
PLD Specialist (SH)

職位描述
職位職能:
??醫(yī)療器械注冊(cè)??
職位描述:
JOB TITLE: PLD Specialist (product labeling)
Location: Shanghai
1. PRIMARY PURPOSE AND OVERALL OBJECTIVE OF THE JOB
Process before SFDA registration submission, PLD is responsible to follow up with AS and Marketing on technical translation and validation to improve quality of labeling as well as to secure efficiency of registration key document preparation; Process after registration approval, PLD should upload approved labeling file to Live link to improve labeling updates; PLD takes a lead for labeling issue solution, and answer questions labeling related.
(1) Keep close eye to SFDA new regulation and notice for the change impact on labeling.
(2) Support RA registration for new, renew and modification on labeling
(3) Support PLD manager on labeling issue management.
(4) Maintain database to sure its accuracy and most updated.
(5) Internal Q&A for labeling concerns
(6) Participate in project planning activities, assessing necessary resources and estimating timelines for documentation development and production.
(7) Ensure consistency of processes and deliverables. To do so, write and format documentation according to established templates (provided by Corporate PLD) and departmental styles and standards. Proofread documentation for accuracy and adherence to departmental styles and standards.
(8) Compile reports, spreadsheets, and documentation as needed to support departmental workflow.
(9) Responsible for translation coordination and consolidating and reconciling all markups from internal reviewers during translation process. Schedule and facilitate technical review meetings. Regularly interface with cross-functional subject matter experts to ensure accuracy of deliverables.
(10) Track and implement change requests, errors, issues, and requirements logged against documentation.
(11) Define and manage final deliverables and surrounding processes, following appropriate change management processes.
2. KNOWLEDGE AND EXPERIENCE REQUIRED FOR THE JOB
Experience & Personality:
(1) 2 working experience in related field.
(2) Good communication
Education & Knowledge:
(1) Bachelor Degree or above in Biology, Microbiology, Medical related.
(2) Good writing
(3) Excellent in English
企業(yè)簡(jiǎn)介
生物梅里埃公司創(chuàng)建于1963年,公司依賴自身的科技研究和工業(yè)生產(chǎn)資源,始終致力于開(kāi)發(fā)作為醫(yī)療和工業(yè)用途的體外診斷產(chǎn)品。 集團(tuán)專(zhuān)門(mén)設(shè)計(jì)、開(kāi)發(fā)、生產(chǎn)和推廣應(yīng)用在臨床和工業(yè)的系統(tǒng)。生物梅里埃的診斷系統(tǒng)是由試劑、 儀器和軟件組成,主要是為傳染病、工業(yè)微生物控制、心血管病和腫瘤病等四個(gè)主要策略性領(lǐng)域來(lái)設(shè)計(jì)。
在2008年,公司銷(xiāo)售額為11億1千1百萬(wàn)歐元,集團(tuán)共有11個(gè)生產(chǎn)基地和9個(gè)研究中心,分布于歐洲、北美洲和南美洲。集團(tuán)全球擁有38個(gè)辦事處,至2008年12月31日集團(tuán)員工超過(guò)5,700人。
生物梅里埃公司產(chǎn)品有兩個(gè)應(yīng)用領(lǐng)域 : 臨床和工業(yè),臨床市場(chǎng)占總銷(xiāo)售額的85.5%,而工業(yè)市場(chǎng)占14.5%。工業(yè)的應(yīng)用主要在食品、藥品和化妝品的微生物分析,增長(zhǎng)非常迅速,生物梅里埃是全球體外診斷領(lǐng)域的第八大生產(chǎn)商。
生物梅里埃中國(guó)有限公司已經(jīng)20年的發(fā)展,自動(dòng)化微生物鑒定分析系統(tǒng)的用戶已達(dá)1400余家,自動(dòng)微生物培養(yǎng)系統(tǒng)已達(dá)700余家,全自動(dòng)細(xì)菌計(jì)數(shù)系統(tǒng)60余臺(tái),手工產(chǎn)品用戶覆蓋全國(guó)的省市70%以上。同時(shí)公司擁有數(shù)十名微生物臨床及工業(yè)領(lǐng)域?qū)I(yè)人員和工程技術(shù)人員,其中許多人員都來(lái)自檢驗(yàn)一線,擁有豐富的檢驗(yàn)經(jīng)驗(yàn)和儀器維修經(jīng)驗(yàn)。全面負(fù)責(zé)生物梅里埃公司產(chǎn)品的銷(xiāo)售,儀器的安裝、維護(hù)及保養(yǎng),以及用戶的培訓(xùn)及技術(shù)支持。
我們?yōu)閱T工提供具有競(jìng)爭(zhēng)力的福利待遇和培訓(xùn)機(jī)會(huì)。應(yīng)聘者請(qǐng)將中英文簡(jiǎn)歷和近照發(fā)至我司郵箱,注明應(yīng)聘職位。
職位發(fā)布企業(yè)
梅里埃診斷產(chǎn)品(上海)有限公司
企業(yè)性質(zhì):民營(yíng)企業(yè)
企業(yè)規(guī)模:100-499人
成立年份:1963
企業(yè)地址:中國(guó)(上海)自由貿(mào)易試驗(yàn)區(qū)富特西一路
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職位發(fā)布日期: 2015-07-21

