Specialist, Regulatory Affairs (Temporary Position)

Updated: April 24, 2024 05:15 PM GMT

Orifarm

Copenhagen

One of our employees has taken the opportunity to work at one of our production sites for the next year. We are therefore looking for a replacement until end of April 2025.

Do you want to become part of a dynamic organisation with many opportunities for personal and professional development? Do you enjoy combining your knowledge of chemistry and pharmaceutical science with regulatory work and do you have experience in lifecycle management? Then you might be the right match to the position as Regulatory Affairs Specialist in the Post Approval CMC team.

About The Job

As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.

Further, your main responsibilities include to:
• Gather information and documentation for... More Detail