We look for someone who excels at writing and explaining scientific facts. You will compile regulatory dossiers for our products for customers and / or Health Authorities worldwide.
This involves participation in development project teams, close cooperation with other departments and customers, and responding to Health Authority questions.
You will be solely responsible for various projects including maintenance of the regulatory dossiers, customer support, and review of GMP documents for compliance with regulatory dossiers and relevant guidelines.
We offer you a new challenge joining a motivated team in an internationally renowned company, and excellent terms and conditions.