• 面議(經常性薪資達4萬元或以上) 新竹縣竹北市 工作經歷不拘 7天前更新
    1. 「病毒製程開發與優化」或「病毒檢測方法開發、SOP建立與執行及技轉」。 2. 實驗設計、執行、結果分析與紀錄彙整。 3. 病毒生產與文件撰寫。 4. 支援建廠事務 5. 主管交辦事項 *此職位須於台北內湖受訓,後續配合新竹建廠進度轉至新竹工作*
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    年終獎金三節獎金績效獎金員工團保勞保
  • 月薪30000~55000元 台中市北區 工作經歷不拘 今天剛更新
    1.從事西藥銷售、拜訪、產品諮詢及售後服務。 2.處理客戶疑難問題。 3.收集市場產品資訊。
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    就業保險產假年節獎金員工生日禮金員工宿舍
  • 面議(經常性薪資達4萬元或以上) 台中市南屯區 2年工作經驗 10天前更新
    1. 具備藥局相關業務經驗 2. 市場資訊收集分析、反對意見處理 3. 新開戶開發 4. 客戶分級及區域管理 5. 舉辦Seminar , RTD 6. 推廣及開發OTC指示用藥及處方藥物 *本職務實際業務責任區需依公司分配,以中部地區包含台中、彰化、南投為主。
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  • 面議(經常性薪資達4萬元或以上) 台北市信義區 10年工作經驗 10天前更新
    This position will report to Tax Director of Lotus Group and be actively involved in tax planning, compliance, controls, and reporting with focus in South East Asia. As a key contact person for tax related matters in South East Asia, He/She is expected to maintain constructive relationships with representatives from the Tax Authority and tax consultants. e/She Role & Responsibility of regional tax role: -Manage tax compliance matters including but not limited to corporate income tax, indirect tax, withholding tax, local tax, tax provisioning, and tax accounting -Review and approve the tax returns or filings prepared by local finance or external advisors and ensure tax liabilities are paid in due course; -Partner and manage the relationship with various internal stakeholders such as Controller, FP&A, and functional heads to ensure all taxes (ie. current tax, deferred tax and WHT) are properly accrued and accounted not only for monthly reporting purpose but also for forecasting/budgeting. -Manage tax queries raised by tax office to ensure they are dealt with appropriately and on timely manner. If need be, seek advice from external consultants. -Highlight any contentious tax issues and suggest any practical solutions. -Support and/or educate local financial controllers with the changes in the domestic tax regulations that are impacting their business operations. -Actively support the Group Tax Director in developing the Group’s tax strategy as the business evolved including but not limited to -Assist Tax Director of Lotus Group in implementing strategic tax decisions that drives the Group tax forward. -Identifying opportunities for further enhancement and development of the tax strategy and function. -Proactively contribute ideas that could help to mitigate tax risks and/or optimize tax opportunities for the Group. Skills and Requirements -Bachelor‘s degree in any Accounting Field, preferred with CPA or tax related accreditation. -Minimum 10-15 years‘ experience within an international tax environment, ideally in the Big 4, preferably combined with a few years of in-house experience. Strong experience with a variety of tax operations (such as indirect tax, transfer pricing & tax accounting) and ability to drive process improvements. -Proficiency in Microsoft Office applications, especially Microsoft Excel and PowerPoint, working knowledge of some ERP system is preferred. -Ability to deal with multiple stakeholders across different cultures. -Ability to work independently without much supervision.
