1. KA通路之議價、合約與促銷活動擬訂。 2. 通路業績達成、預算控管。 3. 通路年度合作計畫之擬訂。 4. 追蹤與分析銷售績效。 5. 通路新品類/項之導入與維護。 6. 改善陳列增加品類曝光率。 7. 通路總公司客戶客情維繫。 8. 取得市場訊息、情報、數據、資料。
✔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.
1. Manage contract manufacturing organization related activities, project management, daily communication and meeting with vendors, PR/PO/Contract activities, equipment maintenance, material purchasing, and provide product information and communication between OBI and foreign & domestic CMO. 2. Assist with vendor selection perform vendor search, due diligence, facility inspection, and vendor evaluation. 3. Supply management closely with other teams to ensure the production supply suffices for development study and clinical trial requirements and is delivered promptly. 4. Manage technical transfer to contract manufacturing organizations assist R&D in transferring technical information to the CMO. 5. Budget control, including payment and invoice management, ensure the payment on time, and clarify the issue of finance. To be familiar with the ERP system. 6. Troubleshooting the issues in manufacturing activities, actively reflecting on the issue to the supervisor, and solving them promptly. 7. To complete the assignment by the supervisor.
The purpose of this position is to develop analytical assays for small molecule, antibody and ADCs. The incumbent will be responsible for the experimental design and execution of method development, qualification and method transfer in support of drug release and stability testing. And he/she will also take responsibility of performing routine analysis. Work is expected to be done in a compliant manner according to SOPs, regulatory guidelines when applicable. Primary Duties and Responsibilities, including mental requirements of position: 1. Perform testing and report result for HPLC, capillary electrophoresis, spectrometer, or mass spectrometer and general analytical instruments. 2. Execute method development, method qualification and participate in method transfer activities and tests of stability studies followed by supervisor’s guidance. 3. Draft and perform equipment and method validation report with basic regulatory expectations for quality control strategies. 4. Carrying out maintenance for laboratory equipment and environments.
1.協助主管大樓相關事務執行 2.具備基本接待素質，有物業、飯店、專櫃相關服務業工作經驗尤佳 3.與業主及客戶建立良好之溝通管道及客戶關係 4.簡易收支報表 5.櫃檯、迎賓接待，行政相關事務處理 6.喜歡微笑、熱情、有服務業經驗與接待熱忱 7.上班時間0900-1800，排休制