超碰免费人人成人色综合|日韩精品免费一区二区三区夜夜嗨|久久av电影av色v|精品水牛三区黄色片流行|亚洲最大成人免费激情片|超碰欧美日韩国产熟女在线|av一级黄色毛片|日本一道二道高清视频在线免费看|色一色成人网亚洲色伦|日本黄色网有哪些

工作職責:
84 負責實驗室信息化項目的整個生命周期，包括需求分析、規(guī)劃、實施、測試、發(fā)布和維護，滿足實驗人員在項目管理、實驗記錄、資源管理、數(shù)據(jù)可視化方面的需求；
84 負責實驗室信息化系統(tǒng)的質(zhì)量管理，實現(xiàn)信息化系統(tǒng)全生命周期的質(zhì)量保障，并滿足計算機化系統(tǒng)驗證管理要求；
84 以系統(tǒng)質(zhì)量管理角色參與系統(tǒng)的運維階段活動，保障系統(tǒng)運維過程中各項活動，如變更、事件、偏差等，符合質(zhì)量管理的要求；
84 負責客戶或機構對項目相關信息化系統(tǒng)的審計工作；
84 負責產(chǎn)品的更新管理，熟悉軟件項目管理、軟件測試與部署相關過程；
84 負責自定義功能的自主源碼開發(fā)或使用低代碼平臺進行應用開發(fā)。
84 Responsible for the entire lifecycle of laboratory informationization projects, including requirement analysis, planning, implementation, testing, release, and maintenance, to meet the needs of laboratory personnel in project management, experiment recording, resource management, and data visualization
84 Responsible for the quality management of laboratory information systems, ensuring the quality assurance of the entire lifecycle of information systems, and meeting the requirements of computerized system verification management
84 Participate in the operation and maintenance activities of the system as a system quality management role, ensuring that all activities during the system operation and maintenance process, such as changes, events, deviations, etc., meet the requirements of quality management
84 Responsible for auditing project related information systems by clients or institutions
84 Responsible for product update management, familiar with software project management, software testing, and deployment related processes
84 Responsible for independent source code development of custom features or application development using low code platforms
任職資格:
84 本科或以上學歷，計算機相關專業(yè)或藥物相關專業(yè)或數(shù)學相關專業(yè)；
84 3年及以上信息化產(chǎn)品管理經(jīng)驗或信息化團隊管理經(jīng)驗；
84 1年及以上藥物研發(fā)行業(yè)信息化系統(tǒng)驗證經(jīng)驗；
84 掌握至少一門編程語言，如python, Java；
84 熟練使用AI編程工具；
84 優(yōu)秀的團隊溝通和人際溝通能力，善于跨部門協(xié)調(diào)。
84 Bachelor's degree or above, major in computer related, pharmaceutical related, or mathematical related fields
84 3 years or more of experience in information product management or information team management
84 At least 1 year of experience in validating information systems in the pharmaceutical research and development industry
84 Master at least one programming language, such as Python, Java
84 Proficient in using AI programming tools
84 Excellent team communication and interpersonal skills, adept at cross departmental coordination