台大就業專區

林森拉娜SPA＆娃娜精品聯合招募 中部區域直營連鎖美容/精品複合式行銷SPA館，唯一培養全方位專職人才，工作環境單純，制度完善健全。 1.協助客戶美容美體售後服務操作.願意協助主管銷售產品或療程及簡易行政、客服等庶務。 2.享銷售+服務獎金抽成，薪資約月領35000~45000元(底薪28590+各項獎金)，收入穩定有保障。 3.工作穩定，可學習一技之長及訓練口才。 4.免費專業技能培訓/實戰經營管理教育、認識中醫理論。 5.提供免費制服、勞健保、6％勞退金、生日禮品、三節禮金、員工購物優惠、國內外旅遊。 6.星期（一〉~（六〉上班時間為上午10：00～下午20：00 星期（日）上班時間為上午10：00～下午18：00

林森拉娜SPA＆娃娜精品聯合招募 中部區域直營連鎖美容/精品複合式行銷SPA館，唯一培養全方位專職人才，工作環境單純，制度完善健全。 1.協助客戶美容美體售後服務操作.願意協助主管銷售產品或療程及簡易行政、客服等庶務。 2.享銷售+服務獎金抽成，薪資約月領35000~45000元(底薪28590+各項獎金)，收入穩定有保障。 3.工作穩定，可學習一技之長及訓練口才。 4.免費專業技能培訓/實戰經營管理教育、認識中醫理論。 5.提供免費制服、勞健保、6％勞退金、生日禮品、三節禮金、員工購物優惠、國內外旅遊。 6.星期（一〉~（六〉上班時間為上午10：00～下午20：00 星期（日）上班時間為上午10：00～下午18：00

1.生產排程安排、排定生產計劃、交期協調、進度控管、交期聯繫及跟催。 2.機器、設備、人員、物料等排程之效率管理與生管流程改善。 3.善溝通協調。 4.須具備基本機械識圖能力 5.無機械相關工作經驗可

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

1.上班地點分為：大發工廠、鳳山門市 2.公司主要為6.8噸箱型貨車、8.5噸升降尾門貨車 3.安排當日工作時間內可完成貨品上車及送出、自行調整午餐休息時間、送貨結束後準備隔日計劃 4.協助注意車輛的狀況、保養、車輛檢驗......等相關工作 5.每日大發廠回來門市一趟供應零售貨物及鄰近縣市送貨主力客戶為主 6.享有同級大貨車工作的福利卻不用南、北辛苦奔波正常上班時間內完成工作 7.送貨數量較多時或是特殊下貨狀況都由2位司機同車配合

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**

無論您有沒有相關工作經驗，只要您對運動有熱忱、有企圖心想跳戰高薪，都歡迎成為我們的夥伴! 《健身諮詢專員的工作日常》 1. 帶領訪客參觀俱樂部環境、各項服務介紹 2. 會籍方案內容講解及銷售 3. 館內會員服務經營、問題處理 4. 館外市場通路開發、公司企業專案推廣 5. 協助更多人養成運動習慣 ▋我們希望您擁有的特質： 1. 邏輯思考與樂觀的心態 2. 溝通能力與靈活人際互動能力 3. 主動積極 4. 熱愛運動＆認同World Gym品牌理念：將運動帶到世界每個角落 ▋一定不能錯過加入WorldGym這個大家庭一起工作 1. 輕鬆工作氛圍，同事都超好相處 2. 不定期部門聚餐、出遊 3. 每年提供免費健康檢查 4. 春酒百萬抽獎 5. 免費進入WorldGym俱樂部運動 ▋工作內容相關影片參考：健身諮詢專員的工作日常 https://www.youtube.com/watch?v=JfvQUBLmWZg

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

1. 進行物流及其他通路之配送、裝卸等的工作人員。 2.有開過11噸以上自用職業大貨車優先錄取。 3.獎金另計

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。開發潛在客戶，拓展市場，以達成業績目標。 ２。課程講師。 ３。國內業務接洽及訂單處理。 ４。產品展示並處理帳款相關事宜。 ５。線上業務推展，傳達及說明公司各項業務重大訊息、活動及產品。 　　薪資41600以上~ 　　對帶組織領管理訓練工作有興趣者

1.負責部門相關文件之整理，建檔以及追蹤 2.完成業務主管其他交辦事項 3.協助業務完成報價等工作 4.顧客連絡資料整理 5.訂單之處理及整理

1.廢水處理及設備操作，維修保養 2.廢水排放水質監控，符合污水排放標準 3.負責設備維修、巡檢、保養、整頓、異常排除、故障檢修等工作 4.具有相關證照，能獨立作業 5.主管交辦事務處理