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无工作经验 -
招1人 -
11-10 发布
职位描述
职位描述： Position Description？Compile registration dossier and prepare other regulatory documents, and make sure product registration to be finished timely and successfully.？Communicate internal and external on product registration issues.？Closely follow up product review process.？Properly maintain all regulatory documentation.？ Maintain close contact to regulatory authorities.？Assist in RA tasks/activities assigned？Position Requirements？Bachelor degree or above in Biochemistry, Biology or Medical examination.？1+ years relevant experience in medical device, or biologics industry.？Well know professional knowledge on regulatory affairs regulation: Chinese regulations, international guideline？Self-motivated with good communication skill and team spirit; willing to work under pressure.？Fluent English in verbal and written.？Good skills in standard PC software. 职能类别： 医疗器械注册
联系方式
北京市朝阳区太阳宫
公司信息
QIAGEN is the leading provider of sample and assay technologies. Sample technologies are used to isolate DNA, RNA and proteins from any biological sample. Assay technologies are then used to make specific target biomolecules, such as the DNA of a specific virus, visible for subsequent analysis. We have developed more than 500 consumable products and automated solutions. We are the market leader in academic research markets, to leading pharmaceutical and biotechnology companies, to molecular diagnostics laboratories as well as applied testing markets such as forensics, animal or food testing, and pharmaceutical process control. QIAGEN employs more than 3,900 people in over 35 locations worldwide. QIAGEN公司在全球35个国家，有着超过3900名员工和一支国际化的管理队伍。行业领先的技术使我们在未来能够持续成长和保持领先地位。 我们致力于全球生物技术市场。我们有着全球网络，代理商服务国家超过42个。同客户的紧密联系使得我们能够不断保持处于技术前沿，不断满足市场需求，不断完善我们产品发展系统。 从1986年以来，我们已经完善和上市了许多科研产品和工业的产品，应用于核酸纯化技术等方面，如：生命科学研究，基因组研究，基因药物发现，核酸分子诊断，基因疫苗和基因治疗市场等。核酸纯化市场的快速发展促使我们不断完善核酸纯化技术。
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