職位描述
職位類別:醫(yī)療 | 制藥 | 環(huán)保/制藥/生物工程/生物工程/生物制藥
Major responsibilities/主要職責(zé):
-Keep contact with inspection institute, complete homologation sample inspection work independently
保持和檢測(cè)全部效交流, 自立完成樣品檢測(cè)工作
-Be proficient in communication with provincial and city FDA, handle problem on market surveillance actively
擅長(zhǎng)和各地藥監(jiān)局交流,樂觀處理市場(chǎng)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(shí)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(dòng)質(zhì)量改進(jìn), 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(jí)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(jī)械、電子、生物工程、化學(xué)、檢驗(yàn)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(rèn)識(shí)中國(guó)醫(yī)療器械檢測(cè)標(biāo)準(zhǔn)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