Position

Director, Regulatory Affairs

Job description

Job description

Location

Beijing, China Mainland

Job category

Reg Affairs & Safety Pharmacovigilance

   

Key responsibilities 重要职责

 

  1. Regulatory strategy development and execution for drug shortage
  2. Regulatory Planning and Development Strategy
  3. Submissions and Approvals for New Products
  4. Product Life Cycle Management
  5. Management and people development
  6. Cross Functions/Departments Supporting
  7. Regulatory Influence
  8. Budget Planning and Control

 

Education 教育背景

 

  • Bachelor degree of pharmacy, life science or advanced degree
  • Fluency in both written & spoken English

 

Experience 经验

 

  • 10+ years of regulatory affairs experience
  • At least 5 years people management.
  • Excellent regulatory related knowledge (regulations, guidelines, RA intelligence) and experience in multi-therapeutic areas

 

Personal skills 技能

 

  • Strong leadership with team spirit
  • Strong negotiation capacity and communication skill

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.