台大就業專區

1.理貨、出貨作業 2.原料及成品出入庫作業 3.主管交辦事項 低溫作業，具備堆高機證照者，另加給

托育不再是「高風險、低保障」的工作了！ 在舜云，我們給你完善工作制度、系統性教學工具，最重要的是溫暖與尊重。 【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。

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.負責電話接聽、轉接、答覆問題及登記留言 2.旅客接待、辦理住房與退房作業 3.提供旅客旅館、觀光等諮詢服務 4.帳務核對 5.工作環境整潔維護 6.其他主管交辦事項 **每月另有獎金制度：時段性住宿達成獎金2,000元、業績達成獎金2,000元**

1.負責電話接聽、轉接、答覆問題及登記留言 2.旅客接待、辦理住房與退房作業 3.提供旅客旅館、觀光等諮詢服務 4.帳務核對 5.工作環境整潔維護 6.其他主管交辦事項 **每月另有獎金制度：時段性住宿達成獎金2,000元、業績達成獎金2,000元**

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.機構零件採購(詢比議價) 2.下訂單及物料跟催 3.需具有採購經驗 4.熟鼎新Tiptop系統尤佳

處方調劑 衛教及藥物諮詢 藥品管理與藥事行政 診所調劑室環境維護

1. 協助設計製作平面文宣、海報、DM 等視覺素材 2. 協助進行設計文案發想與素材整理 3. 協助設計師規劃專案資料、簡報與提案準備 4. 協助審核加盟店提供之CI（企業識別）基本資料 5. 協助品牌商品包裝、週邊物件設計作業 6. 配合執行大型活動視覺素材延伸製作（如背板、立牌等） 7. 處理一般文書與行政庶務支援 8. 配合完成主管交辦事項 加分條件（非必要）： • 具攝影、影片剪輯經驗者尤佳 • 有不動產或B2B相關服務經驗者加分 我們希望你具備： • 基本美感與設計軟體操作能力（Photoshop / Illustrator / Canva 等） • 細心負責，能夠主動溝通協調 • 對設計產業有熱情，願意學習成長 合適者將於7個工作天內主動聯繫，不合適者將不另行通知，謝謝您。

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。

1.製造過程中之製程巡檢、實施品管計畫 2.原物料、半成品，成品、出廠之品質檢驗以及判定 3.不合格品原因之追查、分析、報告以及處理 4.其他以面談內容為主