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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 工作經歷不拘 3天前更新展開
1. 協助對內、對外溝通資料彙整 2. 對外溝通簡報設計 3. 公司社群媒體圖像設計製作及文字編撰 4. 協助執行公司官網建置設計與更新、利害關係人需求回應 5. 熟悉 Photoshop / Illustrator 軟體佳 *本職缺為3~6個月短期約聘
- 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. Coordinate schedule, including meetings, appointments, and travel to ensure smooth running 2. Screen and manage mails and documents, and communicate with other departments and staff 3. Prepare presentation decks, materials and meeting minutes, and attend meetings as requested 4. Prepare and manage correspondence, and summarize documents 5. Maintain confidentiality of sensitive information 6. Handle and process documentation and other administrative tasks 7. Prepare reports, plans, and budgets for meetings
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 2年工作經驗 3天前更新展開
1. Establish analytical methods of microbial and execute method validation to ensure analytical method accuracy. 2. Issue blank test report for conduct raw material/package material, semi- product/product and stability analysis, sampling and records, to ensure product quality meets PIC/S GMP requirements. 3. Review of project plans and analysis result reports, inspection/test reports, and SOPs. 4. Conduct test on water for production, Total organic Carbon of water system in laboratory systems and microbial test to ensure the quality of the water. 5. Conduct preparations of growth mediums and potency and growth tests of growth mediums to ensure microbial test run smoothly. 6. Conduct bacterial sub-culturing ,culturing, identification and counts to ensure microbial tests run smoothly. 7. Conduct environmental monitoring of production zones A,B and C(bacterial test on air conditioning system to ensure the conditions of production environment meets GMP requirements. 8. Conduct cleaning and maintenance of all instruments and equipment, calibrations/validations and sort yearly assessment reports to maintain normal usage of instruments and equipment. 9. Perform self-inspections or internal audits as required by the audit schedule.
- 月薪31000~35000元 台中市潭子區 工作經歷不拘 3天前更新展開
1.執行疫苗或其他藥品無菌調劑/配製製程 2.生產線設備準備與操作、例行驗證與確效、第一級預防保養執行 3.作業環境無菌相關準備維護 4.原物料、設備等製程相關請領作業 5.修訂GMP規範相關文件與定期審閱 6.其他主管交辦事項 職缺頁面所列工作待遇為核定薪資 另有其他獎金、津貼，依實際工作狀況於核定薪資外另計（如排班津貼、職場津貼等） 並依生產狀況另提供生產津貼 上述獎金、津貼依公司規範章程現況為主
就業保險產假產檢假安胎假家庭照顧假 - 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. 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.
- 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. Organize regulatory information and track and control submissions, review and advise on submission strategy for compliance with regulatory filings. 2. Evaluate new proposed change from operation team and assessment impact and requirement on regulatory filings worldwide, and research regulatory issues and provide guidance and advice to colleagues and RA team. 3. Ability to provide clear direction and guidance to RA teams and others. To organize, prioritize, and deliver tasks and projects, with a sense of urgency. Ability to organize team works in timely manner with accuracy. 4. Represent Regulatory Affairs on project teams to ensure all regulatory requirements are met throughout the product lifecycle. 5. Regular update RA status in order to align with business objectives, deliver outstanding launches. 6. Keep closer communication with marketing team and related department proactively to get correct and immediate updates of our products. Need to ensure the variation not disturb the inventory. 7. Effective in working with multifunctional team and to fix complex matrices. Strong communication, interpersonal, organizational skills and problem solving skills. 8. Ability to provide clear direction and guidance to RA teams and others. To organize, prioritize, and deliver tasks and projects, with a sense of urgency. Ability to organize team works in timely manner with accuracy. 9. Relocated in Nantou Operation Center for training for above 6months to a year.
- 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 3天前更新展開
Job Summary: This position is based at Lotus Taipei office and involves working closely with the local RA teams to manage the registration for in-licensing products. The role is accountable for RA experiences in new submissions and life-cycle management across both Asia and Southeast Asia. English communicative skills in spoken and writing clearly, concisely, and effectively are essential. This role offers exposure to an international RA environment and facilitates the development of expertise in regulatory affairs and project management. 1. Initiate, coordinate and supervise the registration of medicinal products from the company portfolio through national procedures in the APAC region. 2. Coordinating the evaluation of possible regulatory strategies and provide support for preliminary reviews of new projects. 3. Providing support for samples preparation and dispatch, when necessary. 4. Ensuring all the additional processes relating national submissions (pre-reviews, DMF, PMF and GMP accreditation etc.) are submitted on time and those submissions/approval processes do not delay drug registration. 5. Communicating with third parties in order to expedite submissions and ensure regulatory compliance. 6. Ensuring all responses to authorities’ requests are correct, complete and timely submitted, including the responses to LoDs for the allocated projects as well as the ones related to PI for all the ongoing procedures. 7. Ensuring that accurate and complete information is timely provided to other departments/third parties and inform the relevant functions on the status and progress of the assigned projects in order to meet the set objectives, identify potential problems or delays, and possible solutions, as they occur. 8. Controlling costs and ensure proper internal evaluation and approval for each cost before it is being generated. 9. Providing support for documents and samples preparation for tenders and legal activities related to patents. 10. Coordinating the arrangements for inspections requested by the local authorities. 11. Maintaining the current knowledge of applicable legislation within the responsibility area in line with the most up-to-date provisions. 12. Ensuring that the internal regulatory database applicable trackers and SharePoint locations are kept up-to-date.
