Company:  Novo Nordisk Global Business Services (GBS)

Are you ready to shape how life-changing medicines reach patients across the globe? Join us as a Regulatory Professional II and play a pivotal role in driving timely submissions to Health Authorities worldwide, while strengthening Novo Nordisk's regulatory excellence across diverse markets.

Your new role
As a Regulatory Professional II, you will be responsible for making timely submissions to Health Authorities worldwide. You will establish and maintain the CMC part of the core regulatory file, while playing a key role in Life Cycle Management and stakeholder engagement across global and affiliate environments.

Your day-to-day responsibilities will include: