轉職熱搜工作

●需求條件:須配合加班、輪休排假出勤、具烘焙相關證照者佳。 ●工作內容:攪拌、取片、烘焙、包裝進倉、包裝機設備操作等麵包生產製程各項作業。 ●上班區間:兩班制.須配合輪班排休. ●夜班津貼:50元/時 (PM09:00~AM07:00)

1.機台操作及例行性機台清機保養 2.依據所進入的產業，按照工程師的指示進行設備之設計、發展、施工、裝設、測試、操作、檢驗與維修等工作 3.機台的加工、組裝作業、安排操作程序

♥無經驗可（公司會協助教育訓練）歡迎你的加入♥ - ▶工作內容 1. 汽車、汽車配備和相關保險的介紹和銷售 2. 貸款協助及其他相關事宜 3. 售後服務(安排保養，道路救援，顧客問題解決) - ▶優渥福利 🧧下午茶🧧三節聚餐活動 🧧年終獎金🧧每年國外旅遊(免費) 🧧尾牙🧧尾牙抽獎🧧每月聚餐 🧧團保🧧工作獎金🧧員工優惠

排放管道、環境品質、廢水及地下水、廢棄物採樣工作。 ※科系要求：工科、理科、農科、醫科 ※※ 無經驗可，本公司具備完善的在職教育訓練※※

位於臺北市民生東路與復興北路精華地段商辦，近捷運、公車交通便捷，機車車位停放，安心上下班，歡迎有熱忱的人員一同加入。 -三班制(07:00~15:00、15:00~23:00、23:00~07:00) -依勞基法規定，享特休、事、病、婚、喪等假 -依勞基法規定計算加班費用 -勞健團保、退休金提撥 -年終獎金，另享三節福利 工作內容: 1.辦公大樓管理人員： -安全巡邏、留意進出人員 -櫃檯換證、信件收發 -大樓人員詢問記錄、訪客引導 -其他現場主管交辦事項 2.公司自聘員工，試用期3個月。 3.試用期滿薪資約42,500(200小時)~47,800(220小時)(加班費依勞基法計算) 4.年終獎金依評核表現另計，往年2個月以上

【超越自已，沒有終點】 在金豐盛，績效、獎金無上限，做越多領越多，超越業績目標率越高，獎金領越高！！！ 歡迎具備「業務開發、現貨買賣」經驗人才加入，不限產業背景，一起開拓市場、衝刺業績！ 【你需要負責的工作內容】 1.白肉雞盤商銷售。 2.餐飲、批發、零售、通路開發銷售。 3.定期拜訪客戶，觸發客戶購買意願產生新商機，市場訊息收集、分析業績狀況、擬定銷售策略。 4.產品報價、客戶服務。 5.客訴處理、帳款回收相關事宜。 【職務需求】 1.需自備汽車，公司提供私車公用補助、油資實報實銷。 2.願意配合報到後至台南永康廠實習一週至兩週。(實習期間由公司提供住宿)。 3.願意配合公司出勤休假制度：週一至週六及部分國定假日需配合出勤。 4.本公司主要產品為國產生鮮雞肉，若因個人因素無法接受者，請勿投遞履歷，謝謝。 【加分條件】 具餐飲、食品業銷售、客服經驗者尤佳。

**需配合出差** 負責科技廠無塵室內相關機械設備之組裝及測試完備人員。 負責機台各式零組件組裝，並於組裝完成進行測試確定組裝無誤之工程人員。 無塵室內自動化設備組裝.改造.定位 E84工程 CS人員 自動化設備組裝維修,新進員工(無相關經驗者)會有專人教你 ※需配合加班、休假日需配合上班、需配合出差※

Job Summary: This position is based at Lotus Taipei office and involves working closely with the local RA teams to manage the registration for in-licensing products. The role is accountable for RA experiences in new submissions and life-cycle management across both Asia and Southeast Asia. English communicative skills in spoken and writing clearly, concisely, and effectively are essential. This role offers exposure to an international RA environment and facilitates the development of expertise in regulatory affairs and project management. 1. Initiate, coordinate and supervise the registration of medicinal products from the company portfolio through national procedures in the APAC region. 2. Coordinating the evaluation of possible regulatory strategies and provide support for preliminary reviews of new projects. 3. Providing support for samples preparation and dispatch, when necessary. 4. Ensuring all the additional processes relating national submissions (pre-reviews, DMF, PMF and GMP accreditation etc.) are submitted on time and those submissions/approval processes do not delay drug registration. 5. Communicating with third parties in order to expedite submissions and ensure regulatory compliance. 6. Ensuring all responses to authorities’ requests are correct, complete and timely submitted, including the responses to LoDs for the allocated projects as well as the ones related to PI for all the ongoing procedures. 7. Ensuring that accurate and complete information is timely provided to other departments/third parties and inform the relevant functions on the status and progress of the assigned projects in order to meet the set objectives, identify potential problems or delays, and possible solutions, as they occur. 8. Controlling costs and ensure proper internal evaluation and approval for each cost before it is being generated. 9. Providing support for documents and samples preparation for tenders and legal activities related to patents. 10. Coordinating the arrangements for inspections requested by the local authorities. 11. Maintaining the current knowledge of applicable legislation within the responsibility area in line with the most up-to-date provisions. 12. Ensuring that the internal regulatory database applicable trackers and SharePoint locations are kept up-to-date.