- 面議（經常性薪資達4萬元或以上） 台北市信義區 1年工作經驗 3天前更新展開
1.藥品安全性監視計畫之執行及嚴重不良反應通報。 Execution of drug safety surveillance program and reporting of serious adverse events. 2.藥品/醫材上市後變更及展延送件 Submission of renewal and variations for drugs and medical devices 3.跨部門溝通 Work closely with project teams. 4.送件資料歸檔及維護 Maintain regulatory files/database and chronologies in good order. Establish and maintain system for tracking changes in documents submitted. 5.其他主管上級交辦事項 Complete assigned tasks
- 月薪35000~50000元 台中市西區 1年工作經驗 3天前更新展開
1.開發潛在客戶，拓展市場，以達成業績目標。 2.定期拜訪經銷客戶，維繫穩定客戶關係。 3.負責國內業務接洽及訂單處理。 4.負責產品報價及產品展示，並處理帳款回收相關事宜。 5.負責業務推展，傳達及說明公司各項業務重大訊息、活動及產品。 6.台中地區業務
勞保健保加班費週休二日 - 月薪37000元 南投縣南投市 工作經歷不拘 3天前更新展開
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.
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 工作經歷不拘 3天前更新展開
1. Responsible for ensuring “Good Laboratory Practices” required for analytical research and development , working knowledge of good development/manufacturing practices of formulation development will be added advantage. 2.Compliance review of API, Raw materials, Packaging materials documentation. 3.Compliance review of Stability data for submission batches documentation at regular intervals. 4.Ensure Document management archival procedure followed in place and support for compliance. 5.Active participate in Internal audit on all functional area pertaining to quality system and compliance and support regulatory audits readiness. 6.Ensure compliance of issuance/document control towards internal/external stake-holders. 7.Compliance review of raw data of Regulatory submission and Audit focused documents ensure error free documentation. 8.Conduct training-based training need identification, co-ordinate internal and external training programs and maintain training records of the team members. 9.Support document review for CTA documents. 10.Review and approve of New Equipment qualifications within R&D 11.Ensure Equipment/Instrument calibration and Qualification/Requalification programs adequacy as per the schedule. 12.Ensure Document compliance review at respective stages of Product development at kick off stage, Pilot Bio, Submission batches and filing stage. 13.Regular inspections on laboratories of development labs of both analytical and formulation 14.Any other responsibilities given Head of the Department /Management
- 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. Utilizing strategic sourcing process to identify, negotiate and implement packaging materials, indirect materials, procurement initiatives to drive cost savings. 2. Align with sourcing team to provide local business requirements and market information to support effective collaborative regional strategy creation and execution 3. Partnering with RD / RA/ NPL, and other Functional groups (Executives, Quality, R&D, Regulatory Affairs, Finance, Legal, Engineering….) in discovery, contract negotiation, optimizing economic value, on-time delivery of product & services, cost management & reduction, supplier & partner risk mitigation, and scope of work development. 4. Develop and implement forward thinking procurement strategies to both optimize spending and minimize risk. 5. Creation of effective preferred supplier program and instillation of organizational discipline on onboarding new vendors. 6. Development of KPIs for strategic sourcing with cyclical delivery which drives continuous improvement. 7. Work at Nantou site at least 2-3 days per week
- 面議（經常性薪資達4萬元或以上） 台中市西屯區 10年工作經驗 3天前更新展開
Managing the Procurement activities and all related activities regarding Indirect Materials, Packaging Materials, Capital, such as strategic sourcing, commercial negotiations, contract administration, and supplier relationship management. 1. Executes the Company‘s Procurement Strategy 2. Responsible and accountable for achieving targeted results, including cost savings 3. Utilize should-cost models for assigned categories that are benchmarked and relevant to the global marketplace 4. Provide market intelligence and price trends to relevant internal stakeholders on a disciplined schedule 5. Lead on sourcing events/RFQ process and ensure the company‘s needs for the materials/service in the category managed are supplied at the right time, in the right quantities and at the right price 6. Build and maintain strong and fair relationships with all external suppliers and all internal stakeholders 7. Develop a contract strategy for each project, including to create, negotiate, monitor and enforce contracted terms and conditions 8. Collaborate internally to drive and develop key performance measures/metrics for Strategic Suppliers and monitor supplier performance against these expectations to ensure continuous supplier improvement 9. Enlist senior management, when appropriate, to help reinforce commitment and involvement from suppliers 10. Develops and maintains a strong supply market knowledge 11. Work at Nantou Site 2-3 day per week
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