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  • 面議(經常性薪資達4萬元或以上) 台北市信義區 4年工作經驗 10天前更新
    1.應收帳款及銷貨收入相關帳務處理 2.業務相關費用審核 3.負責月結/報表編制及分析 4.其他交辦事項
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  • 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 10天前更新
    1. 制定/維護/更新使用於研發專案之臨床批及查登批的所有原、物料之規格及化驗方法。 2. 向原料及物料廠商索取相關文件,如:規格與檢驗方法、原料主檔案、技術文件等;審閱3. 廠商提供之技術文件,如有需要,進一步向廠商索取其他文件進行評估,做適當的整理與歸檔。 4. 協助CMC文件準備,提供主成分、賦形劑、包材之檢驗規格予法規部門,使其可進行NDA和ANDA查驗登記的文件整建作業。 5. 審閱B2B差異清單,並準備成本估算、工作計畫,並依據時程制定時間表,並及時協助B2B專案相關的客戶問題的完整回應。 6. 根據B2B需求準備和審核文件,例如檢驗規格、分析方法、標準操作程序等。 7. 按客戶要求準備CMC文件,使其可進行NDA和ANDA查登的文件整建作業。 8. 協助查廠時與實驗室相關之PIC/S GMP文件。 9. 查廠期間支援QA文件調閱與查核。 10. 主導變更管制之撰寫、偏差事件調查、矯正預防措施之評估與執行。定期更新、審閱及維護部門之標準操作程序。 11. 定期更新/採購各主要國家之藥典公定書。 12. 確保所有活動和分析均符合GMP、正確的程序、法規指南以及健康安全法規。
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  • 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 10天前更新
    Overall Objectives Safety Officer, under the leadership of Lotus PVO (Pharmacovigilance Operations) Head, is responsible for execution of PVO activities in accordance with the Lotus pharmacovigilance quality system and local pharmacovigilance requirements. General Duties • Participates in or conduct daily PVO activities assigned by PVO Head • Maintains an accurate and comprehensive list of the Lotus products which are subject to pharmacovigilance activities by monthly alignment with the Regulatory Affairs teams • Coordinates with Local PV Offices (LPOs), PV CROs and partners or vendors regularly for PV activities • Monitors and tracks the PV activities performed by the stakeholders/LPOs, including, but not limited to: • Screening of local legislation and regulatory safety announcements, screening of local scientific journals for relevant safety information, as required • Maintenance of PV trackers (Individual Case Reports, Medical Inquiry and Product Quality Complaint, Aggregate Report tracker, Risk Management tracker, Safety Data Exchange Agreement tracker) • Updating of PSMF (Pharmacovigilance system master file) and relevant annexes as required • Reviews Individual Case Safety Reports (ICSR) and Medical Inquiries (MIs), as needed • Is aware of the risk management plans approved in their territory and of the risk minimization measures implemented. Assists in ensuring that the required activities are performed and tracked • Assist with the preparation and review of aggregate safety update report (PSUR, PBRER etc.) • Is aware of local safety concerns and supports the signal detection activities by reviewing the outcome of the screening of the local PV legislation and safety announcement, as required • Maintains and files the PV documents filed in the PVO specific folders (hard copy, where required and soft copy) • Coordinates for translation of PV related documents, when required • Tracks received adverse event, MI and PQC. Participates in reconciliation of PV activities between the Local PV Offices (LPOs) and PV CROs or partners or verifies that reconciliation activities are performed as per requirement • Supports in submission of relevant ICSRs received to competent authority within deadline • Participates in regular meetings with PVO and PV CRO as required and in-charge of MOM • Consults PVO Head for any issues or uncertainties relating to pharmacovigilance activities • Communicates with LPOs, PV CRO and other external PV vendors • Informs PVO when contacted regarding agreement involving pharmacovigilance obligations • Supports during audits and inspections • Trains on and applies the Lotus pharmacovigilance SOPs and the applicable PV related regulation • Stays current on the local PV legislation in the Lotus MA countries • Is involved during the development of Lotus pharmacovigilance SOPs • Ensures that all relevant employees in the LPOs receive basic pharmacovigilance training and that training is recorded and archived appropriately • Performs any other PV related activities assigned by the line manager (PVO Head) • Liaise with the stakeholder department or other internal departments.
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  • 月薪40000元 南投縣草屯鎮 2年工作經驗 10天前更新
    1. Responsible for the successful delivery of the assigned project in terms of costs, schedule, resources, and quality. 2. Review and validation of the user requirements develop scope of work and follow up of the bid phase. 3. Responsible for project engineering design. procurement technical evaluation conscruction, T&C, and qualification. 4. Collaboration with stakeholders in the capital workflow to ensure the process is followed from: Team Charter. Scope and URS, Schedule, Cost Estamate and CAR submission. 5. Communication to the Site Management: raising awareness if prnblems come up e.g. mil cstones cannot be reached, costs will be higher than planned etc. 6. Manage external and internal resources used in the implementation of capital projects. 7. Responsible for managing the assigned assigned team and resources through a matrix project organization, including contractors and suppliers. Coordinate the team tasks and supervise the right level of deliveries. 8. To execute tasks as delegated by line manager.
