求職議題

1.進行烹飪實作教學。 2.設計及開發相關課程，運用適當教學策略與方法，提升學習興趣。 3.上課講義編寫、製備食材與包材。 4.輔導學生考取證照、提供創業管道。 5.觀察學生上課學習狀況，並且針對學生的問題給予解答。 6.評估學習成果並給予意見及鼓勵。 7.輔導學生製作美味成品，使學生獲得成就感。

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。

METROLOGY台灣黑馬牌致力於提供高品質精密測量儀器，是精石公司自創品牌。我們的產品涵蓋精密測量儀器、校正設備、二次元影像量測儀、三次元座標測定機等相關設備，並且已完全打開國內市場並成功外銷至歐洲、美洲、東南亞等100多個國家，成為廣大客戶信賴的合作伙伴。 公司連結：https://www.metrology.com.tw 🌟｜【業務主任】我們正在尋找充滿熱情與專業的你，與我們共同拓展國內市場版圖！ 💬 / 工作內容： / 1. 制定並實施國內市場拓展計畫，深入分析國內市場和潛在商業機會，達成公司銷售目標。 2. 開發新客戶並維繫現有客戶的長期合作關係，提供專業的產品諮詢及技術支援服務。 3. 分析市場趨勢和競爭對手，準確輸出市場所需的銷售策略及競爭方案。 4. 負責報價、合約籌備及執行，跟進訂單進度，確保交期符合客戶需求。 5. 推廣精密量測 儀器校正 硬度測試 等設備行銷與代客第三者公證服務 6. 參與國內展覽會及市場宣傳活動，展示公司品牌產品優勢，提升市場認知度。 7. 製作銷售分析報表，定期檢討和優化銷售策略，助團隊完成業績目標。 8. 提供內部各部門相關銷售數據及分析，協助跨部門協調以促進業務營運流程順暢。 🚀｜加入我們：｜ 我們深知每一位加入METROLOGY台灣黑馬牌的夥伴都是推動企業成功的重要力量。成為我們的一員，您將擁有符合您專業與熱情的舞台，與我們一同將高品質精密測量儀器推向國內外全球市場！準備好迎接挑戰了嗎？現在就投遞履歷，期待您的加入！

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.

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.

1. Evaluation of submission feasibility for in-licensed products (major) and domestically manufactured products in the APAC region (KR, TW, HK, SG, MY, TH, VN, PH, and ID) 2. Coordination of the due diligence and production of the gap list 3. Evaluation and plan of the design, the budget, and the timeline for the bioequivalence study, the bridging study, and the clinical study in KR and TW 4. Communication with the APAC regulatory teams and partner companies to resolve the submission gap in the target markets 5. Design and consolidation of the regulatory strategy of the key milestone, the submission pathway, the submission timeline, and the launch timeline in the target markets 6. To review the License and Service Agreement 7. To support new submissions in Taiwan 8. To update of the APAC regulations 9. To prepare the consultation materials 10.To provide the justification materials on the non-clinical and clinical studies for the deficiency letter 11. To compile the ACTD format from the CTD format 12. To monitor submission progress on all company‘s projects 13. To provide improvement plans 14. The other tasks 1. 協調法規相關部門與供應商評價授權產品 2. 評估產品於亞太地區註冊之可行性，準備註冊所需相關技術文件與試驗 3. 在產品開發及送件準備期間提供法規要求的指引，協助其符合國際法規 4. 即時提供註冊用產品主檔案 5. 協助提供法規更新計畫 6. 即時支援產品維護用技術文件 7. 協助擬定合理且經濟可行之註冊計畫 8. 協助執行註冊計畫

1.熟悉品管手法及具備相關技能,英文佳 2.具工程能力,有壓鑄經驗佳 3.負責各製程生產良率提升及試產.量產時的產品異常分析改善 4.負責從供應商到用戶端的整體品保系統建立.執行與完善及維持公司相關ISO/TS體系的落實 5.負責品保組織人員能力的建立與提升,建立品質KPI目標,協調相關單位提升品質及目標達成 6.與客戶互動掌握客戶需求並落實到製程,確保最終用戶端的品質滿意度 7.檢具及檢驗方法的確認及整合,降低測量時間,製程Traceability的建立與執行 8.具有問題分析能力與持續改善專業能力 9.有品保可靠度系統驗證運作經驗

1. 維修及安裝工廠水電相關設備。 2. 天車及自動機台設備維護及故障排除。

1.協助幼兒學習自理生活。 2.提供幼兒日常生活的照顧。 3.維護幼兒在園所之安全。 4.教授幼兒課程。 5.配合幼兒發展狀況，設計、撰寫課程教案。 ※需為幼兒保育/教育相關科系畢業.並具備幼兒園教師證

美語老師實務內容如下: 1.教授兒童美語課程. 2.教授輔助之美語教材. 3.配合相關教學活動. 4.課程介紹及教育訓練. 5.其他主管交辦事項. 應徵者需有兒童美語教學經驗.

1. 機械組裝/車床/铣床/焊接/切割/能獨立作業

本公司主要銷售發酵機、碎木機和掃地機...等等 1. 輸入、處理並追蹤客戶訂單，並將訂單資料存檔備份。 2. 保持與客戶間之聯繫，回覆e-mail，並確認交貨期。 3. 提供出貨文件，協助業務人員控管出貨，並處理進出口事宜。 4. 定期提供業務銷售狀況報表，以供業務人員或主管參考。 5. 協助業務人員處理銷售業務相關之公司內部行政作業。 6. 客戶書信往來，業務資料翻譯 7. 客戶服務系統之執行與維護 8. 客訴管理與執行 9. 執行主管交辦事項 10. 出貨報關行、船運和客戶聯繫

1.依據設計圖建置建築及水電管線建置3D模型並轉成Cad施工圖面 2.正確在施工圖上標註尺寸、規格需求、材質、施工裝卸順序 3.水電及其他工程之工作圖繪製 4.模型動畫導出

工程師1名為監督水電空調消防及其他工程現場施工