台大就業專區

1.大型機械設備設計，3D軟體建模。 2.依產業動向需求開發自動化設備，實務拆繪並改善機構功能。 3.結構強度分析與設計。 4.整廠整機設備Layout規劃。 5.歡迎社會新鮮人 (製圖、機械相關科系可)

1. 負責 CNC 加工機操作，機械零件加工。 2. 有傳統加工概念之基礎，有操作經驗。 3. 有加工程式撰寫經驗。 4. 能獨立作業者佳。

1.操作雷射切割機台 2.基本機台故障排除、維護、與保養 3.與其他生產同仁相互協調、配合(折床、木工機等生產機械操作協助) 4.完成主管交辦事項 5.具繪圖、識圖能力

1.負責客戶接洽聯繫及報價資料、訂單處理 2.出貨報關等國貿作業，有船務基礎經驗佳 3.售後服務處理 4.生產進度追踨 5.ERP單據處理 6.主管交辦事項

1. 負責CNC加工機台操作：零件加工。 2. 須會編寫程式。 3. 須能獨立作業、具加工問題解決能力。 4. 具傳統加工機台操作經驗者佳。 5. 與日班人員交接、完成主管交辦事項。

【我們正在尋找這樣的你】 1.具10年以上CNC車床加工經驗，擅長程式編輯與加工參數設定 。 2.有現場管理或技術帶領經驗，能獨當一面 。 3.願意傳承經驗，願意帶領團隊共同成長 。 ★★若能會SOLIDWORKS或AutoCAD為加分條件。 1. 編寫CNC車床加工程式，設定機台參數，確保精準加工。 2. 操作與維護CNC機台，排解簡易異常狀況並提升機台效能。 3. 管控每日生產品質，紀錄加工數據，提供改善建議。 4. 改善製程效率，追蹤成效，保障製品符合要求。 5. 負責試產產品加工，確認製程可行性並記錄問題解決方案。 6. 實施樣品量測及規格檢查，確保零件達標設計需求。 7. 檢查加工圖面與程式內容，避免加工錯誤或偏差。 8. 管理加工刀具，進行選擇測試及維護使用完整紀錄。 9. 使用ERP系統進行工單檢核，線上回報生產完工數據。 10. 編制每週設備檢查表，確認機台穩定運行並預防損耗。 11. 配合完成主管交辦事項及團隊協作相關任務。

1.依據圖面規格、數量、材質組裝半成品、成品及尺寸、外觀檢驗、包裝作業。 2.依據組裝成品數量登打MES報工系統。 3.鋼印作業(雷刻、滾字)。 4.手工具操作與機台維護作業。 5.簡易異常處理排除。 6.環境維護與打掃。 7.支援性作業。 8.主管交辦事項。 ★無經驗可★

我們正在尋找一位專業且細心的關務人員，負責處理和協調我們的進出口業務。 如果您對國際貿易有熱情，且有強烈的責任感，我們誠摯地邀請您加入我們的團隊！ 1. 木質包裝(於釘箱作業時，全程進行拍照及資料存檔) & 堆高機 & 拖車(或貨運)聯繫安排 2. 至順豐快遞、Fedex、DHL、UPS...等國際快遞官網安排取件及製作INV & PAK ; 傳輸相關文件至各國際快遞出口文件部 ; 寄出後資料紀錄及E-mail通知收貨方 3. 負責設備及零部件-型錄&用途原理說明文件製做(相關資料搜集、匯整、補充、修改) * 需不定期至林口各個廠區量箱及拍攝實物照片* 4. 處理及核對設備及零部件進出口報關相關資料與文件 5. 聯繫工廠、FORWARD和報關行，進行結關日確認、排船(或空運航班)、簽S/O、文件檢查等聯絡事項 6. 負責進、出口報關之行政作業，並匯整製作報關文件及應付帳款之請款工作 7. 處理進出口押匯、信用狀以及保稅帳務相關工作 8. E-mail回覆(英文讀、寫需中等)、電話接聽 9. 其他主管交辦事項

【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.負責洗、剝、削、切各種食材，以完成烹飪的前置工作。 2.協助測量食材容量、重量及備料。 3.具備調理技能。 4.主廚交辦事項。 * 此職務為朝九晚六班，非兩頭班或需要輪班，職務內容單純壓力小。 * 享有完整考核制度，視工作表現及能力調薪。

1. 設備運轉維護/異常處理。 2. 支援維修/水電/。 3. 主管交辦事項

1.操作並維護各類塑膠紡織網織造機器，確保生產過程高效且順利進行，達到生產計劃要求。 2.根據生產需求，調整機台織造樣式、網子密度、材質等參數，確保生產的網織品質符合標準。 3.進行設備的日常保養、定期檢查與故障排除，確保機器運行穩定，減少停機時間。 4.如具有相關紡織經驗，待遇可依能力協商，並可優先考慮。

1.電話行銷,既有客戶及新客戶電訪.開發潛在客戶，拓展市場，以達成業績目標。 2.定期電訪客戶服務，維繫穩定客戶關係。 3.負責國內業務接洽及出貨訂單處理等行政作業。 4.負責產品報價及產品展示，並處理帳款回收相關事宜。 5.負責業務推廣，宣傳各項業務重大訊息、活動及產品行銷。

1.產品銷售 2.顧客服務 3.開發客戶 4.接洽業務 5.處理訂單 6.技術支援 7.部門管理

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.

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. 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.

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.