Leder i Storkøbenhavn
Would you like to be part of an area where we bring treatments to patients? Do you want to lead a skilled team and to set direction and pace of ambitious initiatives in the organisation? If you want to be part of a company with a high focus on work life balance, apply now for this life-changing career opportunity! You might be our new Associate Director in one of the Regulatory Affairs CMC & Devices departments in Søborg, Denmark.
The position
As an Associate Director in Regulatory Affairs CMC & Device, you will lead a dedicated team of experienced RA Professionals and play a pivotal role in shaping and influencing regulatory strategies and getting Novo Nordisk products to market.
Your main responsibilities will be focused on:
Qualifications
To be a competitive candidate, you should have: