Regulatory Writer

Updated: April 05, 2024 08:45 AM GMT

Ferring Pharmaceuticals

Kastrup

Job Description:

Do you have deep insight into regulatory affairs concerning the clinical and non-clinical aspects of drug development? Are you seeking an exciting job in an international company with excellent development possibilities and opportunities to work with innovative biological pharmaceuticals?

As our new regulatory writer, you will write and review high quality non-clinical and clinical documentation as well as help set the high quality standards for our documentation submitted to regulatory authorities.

Working on a range of pharmaceutical products across our therapeutic areas (reproductive and women’s health, gastroenterology, and urology), you will collaborate closely with the relevant regulatory colleagues in the therapeutic areas to drive and ensure timely readiness for regulatory submissions.

Ferring + you
This position is newly established within our Global Regulatory Affairs department, where you will become part of our Regulatory Writing team. We are... More Detail