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  • 月薪38948~45624元 新竹市香山區 工作經歷不拘 4天前更新
    1.協助執行農產品冷鏈計畫亮點成果推動。 2.協助辦理計畫座談活動及科研成果產業化工作。 3.協助蒐整國內外農業、冷鏈物流、採後處理、設備技術及法規等相關資料。 4.協助產業調研分析,工作報告撰寫。 5.執行主管臨時交辦業務。 國內外農業、食品、生技相關系所學士(含)以上畢業。 (依法進用保障名額,具原住民身分尤佳) (薪資待遇:大學畢業38,948元、碩士畢業45,624元) 經歷要求: 1.具政府計畫執行或產業座談活動辦理經驗者佳。 2.熟悉科學研究或產業調查者佳。 3.具辦理行銷推廣活動相關經歷尤佳。 4.熟悉國內外冷鏈物流或農產品採後處理者優先。 職能條件: 1.具備良好溝通協調能力與團隊精神。 2.可配合常出差者。 3.具備基本英文聽說讀寫能力。 4.具備良好文案與文章撰寫能力。 5.熟悉Office Word、Excel、PowerPoint等軟體。 6.具汽車駕照佳。 應徵方式: (一)請利用人力銀行投擲履歷或E-mail:hr@mail.atri.org.tw (合者約談,不合者恕不另行通知) (二)面談時請攜帶下列表件: 1.履歷自傳表。 2.國民身分證正本及影本。 3.最高學歷證件正本及影本。(持外國學歷應加附中文翻譯本及駐外單位驗證之證明)
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    產假產檢假良好升遷制度尾牙員工在職教育訓練
  • 月薪40000元 南投縣草屯鎮 5年工作經驗 10天前更新
    1. Create, review and maintain asset list and production flow map. 2. Review project initiation sheet, user requirement specification, scope of work. 3. Establish equipment capacity and capability to oversee the utilization 4. Facilitate capital expenditure process flow. 5. Review write-off capital and submit the plan. 6. Facilitate multiple function teams to define project scope and deliverables. 7. Provide technical recommendations for capital projects 8. Create the documentation for training and instruction 10 Accountable for construction safety and regulatory compliance during project execution. 11 Organize appropriate training and transfer of documentation/ information to operation, maintenance team during qualification phase.
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  • 月薪40000元 南投縣草屯鎮 3年工作經驗 10天前更新
    Responsible for the packaging site cGMP, record, and operation compliance, and elimination of potential risks. 負責包裝現場的cGMP、紀錄、操作的合規性,以及消除潛在風險。 Periodically review and revise the GMP documents(e.g., SOP, etc.) to ensure documentation compliance. 週期性審核GMP文件(如: SOP)以確保文件與流程吻合。 Involved in the cross-function optimization project to increase the process from the quality perspective. 參與跨部門優化專案以期從品質角度提升流程。 1. Responsible for the GMP operation effectiveness on the packaging production sites. 負責包裝現場的GMP操作有效性。 2. Responsible for the site work in progress and AQL sampling following appropriate specifications. 負責現場的製程間管控(IPC)以及AQL取樣符合規範。 3. To perform the line clearance confirmation to eliminate the mix-up risks. 執行清線確認以消除混批風險。 4. To perform periodic reviews of the GMP document for the packaging, provide and proceed to the optimization proposal about the detected gaps. 執行週期性包裝部門相關GMP文件審核,針對偵測到的流程不足提案/執行優化建議。 5 To govern and enforce the cGMP processes, 5S, implemented CAPA, and quality procedures are in place and follow
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  • 面議(經常性薪資達4萬元或以上) 台北市信義區 5年工作經驗 10天前更新
    1. Provide leadership and manage the work activities of direct reports in the area of application development for Commercial-off-the-Shelf applications that includes new solutions and enhancement of existing applications 2. Collaborate with business and key IT stakeholders to plan, prioritize, and schedule applications development and enhancement requests, while providing direction and guidance to the applications development staff 3. Accountable for availability and performance of applications portfolio, including ownership of incidents and release management 4. Drives stakeholder satisfaction by delivering quality applications and support with controlled and planned change management and communicate project status to various levels of management 5. Partner with leaders of other disciplines to ensure proposed solutions align with information, technology, infrastructure, business and security architectures 6. Provide oversight in standards adherence through reviews of project work including detailed technical specifications and application code 7. Proven experience in managing relationships with vendors/consultants, IT teams and internal stakeholders 8. A passion for all things tech and a drive to experiment with new technologies to see where they can benefit the business and staying hands-on technical as well as wearing that team management hat
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  • 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 10天前更新
    1. Facilitate Lot disposition process, reviewing GMP docs and managing timelines. 2. Support day-to-day Quality Assurance - Operations. 3. Perform batch disposition activities within specified timelines. 4. Ensure timely review of batch records, SOPs, investigations, and adherence to quality agreements. 5. Set meaningful goals, metrics for groups, and manage performance. 6. Ensure safe, quality, and timely work. 7. Participate in continuous improvement projects, including QA systems and shopfloor processes. 8. Manage non-conformances investigation and compliance. 9. Ensure quality production and operation in accordance with schedule. 10. Quality Assurance management, covering documentation control, batch record review, investigations, production support, training, and compliance initiatives.
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  • 面議(經常性薪資達4萬元或以上) 台北市信義區 工作經歷不拘 10天前更新
    1、國際/國內永續ESG及公司治理資訊搜集與分析 2、利害關係人溝通:官網建置與更新、利害關係人需求回應 3、永續報告書編製並回覆國際永續評比 4、公益活動洽談及執行 5、公司永續目標進度追蹤 *本職缺為3~6個月短期約聘
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