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爱恩康临床医学研究(北京)有限公司诚聘Regulatory Affairs Specialist/药品注册专员人才,更多爱恩康临床医学研究(北京)有限公司Regulatory Affairs Specialist/药品注册专员招聘信息,请登录超级简历WonderCV查看详细的爱恩康临床医学研究(北京)有限公司对Regulatory Affairs
Regulatory Affairs Specialist 法规事务专员 1万-1.5万诗华诺康科技发展(北京)有限公司 北京 3-5年 本科 12-27 工作地址 诗华诺康科技发展(北京)有限公司职位描述 Position Responsibilities 岗位职责 1. Closely work with corporate and different campuses, responsible for dossier analysis and preparing regulatory ...
待解决 悬赏分:1 - 离问题结束还有 Regulatory Affairs Specialist问题补充:匿名 2013-05-23 12:21:38 法规事务专员 匿名 2013-05-23 12:23:18 监管事务专家 匿名 2013-05-23 12:24:58 管理事理专家 匿名 2013-05-23 12:26:38 监管事务专家 匿名 2013-05-23 12:28:18 管理事情专家 热门同步练...
To monitor the regulation updates and new registration cases in industry that LM Group involved. To prepare the annual cost budget for RA function. Working Partners/Contacts - Internal: International Registration Affairs team,Product Management, R&D, Technical Support of HQ, Product manager, Technical...
注册专员-Regulatory Affairs Specialist 1.5万-2万华辉安健(北京)生物科技有限公司 北京 3-5年 硕士 03-04 工作地址 中关村生命科学院医药科技中心5号楼职位描述 一、关键职责: 1、协助药品申报资料的撰写、整理和内部审核和及时递交; 2、协助注册项目的统筹、协调、实施及执行,跟踪项目研发及注册申报进度,协助...
Regulatory Affairs Specialist10-20k 上海5-10年统招本科 五险一金绩效奖金带薪年假节日礼物交通补助领导好公司规模大发展空间大管理规范岗位晋升 浏览更多优质职位 浏览原职位详情 登录
Regulatory Affairs Specialist | Process Improvement | IVD Knowledge +1-(234)-555-1234 help@enhancv.com linkedin.com San Diego, California Summary With over 7 years of regulatory experience in the medical device industry, my expertise spans across compliant market entry, efficient process management,...
2525 McGaw Avenue P.O.Box 19791 Irvine, CA 92623-9791 Attention: DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration Rockville, MD 20857 Pushpa Mehta, RAC Regulatory Affairs Specialist Dear Ms. Mehta: Please refer to your supplemental new drug application ...
职位描述 Mozarc 血透 有源注册 Role Summary/Purpose: Ensure the company’s regulatory affairs activities are conducted accurately, ethically based upon relevant regulations and standards, develop and execute RA registration plan, and ensure rapid and timely approval of products. ...