1.具下列學經歷資格條件之一者： (1)教育部認可之大學商學、管理、會計、統計、財務、金融、經濟、財政或法律等相關系所畢業，且已取得學士(含)以上學位證書。 (2)教育部認可之大學非上述相關系所畢業，已取得學士(含)以上學位證書，且具金融衍生性商品、證券、金融、保險等相關工作2年(含)以上經驗。 2.具多益(TOEIC)750分以上、全民英檢(GEPT)中高級以上或同等級英語能力檢定成績證明。
1. 入帳相關作業及申報營所稅 2. 要會基礎電腦（OFFICE等）、會正航或鼎新系統者尤佳 3. 需有記帳經驗、有會計證照者尤佳 4. 處理主管交辦的事務
▍員工福利 ▍ @免費供餐：提供員工餐點，讓工作之餘也能獲得營養及能量補充 @員工飲料：莫凡彼咖啡及各項飲品供你暢飲，補充水份 @最佳貢獻津貼：每個月上班的工時達100小時(含以上)，即可每個小時多加10元的多時津貼 (例：原時薪195元，上班100小時，每小時薪水提升為195元+10元，即為205元/小時) @業績達成獎金：什麼，工讀生也有業績獎金嗎?? * 係金ㄟ，只要達成月目標，兼職夥伴也享有月達成獎金的福利唷 @員購優惠：想要用比市價便宜的價格買到最頂級的莫凡彼冰淇淋嗎? *別猶豫，只要加入莫凡彼集團，就可以讓你享有專屬的員購優惠唷 @專屬消費優惠：可至全台莫凡彼集團餐廳(莫凡彼/尖牙/海壽司)，即可享專屬消費折扣 @聚餐津貼：除了工作，我們也重視團隊的凝聚與歡樂，莫凡彼提供每半年一次的門店聚餐津貼 *吃飯唱歌都是沒有問題的唷 看到這裡，是不是覺得很心動唷，趕快動動你的手指頭，按下應徵的按鈕，加入莫凡彼這個大家庭吧！！ @兼職也有定時調薪管道喔!! 晉升調薪管道透明，每季皆有晉升調薪之機會！
【三商家購】 為三商集團旗下之社區型連鎖超市業者，擁有眾多通路品牌，包括：「美廉社」、「心樸市集」、「Go美廉」及「OFFICE Mart美廉便利架」等，其中「美廉社」為主要核心品牌。 【美廉社】 目前全台有800間門市且持續積極展店中，同時與跨國集團日本住友商事旗下日藥妝品牌Tomod’s，開出複合式店型，員工職涯發展具多元豐富選擇，歡迎對零售業/百貨業/連鎖超市有興趣的您一起加入我們的行列 !! 【提供完善升遷制度】 依據各職務規劃所需之專業技能與課程訓練+實務經驗指導，完成指定課程及通過考核者➠可升遷為門市管理職。 【工作內容】 ①商品管理(陳列/補貨/收貨驗收/銷售服務)。 ②賣場經營管理。 ③顧客服務，客訴處理。 ④收銀結帳服務。 ⑤環境清潔維護。 ※具備服務熱忱、熱情、責任感、客戶導向、團隊合作。 ※工作經驗不拘，無經驗可，或具量販店、超市或便利商店工作經歷者歡迎加入。 ※配合工作地點調動，需具備交通工具﹝腳踏車 or 機車﹞。 【工作時間】 早班06:30-15:30 (休息一小時，可外出用餐) 晚班15:00-24:00 (休息一小時，可外出用餐) ※配合早晚輪班。 ※月排休8-9天。
★您想打發退休生活嗎? ★想在退休生活中找更多樂趣嗎? ★想創造退休生活的亮點嗎? ★只要你身體還硬朗，我們都歡迎您來兼差打工! ★年齡不是問題，溝通沒有距離... ★歡迎愛吃美食，愛自己下廚的大哥大姊加入我們打工的行列 1.短工時4~6hr 排班時段：□12:00~16:00，□18:00~22:00 *可依照個人可排班時段排班。 2.無須相關工作經驗 3.清潔打掃，出餐，備料，收碗，洗碗
1.工作時間：採排班制，每日基本工時4~8小時可排班輪班。 百富通集團 繼 莫凡彼Movenpick後… 全新中式品牌！~滷春秋/黑面蔡” -潮流滷味煮+台灣經典字號 聽到就有點小驕傲 生津止渴的楊桃汁及經典滷味煮，熱拌麵是我們的主打產品！ 急需熱情到不行的你！！ 來來來，你將負責： ．與顧客熱情交流，點餐，細心收銀~ ．擔任廚師的助手，烹飪美味餐點 ．負責洗、剝、削、切，準備食材。 ．還要保持工作環境、設備和餐具的乾淨~ ．學習擺盤、打包及外帶~ 還有還有…餐飲人不容易！面試官都和藹可親~ 滷春秋大家庭歡迎你~
✔薪酬福利 ✔完整培訓 ✔升遷順暢 ✔享受生活 築間餐飲集團，擴大徵才！ 提供具有競爭力的薪資，招募有活力的你✌ 讓加入你的築間更加茁壯幸福☀ 期待您成為我們的一份子❀ 歡迎您的加入✋ 〓〓〓【工作內容】〓〓〓 【外場】 1.顧客服務與接待。 2.點餐/送餐及結帳服務。 3.維持客席整潔。 4.內外場聯繫等。 【內場】 1.食材備置與處理。 2.餐點製作與擺盤。 3.環境及設備清潔等。 ➫加入築間方式 1. 按下【✉應徵】將會有主管審核您的履歷。 2. 通過審核後，請留意陌生來電，主管將會與您安排面試唷！ 3. 通過面試後，主管將會聯繫您報到資訊，歡迎加入築間大家庭♡
