托育不再是「高風險、低保障」的工作了！ 在舜云，我們給你明確的工作制度、系統性的教學工具，最重要的是透明的晉升管道以及完善的支援系統。 【托育人員｜穩定升遷｜結合音樂與教保的創新系統】 我們是一間結合音樂與教保專業的托嬰中心，致力於提供0～3歲寶寶高品質的全日照顧與啟發性教學。 誠摯邀請有愛心、有耐心，願意陪伴寶寶成長的您，加入我們的教保團隊，一起打造溫暖又專業的學習環境！ 【工作內容】 ◆結合本中心獨家「音樂寶姆系統課程」，提供0～3歲嬰幼兒日常照護與教養服務。 ◆協助引導嬰幼兒身心發展的活動，啟發其感覺統合、智能與音樂潛能。 ◆培養嬰幼兒良好的生活自理能力及規律作息習慣。 ◆關注嬰幼兒身心安全，執行日常安全檢查與突發事件應對。 ◆觀察並記錄寶寶的學習與社會互動表現，鼓勵參與與自信建立。 ◆配合中心活動，參與團隊合作與園內外活動。 ◆完成上級交辦之其他教保相關事務。 🚀不想止步於此嗎? 舜云還有待遇更好的音寶師職位等你來挑戰 專業技能只要你想學，我們就願意教 優渥薪資只要你有能力拿，我們就敢給

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. 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

協助考生找到目標 考上公務員 成為別人的貴人 1. 負責課程推廣與招生規劃，提升招募效率並達成招生目標。 2. 監控課程品質與學生滿意度，定期進行數據分析與成效報告。 3. 管理櫃檯接待與學生事務，維持運作流暢及服務品質提升。 4. 撰寫數位行銷內容，規劃多平台品牌曝光策略與執行計劃。 5. 經營社群媒體並追蹤成效，分析數據提升市場滲透率與影響力。 6. 負責財務會計管理，處理課費收取及帳務精準對核作業。

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.進料(加工料件)及製程巡檢 2.品質管理及異常處理分析 3.出貨檢驗

1.負責ERP相關系統程式：ERP(鼎新)，BPM(鼎新)、MES、看板、智能倉儲、SCM，維護與開發工作 2.負責客製程式修改與協助導入工作 3.跨部門溝通協調能力佳 4.積極進取、細心負責、服務熱忱 5.無經驗可，限資訊科系畢，具程式開發經驗

1.聽從工地主任或領班的調度 2.其他主管交代事項 有經驗者佳

1.掃街車、灑水車、緩撞車、吊卡車...等 2.清潔車輛、例行性檢查 ●駕駛吊卡車須聽從工地主任或指揮人員的調度，進行重物吊運 ●操作吊卡車及起重機相關設備 ●車輛的定期檢查、保養 ※具備移動式起重機證照佳

高速公路道路工程 1.掌握施工狀況 ，配合工地主任交辦事宜 2.負責工程事務規劃 3.監控工地事務以達流程順暢，符合相關法規定 4.現場測量.放樣.尺寸確認 ※具備營造業甲種勞工安全衛生業務主管、公共工程品管工程師(土建組)佳

氬焊.CO2電焊技術人員 安裝及焊接

高速公路道路工程 1.現場施工進度安排與掌控 2.工程成本掌控 3.工地環境維護、工地周邊協調 4.施工相片拍照 5.配合工程會議參與 ※具備工地主任證照佳

1.工程現場勞工安全衛生之規劃、執行、檢查，配合內外業作業 2.施工安全衛生，自主檢查，安全宣導，安全措施 3.工作安全與衛生標準查核作業 4.事故通報與報告 5.處理突發之勞工安全衛生事宜 6.建立勞工安全衛生作業流程、規章及表單 7.其他主管交辦事宜 8.需有乙級勞工安全衛生管理技術士證照 ※需會駕駛手排車(必要)

1. 設計師、美編、美工等相關人員。 2. 本類人員主要從事商業展場設計.舞台布景、櫥窗設計，等商業設計工作。 3. 提供設計發想並完成案件設計、工程等相關事宜。

1.美術編輯溝通協調版面設定，進行平面排版工作 2.展場及活動視覺設計 3.平面設計、平面廣告設計和網頁設計