Novo Nordisk A/S, Søborg
Novo Nordisk Regulatory Affairs (RAs) makes medicine available to patients all over the world by ensuring rapid regulatory approval in all of our markets. Regulatory Affairs is a fast-changing field, and the dedicated employees in our unit need both keen negotiating skills and scientific insight to serve as Novo Nordisk’s advocates around the world and make a meaningful difference to our business.
As a Regulatory Professional, you are responsible for planning, coordinating and submitting variation applications and to provide regulatory input in the cross functional projects you are involved in.
On a daily basis, you will support affiliate offices in responding to requests from authorities and reviewing the documentation needed for submission. You will review and assess change requests and non-conformities and play an important role in ensuring work processes are working smoothly and optimally.