【早班薪資】：月薪31.6K-35.8K 【晚班薪資】：月薪37.6K-41.8K (含變動薪資：全勤獎金、加班費等，可達37.5-48K) ✔薪酬福利 ✔完整培訓 ✔升遷順暢 ✔享受生活 築間餐飲集團，擴大徵才！ 提供具有競爭力的薪資，招募有活力的你✌ 讓加入你的築間更加茁壯幸福☀ 期待您成為我們的一份子❀ 歡迎您的加入✋ 〓〓〓【工作內容】〓〓〓 【外場】 1.顧客接待、帶位、桌邊服務。 2.協助點餐、負責送餐、結帳。 3.置桌、收桌及維持環境清潔。 4.內外場聯繫及簡易客訴處理。 【內場】 1.依sop標準執行食材備置與處理。 2.依食安法規執行食材保存及管理。 3.執行內區環境、設備、餐具清潔。 ➫加入築間方式 1. 按下【✉應徵】將會有主管審核您的履歷。 2. 通過審核後，請留意陌生來電，主管將會與您安排面試唷！ 3. 通過面試後，主管將會聯繫您報到資訊，歡迎加入築間大家庭♡
【打工期間】 7/1(一)~8/23(五)不含六日 【打工待遇】 日薪1465元起。 【工作地點】 全台-雙北、桃竹、台中、南高皆有營區 【工作內容】 營隊老師、隊輔 【應徵條件】 只要您有心，本協會有非常完整的教學培訓體系，讓你成為一個受孩子歡迎的講師，精采的班級經營課程，秩序管理，學生行為處理…全部免費培訓授課，全國最用心的教學實戰營，讓您挑戰自己站在講台。 【公司介紹】 中華民國大墩教育推廣協會主要推廣兒童課外教育， 寒暑假北中南各地都有舉辦實體營隊，與距離不受限全台最大的線上課程平台，平日在各小學推廣課後社團，台中為總辦公室；推廣項目有黑科技、偵探、獸醫、建築、烘焙、生物、美語、漫畫、麥塊、無人機、街舞、跆拳、籃球、足球、過夜營隊等多項主軸，至今已服務約200間公私立國民小學 ，約100民間團體(如新光百貨,金門酒廠...)！ 2.務必要在報名表備註:從104得知招募訊息 報名表 http://www.sunn.url.tw/commontable_164-1.htm
【工作內容】 外場- 1.負責帶位、點餐、送餐及聯繫內外場之工作。 2.於客人用餐完畢後，負責收拾碗盤與清理環境。 ※ 當日工時滿四小時即提供員工餐 ※ 需可配合百貨營業時間內排班 ※可配合暑期期間(6/24~9/8)
【工作內容】 1. 現場服務方式與標準作業流程確認與執行。 2. 協調外場點餐與內場提供餐點的順序與速度。 3. 營運現場人力調配、招募與員工訓練執行。 4. 危機問題與顧客抱怨即時處理。 5. 管理門店環境清潔工作執行。 6. 確實佈達公司政策與執行。 7. 營運目標達成及成果分析。 8. 顧客關係建立與商圈經營。 【適合對象】 1. 配合度高主動積極學習 刻苦耐勞 不怕辛苦。 2. 兩年以上餐飲管理經驗。
1. Assess risk in internal controls. 2. formulate the annual audit plan according to the risk assessment results and the mandatory requirements of laws and regulations. 3. Review self-inspection reports prepared by all departments and subsidiaries and submit self-assessment reports along with reports on the correction of defects and irregularities in internal control systems discovered by the internal audit departments. 4. Review audit reports submitted by each subsidiary and follow up on the correction of any defects and irregularities in internal control systems. 5. Execute the approved annual audit plan, including specific tasks or plans required by the management, the board of directors and the audit committee. 6. Follow-up audit findings and corrective actions. 