长沙招聘

Job Description:

- Be fully responsible for the registration of assigned projects;
- Contribute to registration timeline, prepare documentation and submission on schedule;
- Follow up the registration and evaluation status in SFDA & CDE;
- Answer technical questions from SFDA & CDE;
- Be responsible for the sample order, dossier order;
- Be responsible for dealing with relative issue on drug quality test in SDA's lab;
- Effectively and clearly communicate with external functions and other internal line functions;
- Provide technical and regulatory advice for the new product together with BD colleagues.

Education and Experience Requirements of the Position:

- Over 2 years registration experience;
- Good project management and problem solving skill with team work spirit;
- Be familiar with regulation requirements;
- Good communication skill in both English and Chinese.
- Bachelor or above
- Pharmaceutical education background prefer

捷斯瑞医药有限公司（www.gc-rise.com）是一家由欧洲知名的专注于健康产业的投资公司Inventages在华投资的外商独资企业。公司秉承“致力人类健康，创造美好生活”的使命，充分利用我们在美国、欧洲和日本战略合作伙伴的业务发展网络以及在中国丰富的临床开发、试验、注册的经验，雄厚的商业分销、医院销售和市场营销的实力，为中国广大的患者带来新型、安全、高效的医疗产品和治疗理念。
公司强调以人为本，重视人员的培养和发展。竭力为员工提供广阔的发展空间，实现公司与员工共同发展的最终目的。捷斯瑞将始终为各类人才打造一个施展才华的平台，并努力为求职者的职业生涯提供一个愉快、健康向上的工作环境。
满足公司价值观“以人为本，诚信正直，追求卓越，勇于负责，持之以恒，沟通团结，积极热情，变革创新，快速反应”的应聘者将是我们的首选对象。
应聘简历请发送至公司邮箱。
非常感谢您向我公司提交简历，对于合格的应聘者，我们会发送面试通知。更多详细情况请登陆：捷斯瑞医药有限公司网站http://www.gc-rise.com