南京招聘

Regulatory Affairs Assistant Manager

Position Summary: The Regulatory Affairs Assistant Manager will be a part of a very professional and dedicate global regulatory group placed in Denmark, US, Hungary, Japan, India, Croatia and China. You will be working from the Xellia office in Shanghai.

Recruiting Qualification for RA Assistant Manager

• Min. a bachelor degree in Chemistry, Pharmacy, or any other relevant natural science area

• Min. 3 years of experience within China API registration and life cycle management activities for API – preferable fermentation based APIs

• Knowledge about China FDF registration and life cycle management is preferred

• Very good English communication skills– written as well as oral

• Experience working in multi-cultural teams is preferable

药政法规事务助理经理

药政法规事务助理经理，你将成为Xellia分布于丹麦、美国、匈牙利、日本、印度、克罗地亚和中国的专业团队的一员。你将在Xellia上海代表处工作。

药政法规事务助理经理 的招聘条件

1. 药学，化学或其它相关自然科学学科的本科及以上学历

2. 至少有3年原料药在国内的注册经验和生命周期管理经验，有发酵原料药经验优先

3. 了解中国FDF注册和生命周期管理者优先

4. 熟练的英文书写能力和口语技巧

5. 有多元化团队工作经验者优先

Xellia制药隶属于诺和集团，是一个致力于在抗感染治疗领域研发、生产和销售的专业制药公司。总部位于丹麦的歌本哈根。全球的工厂位于欧洲、北美洲和亚洲。目前有员工1700多人。对于开发针对感染疾病的最终治疗，公司具备100多年的行业经验。 Xellia专注于挽救生命，同时也专注于提高病人的生活质量。
Xellia Pharmaceuticals, owned by Novo Holding A/S, is a specialty pharmaceutical company leading in the development, manufacture and supply of anti-infective treatments. Headquartered in Copenhagen, Denmark, Xellia has global facilities in Europe, North America, and Asia, currently employing over 1700 people. With over 100 years of industry experience in developing last resort treatments for infectious diseases, Xellia is focused on the supply of products which not only save lives, but also improve and enhance patients’ quality of life. Together with us, you can help lead the fight against bacterial infections.