7. Prepare the data and ask for Finance Department’s help to report on Market Observation Post System(公開資訊觀測站) according to mandatory requirements of laws and regulations on Jan., Feb., Mar., May, Dec. 8. Provide advice on improving operational process efficiency and consulting services on the design of internal control systems. 9. Maintains professional and technical knowledge by attending educational workshops, reviewing professional publications and content, and participating in professional societies. 10. Report audit findings to the Chairman and the Board, providing insights on area of strength and improvement. -The job title and salary will be adjusted based on experience. 1. 評估內部控制風險。 2.根據風險評估結果和法令要求，制定年度稽核計畫。 3.審查各部門和子公司編制的內控自評報告，提交內控自評覆核報告。 4.覆核各子公司提交的稽核報告，追蹤內部控制制度缺陷及違規行為的糾正情況。 5.執行核准的年度稽核計劃，包括管理階層、董事會和審計委員會要求的具體任務或計劃。 6. 追蹤稽核結果和糾正措施。 7、依法令要求向公開資訊觀測站申報。 8、提供內部控制制度設計的諮詢。 9. 透過參加教育研討會、查閱專業出版物和內容以及參加專業協會來保持專業和技術知識。 10. 向董事長、審計委員會及董事會報告稽核結果。 工作職稱和薪資將根據經驗進行調整。
1. Independently plans, initiates, and executes synthetic organic chemistry experiments and interprets and communicates results as part of a multi-disciplinary team. 2. Utilizing traditional synthetic chemical techniques, execute routine chemical procedures involving organic chemistry, HPLC, TLC and MS analysis of chemical compounds. 3. Operate a variety of analytical instruments including HPLC, NMR to enable structural determination and purity assessment. 4. Ability to foster teamwork and actively participate in the review of projects with colleagues throughout the organization.
Primary Duties and Responsibilities, including mental requirements of position: 1. Work on projects that involve the screening and engineering the bispecific antibodies to improve their functional activities. 2. Responsible for transient and stable transfection on mammalian cell lines for protein/antibody expression. 3. Responsible for ELISA, immunofluorescence staining, DNA/RNA extraction and purification, cloning and PCR techniques, RNA/DNA sequencing for project requirement. 4. Support coordinating vendors and conducting new vendor search. 5. Perform other items requested by supervisors.
