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4/23 【代徵新加坡Q Squared Solutions】 Senior Scientist (Flow Cytometry) 流式細胞技術科學家

  • 新加坡
  • 經歷不拘
  • 大學

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. Essential Functions: • Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines. • Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances. • Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel. • Prepares data analysis results for upload to LIMS system under the guidance of senior level staff. • Assists in quality investigations, deviations, and resolution. • Prepares buffers and solutions for analysis, as required. • Assists in the review and update of laboratory procedures and techniques. • Guides entry level staff on routine procedures and supports on-boarding of new staff. • Performs and document calibration and maintenance of laboratory equipment as assigned. • Performs and documents hands on training for other lab personnel in areas of proven competency as assigned. • Assists in the review and development of laboratory procedures and techniques. • Assists in the implementation of procedural changes as assigned. • Notifies inventory staff of supply shortages. • May represent lab team on cross functional projects. • Responsible for clear, accurate, and timely communications with cross functional stakeholders. • Participates in continuing education through self-study, attending training sessions and lectures and meetings. • Supports safety, quality, and 6S requirements and initiatives. • Complies with company's procedures and applicable regulatory requirements. ** Employee Benefit and Salary Structure will follow Singapore Q Squared Solutions Policy.

待遇面議 外商公司
  • 不想看到這個公司
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0~5人應徵

呃拍謝，搜尋結果好像很少

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4/29 【新加坡】美商資料儲存處理服務公司 誠徵 文件資料處理專員 (歷史悠久美商企業 ! 基本英文能力可應徵 ! 通過考核薪資將大幅調升 ! )

  • 新加坡
  • 2年以上
  • 大學

【關於我們】： 在過去70多年裡，我們一直是您的戰略合作夥伴。做為全球領先的訊息儲存管理服務商，我們受到全球超過225,000家企業的信任，其中包括95% 『財富美國1000強中』的企業。我們的核心理念是——不論它是什麼，無論它在哪裡，無論它以何種方式儲存，我們都將為其而存在。 我們是真正的合作夥伴關係，我們會為您完整保留企業知識、增強其運作效率、維護其安全性，並加速您的業務拓展的力量。我們創建了最先進而完整的作業模式，來彌補紙本文件、龐大數字、多方媒體資源資料和數據之間存在的物理差距，幫助建立起企業組織的韌性與穩固性，並承諾讓其能領您的企業朝向永續發展的方向前進。 -------------------------------------------------------------------------------------------- 【工作內容】 文件資料處理專員是負責在現場為客戶提供高效的掃描操作服務，需能在效率和花費成本中取得完美平衡。 • 提供出色的服務，與客戶建立良好的信任關係 • 能獨立為客戶提供一系列文件或影像處理服務 • 接收、分類、批次處理和準備文件並進行掃描建檔 • 謹慎移除所有裝訂物，避免造成紙張毀損，進而影響到文件儲存品質 • 將需要修復或進行電子化的文件資料進行掃描 • 操作並維護掃描設備 • 確保所有需掃描文件，其圖像完整清晰、文字內容完整且方向正確 • 對掃描文件、數據輸入和最終產出輸出進行詳細複查 • 根據需要將紙本文件整理至存檔箱中 • 確保所有日常運作功能正常，並報告美日作業情況 • 與團隊合作解決問題，提出優化方案，確保符合高水平的資料處理服務 • 執行其他管理層分配的職責 【上班時間】 1. 每日上午8:30~下午18:00，月休8天，一週工作5天，每週工作44小時，超過另計加班費 【薪資待遇】 1. 基本薪資: SGD2,100 2. 如有加班另計加班費 ※通過考核後薪資有望可達SGD 3,000，考核通過與所需考核時間接依個人表現與主管評定為主※ 【公司福利】 1. 過試用期後提供年假 7天 2. 提供有薪病假14天/ 住院有薪病假46天 3. 提供醫療補助及其他依照新加坡政府規定之保險 4. 如完成合約，提供免費一張回程機票 5. 提供年終獎金1個月 6. 公司提供制服

月薪49,350~70,500元 員工140人
11~30人應徵

4/29 【高薪76000起/期滿獎金2個月】新加坡華文幼教老師 (NTUC)

  • 新加坡
  • 經歷不拘
  • 專科

1.負責華文教學、教案撰寫 2.維護2-6歲孩童安全、需有愛心耐心 3.日常生活照顧、與家長建立良好關係 4.每周工作44小時，享有工作餐，每日工作8.5小時 5.月薪3250~3500新幣起(無經驗可)+期滿獎金2個月(約台幣15~17萬) 6.享有表現花紅(績效獎金1~2個月)及調薪升遷制度 7.特別彈性福利(150新幣/年) 8.年假14天/帶薪病假14天、醫療工商保險、公共假期11天/住院假一年60天 9.領取2年工作簽證，期滿可申請留用續簽 10.補助台北-新加坡經濟艙來回機票 11.歡迎幼保系在校生先面試~畢業後前往新加坡 加入遠誠LINE @ago4827c，問題諮詢專人回覆 諮詢信箱：[email protected]

月薪76,000~85,000元 員工400人
11~30人應徵

4/25 臨床專案管理師

  • 台北市內湖區
  • 經歷不拘
  • 碩士

【工作內容】: 1.企業與臨床及醫學研究合作與協助。 2.臨床前檢測及試驗的媒合與規劃。 3.各項產學合作規劃、諮詢。 4.各類型合作案之協調。 5.其他主管交辦事項 【薪資待遇】: 同國科會碩士或學士給薪標準，含勞健保及年終1.5個月

