1.熟悉欲銷售之產品、公司規章作業流程 2.全程以英文書信語言做顧客市場開發並推銷產品 3.依顧客需求報價及簽約、客戶關係的維護與產品需求服務 4.國外市場開發,產品推廣,尋求全世界國外代理商 5..負責開拓海外市場，尋找國外戰略合作夥伴。 6.市場的開拓 、管理及行銷銷售策略的制定與執行 7..海外客戶電話連絡及書信往來處理及審查出口文件 8..配合生產及行政部門排定出貨車輛、船期或航班

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. 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.

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.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/幼兒教育相關科系畢業.

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.

兼職美語輔導老師 週一 . 三 . 四 . 五 下午3:00~8:00 工作內容: 1.指導美語課業、批改學生作業。 2.值班、監考。 3.美語補課教學。 4.美語電話測試。 5.美語電訪。 6.其他主管交辦事項。

誠徵中年級安親課輔老師,需具備以下資格及條件: 1.有安親課輔班帶班經驗者佳. 2.具愛心,對孩童有耐心. 3.肯學習,做事仔細,具良好溝通能力. 4.具基本電腦技能.

1.核對、處理並追蹤客戶訂單。 2.追蹤客戶款項。 3.協助處理客戶的詢價與報價 4.其他主管交辦事項。 5.學習態度積極、細心有責任感。 6.熟悉基本文書處理（word.excel…等）。

一個月基本授課時數55小時其餘時間協助行政事務 享勞健保、年終、績效....等

1.POS系統收銀機操作、結帳 2.佈置及清理餐桌，為顧客帶位或安排座位 3.答覆客人有關餐飲問題，必要時提供建議 5.記錄顧客所點菜餚，並通知廚房或內場做餐送餐 6.上菜並提供有關用餐的服務 7.營業前巡視餐廳清潔、擺設、備品、用具和設施是否完善 8.負責相關訂餐單據的傳遞、與廚房溝通了解當日菜餚 9.負責意外事件及顧客抱怨的處理，並向主管報告 10.協助主管推展餐廳業務 【公司福利】 *上班免費提供餐點 經營理念:『今日的努力、明日的信譽』及『品質是保證、過程是關鍵』 經營目標: 致力於研發道地的美食，提升顧客的用餐體驗，塑造國際連鎖餐廳的特色. 獲得獎項 交通部觀光局推薦台灣百大餐廳 獲評選為亞洲66家套特色餐廳 高雄十大特色伴手禮 台灣十大美食名廚新秀 獲得國內外媒體一致推薦 我們公司的官網是 https://www.chefteng.com 同時也可以歡迎上我們的臉書粉絲團觀看過去的媒體採訪影片 https://www.facebook.com/ChefTengRG

1.電機工程重電設備安裝工作 2.現場工安措施預防 3.工程工安管理 4.工安文件書寫彙整