(Senior) Specialist, Regulatory Affairs - Rare Disease
AstraZeneca View all jobs
- Beijing
- Permanent
- Full-time
- Implement regulatory strategies to achieve in-time and high quality approval and facilitate full speed launch.
- Maintain product licenses through timely lifecycle management with high standard.
- Effectively manage the local and global regulatory support systems/information to ensure good coordination for all stakeholders.
- Establish relationship with local regulatory authorities with the guidance of senior regulatory manager.
- Monitor local regulatory environments and communicate to key stakeholders, support to exert regulatory influence through company initiatives and/or industry association joint forces.
- Adherence to AZ and industry code of conduct, ethics and good regulatory practices including AZC RA SOPs and other required SOPs.
- Bachelor degree or above in Pharmacy, Medical, Biology or related field.
- have a proven track record from a leading pharmaceutical company.
- Understand the current regulatory practices and regulation in China.
- Strong collaboration across teams.
- Good project management skill.
- Fluent in both oral and written English.
- Good computer skill: word, excel, power point.
- Minimum 2 years’ experience in below position.
- Minimum 4 years working experience in regulatory affairs of MNC Pharma Company.