交大專區

01.與國內外客戶互動因應客戶需求開發膠材。 02.化學材料混合與配方研發(樣品、試產、成品)。 03.負責新材(原)料的評估、測試、分析與選擇。 04.熟練掌握化學實驗技巧。 05.材料測量和分析能力，熟悉儀器分析（例如：APC / GPC / DSC / FTIR等）。 06.準確記錄所有實驗過程及數據並設計圖表。 07.在新產品製造階段中進行實驗室研究，並執行操作流程之試驗。 08.研發新的、改良的化學製程。 09.負責新產品或技術的製程開發及導入(試產→量產)。 10.制訂新產品檢驗標準。 11.在生產作業過程中進行相關變項的檢測，以維持一定效率、品質之生產。 12.各國的相關文獻資料收集、研讀。 13.保持實驗室與設備的清潔及維護, 並維持實驗室安全操作規範。 14.負責ISO各管理系統運作。 15.跨部門溝通。 16.完成主管交辦事項。 態度要求 1.工作細心、正確，出席正常、服從指示。 2.將職務所規範的事情做到沒問題。 3.盡力將工作圓滿達成(Cover工作灰色區域)。 ※本公司與政府有配合安穩僱用計畫，請來公司面試前先到斗六就業中心身份認定， 符合資格的人員，經公司錄取，政府會額外補助最高2萬元。 ※社會新鮮人:碩士起新NTD43850，加班費依勞基法另計，有產業相關經歷者另議。 ※年薪約為 14 個月 (月薪12個月+年終獎金2個月，年終獎金年資未滿一年年終依比例計算)。 ※戶籍地外縣市研發同仁可提供宿舍。 ※需視工作情況，配合加班。

1. 設置和操作CNC銑床機台，並且獨立生產加工。 2. 具視圖能力，架刀更換工件 ，準確實現加工需求。 3. 調整加工參數確保精度。 4. 執行產品的量測和品質檢驗，確保符合標準要求。 5. 定期維護和檢查CNC機台，解決常見故障問題。 6. 優化加工流程，提高生產效率和機台運轉效果。 7. 嚴格遵守安全操作規定，維護整潔和安全的工作環境。 8. 與工程師與技術人員協作，處理技術問題並改進設計。

機械加工技術人員 依照工作圖或實樣準備材料、工具、刀具、量具、工具機、研磨齒輪 從事簡易機件製作與加工修配工作

CNC車床人員 精密CNC磨床設備與CNC車床機器操作，進行金屬或塑膠原料的研磨、切割與製型工作 管理委託件之加工進度 ，模具零件加工、刀具採購與管理、負責工件加工處理 協助管理生產流程、控制工件尺寸及品質、加工現場安全監管 負責產品測試與量測，協助改善製程品質與追蹤 車床操作機器設備之保養與維護 製作日報表 (領料數量、加工次數，時間、入庫數量)

工作內容 1.CNC銑床機台操作，包含架模、準備刀具、對刀座標軸 2負責產品測試與量測，協助改善製程品質與追蹤 3.CNC銑床機台的維護包含故障排除、保養等 4.基本量測成品或半成品尺寸、品質控管　　 5具經驗，能獨立作業者 6.程式編寫 7.具視圖能力

1.中央監控整合規劃及維修服務2.E-HOME及雲端住宅整合架設及維修服務3.寬頻網路架設及維修服務4.天線系統架設及維修服務5.車道管制系統整合架設6.門禁系統架設及維修服務7.屋內自備線寬頻窄頻光纖NCC竣工8.監視系統軟硬體設備配線、安裝。 2.光纖熔接.測試施工 3.公司願意培養新人、及輔導考取證照、 無經驗可 ※工作地點：台中市。

1.用者電腦故障排除,軟體安裝、設定、系統操作，與分析網路資料傳輸與網路安全架構等特性，以設計、發展及維護網際網路系統之正常運作 2.安裝、修改、偵錯各種網路安全系統，以防制網路駭客入侵特定之網路 3.支援網路安全系統程式設計工作、及網路及通訊系統整合 4.對網路安全系統之運作、管理及周邊設備之採購作業，提供技術性建議 5.協助客戶進行電腦設備軟硬體安裝 6.透過電話或網路排除客戶端問題、代理產品的售後服務 7.處理電腦相關產品維修、零件及模組更換、升級、保養及故障排除、電腦系統運作的維護及緊急狀況的解除

1.協助ERP專案計畫推行。 2.協助各單位ERP操作之教導。 3.ERP異常狀況及資料處理。 4.協助ERP相關流程、輔導及執行狀況稽核和檢討及反映。 5.協助主管交辦事項。 6.其他文書作業。

※週休二日紅字休 ※無經驗公司可培訓 1.使用檢驗儀器(GC.LC..等)檢測產品理化及物理性質以符合規格要求。 2.來料、半成品及成品之品質檢驗。 3.報告製作。 4.主管交辦之其他事項。 5.無經驗可，歡迎社會新鮮人(需化工.化學或食品相關科系)

1. 計劃、執行維修及保養工作。 2. 設備運轉之效率改善及檢討。 3. 生產設備之即時故障排除。 4. 其他

1. 計劃、執行維修及保養工作。 2. 設備運轉之效率改善及檢討。 3. 生產設備之即時故障排除。 4. 其他

1. 大專以上電機相關科系畢業。 2. 具機電管理施工經驗尤佳。 3. 可配合公司長期培養。

1. 負責工地現場監工、人員調派、工程分包安排及業務處理。 2. 協助丈量尺寸，繪圖，核對圖面資料，並負責圖檔管理。 3. 負責各項行政庶務工作（如：檔案管理、請款）。 4. 協助工地物料管理（如：進貨驗收、庫存盤點）。 5. 聯繫廠商並追蹤工程進度。 6.完成主管交辦事項。

1.有現場操作機械經驗者為優先 2.如具備相關經驗者並能熟悉上手後可提升至調整員 3.需配合加班，加班均有加班費

【應徵本職缺需能配合公司安排出差，主要出差地點為台中地區，必要時亦須支援其他地區（例：台北、新竹、台南、高雄...等）】 1. 熟悉PLC編程和人機介面設計者佳 2. 有機械工程、電機工程、自動化…等相關領域的專業知識者佳 3. 人機介面（HMI）和PLC程式的故障診斷與排除 4. 負責客戶端設備的程式修改或機電零件硬體的安裝、修改、測試及維護...等工作 5. 為客戶提供技術支援（必要時，對客戶進行設備操作和維護的教育訓練） 6. 完成維護和修理後，進行維護記錄和服務報告撰寫 7. 其他主管交辦事項 初期先培訓售服&電控工程師所需各樣技術，將循序漸進逐步教學，並由資深同仁帶領&陪同外出工作，最後獨當一面為客戶端提供售後服務與技術支援。 【本職缺於到職後需至林口總公司進行一周受訓】

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。

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

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. 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.

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.