? Implementation of quality control plan, preparation of test samples, test and analysis of test results;
質(zhì)量控制計劃的實施,檢測樣品的實驗準(zhǔn)備、檢測、檢測結(jié)果的分析;
? Drafting, sorting, archiving and maintenance management of testing records, reports, testing methods and other documents;
檢測記錄、報告、檢測方法等文件資料的起草、整理、存檔與維護(hù)管理;
? Ensure the necessary verification or validation of the required equipment;
保證所需儀器設(shè)備的經(jīng)過必要的驗證或確認(rèn);
? Responsible for equipment daily management, maintenance and troubleshooting;
負(fù)責(zé)儀器設(shè)備日常管理、維護(hù)及故障處理;
? Assist the pharmacovigilance department in relevant work, actively collect the adverse reaction information of the company's products, and immediately communicate with the PV department once the adverse reaction information is found or collected.
協(xié)助藥物警戒部門相關(guān)工作,主動收集公司產(chǎn)品不良反應(yīng)信息,一旦發(fā)現(xiàn)或收集到不良反應(yīng)信息,應(yīng)立即與PV部門溝通。
? Complete other tasks assigned by the superior.
完成上級交辦的其他工作。
任職要求
1、教育背景:本科及以上學(xué)歷;
2、專業(yè)要求:藥學(xué)、化學(xué)等相關(guān)專業(yè);
3、工作經(jīng)驗:3年以上同等崗位工作經(jīng)驗;
4、任職要求:具備藥品檢驗相關(guān)知識和基本操作