PLD Specialist (SH)
职位描述
职位职能:
??医疗器械注册??
职位描述:
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
企业简介
生物梅里埃公司创建于1963年,公司依赖自身的科技研究和工业生产资源,始终致力于开发作为医疗和工业用途的体外诊断产品。 集团专门设计、开发、生产和推广应用在临床和工业的系统。生物梅里埃的诊断系统是由试剂、 仪器和软件组成,主要是为传染病、工业微生物控制、心血管病和肿瘤病等四个主要策略性领域来设计。
在2008年,公司销售额为11亿1千1百万欧元,集团共有11个生产基地和9个研究中心,分布于欧洲、北美洲和南美洲。集团全球拥有38个办事处,至2008年12月31日集团员工超过5,700人。
生物梅里埃公司产品有两个应用领域 : 临床和工业,临床市场占总销售额的85.5%,而工业市场占14.5%。工业的应用主要在食品、药品和化妆品的微生物分析,增长非常迅速,生物梅里埃是全球体外诊断领域的第八大生产商。
生物梅里埃中国有限公司已经20年的发展,自动化微生物鉴定分析系统的用户已达1400余家,自动微生物培养系统已达700余家,全自动细菌计数系统60余台,手工产品用户覆盖全国的省市70%以上。同时公司拥有数十名微生物临床及工业领域专业人员和工程技术人员,其中许多人员都来自检验一线,拥有丰富的检验经验和仪器维修经验。全面负责生物梅里埃公司产品的销售,仪器的安装、维护及保养,以及用户的培训及技术支持。
我们为员工提供具有竞争力的福利待遇和培训机会。应聘者请将中英文简历和近照发至我司邮箱,注明应聘职位。
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职位发布日期: 2015-07-21