南投縣轉職工作機會，轉職跳槽推薦工作，提供履歷健診等強化服務|1111轉職專區-第276頁

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
薪資面議（經常性薪資達4萬元或以上）40000~0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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工作適配度－%

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6/6

(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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工作適配度－%

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6/6

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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工作適配度－%

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6/6

製造主任 Production 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37000~70000元
工作內容 1. Manage manufacturing process on the shop floor, handle accident events, and report to managers. Ensure production delivery meet KPI. 2. Oversee the technicians and ensure operations follow SOP, cGMP, and EHS regulations. 3. Recruit, probation, and performance evaluation of technicians, and oversee personnel training program execution. 4. Assist SOP generation/revision and investigation of customer complaint and deviation. In responsible area, manage all equipment, instruments, and tooling. Ensure the status of equipment/devices are ready for use. 5. plan and execute assigned projects. Other works assigned by managers.

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工作適配度－%

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6/6

儲備幹部 Management Trainee
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.協助主管規劃廠房、設備、生產、Artwork、品質制度等運作落實，以提昇部門績效。 2.協助各類專案之規劃與執行。 3.完善人才培訓體系及晉升發展管道。 4.100％藥廠CGMP訓練。

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工作適配度－%

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6/6

包裝組長 Packaging Team Leader
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.按照標準作業程序，執行清線/開線確認 2. 在開始生產之前，批准或驗收開機設定，然後開始生產，並在整個批次生產過程中將產品質量控制在規格範圍內。 3.在負責的生產線中，滿足預先計劃的生產計劃、生產目標，如生產周期、廢氣量、產量、品質目標和商定的供應計劃。 4.負責確保通過標準操作程序和批次生產記錄，按照品質標準和產品規格生產藥品，並確認覆核組員確實執行所有重要程序。 5.確保過程中的質量控制即時進行檢查和測試。 6.確保所有生產和品質以及製造記錄/文件均即時並精確地更新。 7.積極參與對半成品或製成品的所有主要和/或次要故障或不合格的調查，並確保採取商定的措施以防止其再次發生等。 8.訓練生產線組員正確的操作和清潔程序、材料申請，區域清理，結算程序，過程取樣檢查和測試，環境監控，cGMP等方面接受過正確的培訓操作程序和批生產記錄。 9.確保現場工作人員遵守所有安全程序。 10.確保按照預定的時間表和標準操作程序進行環境監控。加入我們的美時製藥產線團隊，讓您的技術熱情得到最大發揮！您將獲得製藥工藝和高品質生產技術的完善訓練及升遷制度，立即加入我們，美時是您製藥成就發展之路的唯一選擇！

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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。

6/6

品質合規(資深)專員 Quality Compliance (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37000~70000元
工作內容 1. Review and enforce adherence to quality standards and agreements. 2. Manage non-conformance investigations and compliance. 3. Oversee GMP and regulatory compliance. 4. GMP Supplier Oversight: -Oversight the GMP Vender Audit Schedule. Ensuring Vendor and Auditor availability (internal/external/consultant) and confirming audit dates with both auditors and vendors. -reviewing supplier audit reports, ensuring they meet Lotus QA Standards and are compliant with Lotus SOPs. -Submitting observation reports to vendors, communicating response timelines and tracking them to ensure timely responses. Review of vendor audit responses and managing the review/editing cycle until responses are acceptable. Requesting documented evidence of closure when necessary and filing electronically and hard copy. 5. Manage quality assurance tasks including document control and investigations.

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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。

6/6

【全台營收最大上市藥廠】【獎金優渥】【冷氣廠房】【免費供餐】製造／包裝技術員 Production Operator
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30000~42400元
工作內容 ※※※擴大徵才，工廠提升計畫完工，製藥產線擴大生產規模※※※ 依廠內標準作業程序和現行GMP規範，按排程和製造批次執行產品製造，工作內容包含： 1. 負責執行產品生產相關工作 2. 負責執行產品之製造 3. 負責生產進度及狀況，確實填寫批次記錄及相關表單 4. 執行設備及工作環境清潔及維護 5. 製程設備操作 (混和、打錠、造粒、充填、熔膠、壓丸、定型乾燥等)及相關GMP文件記錄填寫 6. 包裝機台操作(片裝、瓶裝、盒裝、裝箱等)及相關GMP文件記錄紀錄填寫 7. 其他主管交辦事項加入我們的美時製藥產線團隊，讓您的技術熱情得到最大發揮！您將獲得製藥工藝和高品質生產技術的完善訓練及升遷制度，立即加入我們，美時是您製藥成就發展之路的唯一選擇！

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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。

6/6

品管專員 QC Specialist (歡迎應屆畢業生加入)
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37000~0元
工作內容 1.開發調整分析方法(HPLC, GC, IC...)，協助產品製程開發，分析方法之確校 2.執行實驗室設備3Q 3.研擬審查藥典相關產品規格及分析測試，建立藥典規格 4.操作化學分析儀器進行分析，協助產品放行

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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。

6/6

西餐廳副理 All Day Dining Asst. Manager(力麗溫德姆)
企業名力麗觀光開發股份有限公司
工作地點南投縣魚池鄉
薪資月薪37000~0元
工作內容 1.根據部門的標準監督執行並有效的管理餐廳。 2.注意並提升顧客滿意度。 3.協助主管做好人力及費用成本控制。 4.維持部門內有效的紀律，確保遵循酒店規章制度，儀容和衛生標準。 5.在服務期間保持餐廳良好的形象，特別注意與客人的關係及他們的要求。 6.確保根據酒店的要求和餐廳的操作制度提供高品質的服務，並在有必要時糾正。 7.積極的參加餐廳的佈置和運作促銷活動。 8.顧客意見處理。 9.主管交辦事項。

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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。

6/5

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