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職缺名稱公司名稱上班地點工作經驗更新薪資待遇
- 面議（經常性薪資達4萬元或以上） 台北市信義區 3年工作經驗 3天前更新展開
1. Plan and execute internal audits and special projects to evaluate the risks and the effectiveness of related controls. 2. Prepare reports for each engagement and communicate audit observations with corporate, regional, and local management. Apply problem solving skills to issues and provide practical and constructive recommendations. 3. Develop credibility and trust with operating functions to value-add internal controls and management. 4. Monitor changes in Company policies and procedures to align with the applicable Regulations, Standards, and industry practices.
- 面議（經常性薪資達4萬元或以上） 台北市信義區 6年工作經驗 3天前更新展開
1. Support and facilitate business user‘s requirement to seamlessly running at corporate SAP system in the landscape via analyzing, designing, and developing. 2. Work closely with the team (other SAP developers, infrastructure & system teammates) to understand business needs and deliver features in good quality at timely manner. 3. Be capable of creating and assessing software architecture/designs with multiple stakeholders. 4. Manage overall change request and/or incident backlog for the owned topics and ensure the high quality of corrections and notes for the owned topic areas and of stable assist packages with no regressions. 5. Exhibit learning agility by quickly upskilling on new tasks and concepts. 6. Assist our business users during product deployment, critical operations, and system rollout via standard infrastructure, creating maintenance notes and documentation. 7. Will be providing presentations and workshops.
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 1年工作經驗 3天前更新展開
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
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 5年工作經驗 3天前更新展開
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.
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 10年工作經驗 3天前更新展開
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.
- 月薪37000~70000元 南投縣南投市 工作經歷不拘 3天前更新展開
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
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 3年工作經驗 3天前更新展開
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.
- 月薪29000~32000元 高雄市燕巢區 工作經歷不拘 3天前更新展開
1.維護日常操作表單紀錄。 2.污廢水系統設備操作保養。 3.例行性巡檢紀錄抄表。 4.污廢水設備故障排除。 5.實地進行環境整頓。 6.安全衛生設施定期檢查並維護之。 7.現場之設備驗收、設定、測試、保養及日常操作。 8.現場水質基本檢測。 9.其他主管交辦事項。
年終獎金三節獎金國內旅遊尾牙員工在職教育訓練 - 月薪29000~33000元 高雄市路竹區 工作經歷不拘 4天前更新展開
1.環境整理 2.每日設備操作回報 3.例行性巡檢紀錄抄表 4.水措設備操作維護 5.水質檢驗 6.填寫操作紀錄 7.其他主管交辦事項
年終獎金三節獎金國內旅遊尾牙員工在職教育訓練 - 月薪38000元 桃園市龍潭區 工作經歷不拘 55天前更新展開
1. 熟悉公司規章及客服作業流程 2. 傾聽並能迅速回覆顧客問題解決客戶疑問 3. 依據系統圖或電機圖進行設備的維修，更換零件或按裝新的控制器 4. 根據原安裝圖重新組裝已修復設備，並對其進行測試
年節獎金年終獎金三節獎金員工撫恤伙食津貼 - 月薪28590~28590元 新竹縣竹北市 工作經歷不拘 2天前更新展開
1.協助內部業務銷售的相關行政流程 2.處理貨單、訂單，建檔和歸檔 3.整理部門的相關文件及追蹤進度 4.協助處理客戶的詢價與報價 5.執行主管與業務交辦的事項 6.處理應收帳款及應付帳款的帳務
員工購物優惠國內、外旅遊補助員工在職教育訓練良好升遷制度產假 - 面議（經常性薪資達4萬元或以上） 屏東縣長治鄉 3年工作經驗 1天前更新展開
【工作說明】 1.維護企業內部人力資源之相關紀錄與系統維護（如：員工個人基本資料、工作說明書、職務輪調紀錄、出缺勤紀錄與績效評核紀錄等）。 2.人員招募邀約面試：履歷篩選、邀約、面試等相關甄選作業 3. 協助新進同仁報到/離退等相關作業 4. 組織及人員異動管理及異動作業執行 5. 協助各部門人才招募專案規劃、執行及推動 6. 協助處理各項人力資源交辦事項 7. 有招募人員經驗
- 月薪35000元 屏東縣長治鄉 3年工作經驗 1天前更新展開
【職責內容】 1. 企業內部使用者訪談及需求分析 2. 規劃系統解決方案並評估可行性 3. 進行業務規劃與流程優化設計，分析潛在需求 4. 管理系統開發進度、驗收與整合測試 【大江生醫 8436 的優勢】 擁有優秀的研發團隊，更與全球學術界接軌，常態交流功能性食品與護膚品領域的創新研究，設置醫藥等級的品質管控實驗室，以有效用的產品以及高價值成本，為品牌客戶創造競爭優勢。為配合高速自動化生產設備的產出，人工檢驗的速度與品質已不符需求；我們不斷開發高規格生產品質以達到工業 4.0 概念，達到數位製造產能極大化，大江將運用 AIOT 打造無人智慧化工廠。 TCI 榮獲2019天下雜誌2000大調查經營績效50強第5名為前10名內唯一生物科技企業這份榜單綜合2016-2018過去三年營收、獲利及股東權益統計分析，代表2018年展現強大營運爆發力的公司! 【戰略部門 IT 藍圖】 大江生醫將打造生技業軟體服務頂尖的 IT 團隊，數位化轉型提高獲利能力的時代己來臨，我們將打造數位化供應鏈、工業人工智慧、大數據與分析、雲端化創造價值，提昇我們工廠產能、為公司獲利。 今年目標將增員至50位團隊，我們需要你的加入，強化戰略部門! 【榮耀舞台】 在職期間表現優異，有機會參加大江之星選拔，成為大江之星還有機會獲得豐厚獎金或出國旅遊等機會。
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