待遇面議
0~5人應徵

4/24 Patient Safety Specialist

  • 台北市信義區
  • 4年以上
  • 大學

Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or solicited from a clinical trial including safety database entry, AE review, write patient narratives with coding, follow-up of missing information, listedness assessment against appropriate label (For Marketed products, if applicable) Submission of expedited Serious Adverse Event (SAE) reports to clients, Regulatory Authorities, Ethics Committees, investigators, 3rd party vendors, Partners and Labcorp project personnel, if required & as agreed with client during study set-up, within study specified timelines Ensure all cases that require expediting reporting to worldwide Regulatory Agencies or other recipients are prioritised for processing and submission within the regulatory and/or study specific applicable timelines Prepares timely pharmacovigilance reports for products and safety issues, including Individual Case Summary Reports (ICSRs) of Serious Adverse Events (SAEs), Annual IND reports, European Annual Safety Reports (ASRs), Development Safety Update Report (DSUR), Periodic Reports (PRs) line listings, and aggregate reports Perform peer/independent QC of Safety reports as needed Work with Data Management or client on reconciliation of safety databases, if appropriate. Maintain a strong understanding of Labcorp’s safety database conventions or client-specific database conventions, as appropriate Maintains a comprehensive understanding of Labcorp PSS Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance. Assist in signal detection, trend and pattern recognition activities, as appropriate Monitor workflow for assigned studies/programs to ensure all the timelines are met. Assist in the development of departmental Work Instructions (WI) and Standard Operating Procedures (SOPs), as appropriate. Participate in the generation of monthly status and other project-specific reports ensuring the quality and accuracy of metrics/data provided. Support/train less experienced safety staff in all aspects of case-handling, adverse event reporting and other work, as needed. Begin to prepare Safety Management Plans (SMPs), Reconciliation Plans and other safety- specific plans under supervision. Responsible for making decisions regarding adverse event reporting within the guidelines of each specific project. Actively participates in project team and client meetings and liaise with clients, where appropriate; Assist with proactive quality issue resolution and implementation of actions, as needed Support audit or inspection preparations Assist in the review of cumulative safety data for submission to Drug Safety Monitoring Boards (DSMBs), regulatory authorities or clients Assist with the set-up of, and the provision of data to Safety Committees/DSMBs Build and maintain good PSS relationships across functional units. Demonstrate role-specific Competencies and company values on a consistent basis. Assist in the co-ordination of endpoint committees, as required Any other duties as assigned by management

待遇面議 員工99人 距捷運市政府站約260公尺
0~5人應徵

4/19 SMA(Site Management Associate)-ICON CORE TEAM

  • 台北市信義區
  • 1年以上
  • 大學

General Summary Provides overall support to study sites and clinical project teams engaged in clinical research studies. Adheres to applicable protocols, standard operating procedures (SOPs) and all applicable guidelines and regulatory requirements (e.g. ICH-Good Clinical Practice (GCP), Good Pharmacoepidemiology Practice (GPP), and country/region-specific regulations). Acts as primary point of contact for study sites. Primary Responsibilities • Assists in identifying study sites by performing site feasibility and recruitment tasks, e.g., completing, disseminating and reviewing responses to site recruitment questionnaires. • Completes essential document collection and review throughout the study lifecycle inclusive of site activation. Organizes and maintains site clinical trial master file (TMF) documents. • Sets up and maintains site-related data in applicable clinical systems according to procedures and guidelines. • Acts as primary site contact/liaison for study and site management issues including addressing questions, inclusive of protocol questions, managing study supplies and conducting offsite central monitoring visits/contacts (pre-study, initiation, monitoring and close out visits). Escalates issues and risks as needed. • Ensure timely and complete data entry by site. Perform data review inclusive of site level data review, query resolution, facilitate database closure and freezing procedures as per study plans. • Performs risk assessment and management responsibilities throughout the project including site process evaluation, addressing follow up items and issue escalation. • Performs all tasks in accordance with applicable guidelines, (e.g., ICH-GCP), company and sponsor SOPs, project plan, studyspecific processes, local regulatory requirements Requirements: • Bachelor’s degree or international equivalent • 1 year of relevant experience

待遇面議 外商公司 員工300人 距捷運台北101/世貿站約300公尺
0~5人應徵

4/24 新加坡駐店-婚紗主管/儲備主管

  • 新加坡
  • 6年以上
  • 大學

於台灣培訓後，長期駐點新加坡。 須有婚紗禮服單租公司相關管理經驗者5年以上 1.至少5年以上相關銷售及禮服經驗，目標導向。 2.顧客服務與管理，有高度服務理念與態度。 3.團隊精神者精神者，願意學習挑戰新事物。 4.對時尚流行有高度敏銳度。 5.門口接待相關經驗者。 6.外貌端莊、口齒清淅、具有業務相關者尤佳。 7.親和力高，認真負責。 銷售主管基本基礎： 1.指導員工並發展、管理與激勵並協助問題解決 2.門市銷售績效與目標管理，達成目標並持續提昇績效。 3.產品銷售及設計規劃、客戶服務等各方面均符合公司標準。 4.管理與維持門市環境與服務品質，提供客戶最佳消費體驗。 5.具高度服務熱忱，領導及教育員工。 6.良好的溝通能力與執行力 7.協助經營團隊執行公司決議事項及各項專案 *主動積極、抗壓性高、對婚禮有高度熱誠及品味

年薪1,500,000~2,000,000元 員工36人
0~5人應徵
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