Regulatory Affairs Supervisor - Drug(职位编号:00081)
百特(中国)投资有限公司
- 公司规模:500-1000人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2013-09-04
- 工作地点:北京
- 招聘人数:若干
- 学历要求:本科
- 职位类别:药品注册
职位描述
Responsibilities:
Deliver the regulatory support on packaging materials and drug application including but not limited to:
Establish a thorough submission plan for each assignment within the timeline agreed by stakeholders.
Import renal drug registration.
Regulation Intelligence and Policy Analysis
Developing the working relationship with HA and its affiliates.
Requirements:
Bachelor degree or above in appropriate scientific discipline.
At least 5 years of experience in packaging materials or pharmaceutical industry.
Excellent knowledge and competency in Packaging materials & Drug registration.
Familiar with packaging materials and drug regulations and guidelines.
Good relationship with SFDA and affiliates, especially those Packaging materials and drug relevant.
Good communication skill, creative thinking, with teamwork spirit
Excellent spoken and written English skills.
Good Computer skill.
公司介绍
Baxter International Inc. provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; biosurgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s 50,000 employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.
联系方式
- Email:TTA@baxter.com
- 公司地址:杭州