1. Participate and contribute to the implementation of strategies and timelines to ensure a successful clinical or commercial product launch, including oversight of CMOs, manufacturing strategy, priority, and forecasting activities that impact overall drug requirements. 2. Roll out serialization for commercial manufacturing to meet requirements and product traceability. Interface with SC, CMC, AD, RD, Quality Assurance, Procurement, PMO teams, etc. to ensure timely implementation of the requirements. 3. Overview of the manufacturing activities and well-planned for all products. Manage the technical transfer to CMOs, manufacturing drugs for the demand of clinical and commercialization. 4. Having excellent troubleshooting on any issues for completion/accuracy of the product timeline. CMO management globally including common and emergency productions of DSI/DS/DP for target timeline. 5. Interact with cross-functional departments to provide the required information or move forward with the projects. 6. Project management including normal and emergency production of DSI/DS/DP. Manage the equipment maintenance and purchasing the necessary materials. 7. Budget management including payment and invoice management of all CMOs. 8. To complete the assignment by supervisor.
1.Participate and contribute to the implementation of strategies and timelines to ensure a successful clinical or commercial product launch, including oversight of 3PL/4PL, supply strategy, priority, and forecasting activities that impact overall drug requirements. 2. Roll out serialization for commercial manufacturing to meet requirements and implementation of strategies and timelines to implementation of strategies and timelines to ensure a successful clinical or commercial product launch, including oversight of 3PL/4PL, supply strategy, priority, and forecasting activities that impact overall drug requirements. 2. Roll out serialization for commercial manufacturing to meet requirements and product traceability. Interface with CDMO, PMO, 3PL/4PL, Quality Assurance, Regulatory Affairs, BioStats, Clinical teams, etc. to ensure timely implementation of the requirements. 3. In partnership with CDMO teams, develop and implement secondary and tertiary packaging solutions as well as shipping and transport qualifications in accordance with applicable regulations. 4. Working with 3PL/4PL, Distribution, Marketing, and Sales Partners, ordering and supplying drugs for the sites/CRO. Manage inventory of finished drug products. 5. Having excellent troubleshooting on any issues for completion/accuracy of the product timeline. Logistics management globally including common and emergency shipments of DSI/DS/DP/IP, and IRT system review for accuracy. DocuSign Envelope ID: 7C2EC902-3596-43C3-8E5C-61D1A74DC162 6. Develop commercial/clinical supply chain business processes, templates, and SOPs. Serve as a clinical supply subject matter expert for regulatory inspections. Contribute to INDs, NDAs, and other regulatory documents as needed. 7. Manage evaluation/selection/implementation/oversight of packaging, and labeling operations, development and management of distribution or supply agreements, interfacing between the CDMO and Clinical teams to ensure smooth conduct of clinical studies, coordination of import and export, etc. 8. To complete the assignment by supervisor.
1. Support oncology drug discovery programs through design and synthesis of potential drugs. 2. Design and synthesize potential linkers, payloads, and platform for antibody-drug conjugates (ADC) development. 3. Support the synthesis, purification, and characterization of organic compounds. 4. Operate a variety of analytical instruments including HPLC, NMR to enable structural determination and purity assessment. 5. Ability to foster teamwork and actively participate in the review of projects with colleagues throughout the organization. 6. Stay up to date with literature in synthetic chemistry, medicinal chemistry, and ADC field. 7. Must be an independent and self-motivated scientist.
• Represent clinical pharmacology for the assigned study team to support clinical study conduct from clinical pharmacology perspectives. • Translate nonclinical data to human efficacious dose projection. • Design experimental PK or PKPD studies in animal or human to better understand the clinical pharmacology of compound in development. • Conduct Non-Compartmental Analysis (NCA) for nonclinical and clinical PK studies and writing the PK reports. • Work with vendor or perform in-house population PK and PKPD analyses. • Responsible for preparation of regulatory submissions such as IND submission, and response to health authority’s questions with respect to clinical pharmacology.