度稽核計劃，執行稽核作業，撰寫稽核報告。 7.主管交辦事項

我們正在尋找一位細心、負責且對品質堅持的品檢人員，加入我們專業且團結的團隊！ 如果你喜歡在條理分明的工作環境中發揮，並對確保產品品質有高度使命感，那麼你可能就是我們在找的人！ 你將負責： ◎ 產品檢驗：依照標準作業流程，對包材進行外觀檢查，確保產品符合規格標準。 ◎ 異常處理與改善建議：發現不良品或異常時，能追查與分析原因。 ◎ 配合主管交辦事項：完成主管交付的各項品管任務，並積極參與品質提升與流程優化活動。 我們希望你具備： ◎ 細心與耐心：面對大量重複性工作，仍能保持高度專注與謹慎，準確辨識問題。 ◎ 良好的觀察力：能敏銳察覺產品微小瑕疵與規格偏差，維護品質標準。 ◎ 溝通協調能力：與生產單位、主管及相關部門保持良好溝通，快速解決品質問題。 為什麼加入我們？ ◎ 穩定專業的工作環境：重視品質與流程的團隊，讓你在穩定中不斷學習與成長。 ◎ 發展機會多元：從基礎品檢到製程優化，你將有機會參與品質改善與跨部門合作。 ◎ 重視員工的努力與貢獻：我們相信每位品檢人員都是維護品牌品質的關鍵推手！ 如果你具備品檢工作所需的細心與責任感，並期待與我們一起提升品質標準，歡迎加入我們，一同打造更卓越的產品品質！

1.負責製程巡檢、成品/半成品檢驗、出貨檢驗，以確保生產品質符合標準 2.規格、毛邊、色差、包裝瑕疵等不合格品的判定和處理。 3.填寫品檢所需相關報表。 4.完成主管交辦事宜。