Description Overview

In this role you will be responsible for hands-on regulatory activities required for submission, approval, and launch of new products, as well as the maintenance of existing commercialized products in the Nordics (SE/DK/FI/NO/IS).

You will ensure that products across various categories (medicinal products, medical devices, food, food supplements, and cosmetics) comply with applicable regulatory requirements in the Nordic countries.

Another major aspect fo the rol will be to facilitate product introductions (launches) by enabling compliant product claims and removing regulatory barriers in the product listing process with customers.

Scope of the Role