Senior Technical Writer – Regulatory (CMC)

Updated: April 23, 2024 12:32 PM GMT

Ferring Pharmaceuticals

Kastrup

Job Description:

Do you have deep insight into regulatory documentation on CMC development and manufacturing of pharmaceutical products? Are you looking to join an international environment with excellent development possibilities and opportunities to work with complex biological pharmaceuticals?
We are expanding our Technical Writing team and looking for an experienced colleague who wants to help set the company quality standard for our CMC documentation and contribute to the continuous development of our ways of working across development and technical operations.

Ferring + you You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.
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