Major responsibilities/主要職責(zé): -Keep contact with inspection institute, complete homologation sample inspection work independently 保持和檢測全部效交流, 自立完成樣品檢測工作 -Be proficient in communication with provincial and city FDA, handle problem on market surveillance actively 擅長和各地藥監(jiān)局交流,樂觀處理市場監(jiān)管中發(fā)覺的問題 -Internal quality consciousness and knowledge training 企業(yè)內(nèi)部質(zhì)量意識和學(xué)問培訓(xùn) -Co-work with other departments, improve quality system and solve the related problem issue. 跨部門配合,推動質(zhì)量改進, 解決相關(guān)質(zhì)量問題 -Technical document translation (English) 技術(shù)文檔翻譯(英語) -Handle/ archive quality related documents and record 處理并管理質(zhì)量相關(guān)文檔和記錄 -Complete other tasks from manager 完成上級布置的其他任務(wù) Requirements/資歷要求: -Medical device, biomedical engineering, mechanical engineering, electronic engineering, bioengineering, Chemical, Ecsomatics and so on. Associate degree and above. 醫(yī)療器械、生物醫(yī)學(xué)工程、機械、電子、生物工程、化學(xué)、檢驗學(xué)、等專業(yè),大專及以上 -At least two years relevant work experience,prefer medical device industry experience 2年以上相關(guān)工作閱歷,有醫(yī)療器械企業(yè)相關(guān)工作閱歷更佳 -Be familiar with China medical device inspection standard and related regulation 認識中國醫(yī)療器械檢測標(biāo)準和相關(guān)規(guī)矩 -Skilled use of office software 嫻熟使用office辦公軟件 -Fluent English ( reading and writing ) 英語讀寫流利