Regulatory Affairs Specialist – Cmc (M/F/D)

Your new company

Join a pharmaceutical company in expansion as a Regulatory Affairs Specialist, supporting regulatory activities across international markets and contributing to a dynamic regulatory affairs team.

Your new role

This professional will be responsible for managing regulatory submissions and marketing authorizations, including variations, renewals, labelling updates and technical changes. Additionally, will develop regulatory strategies for CMC activities, assess regulatory impacts of product changes, support export market submissions and collaborate with cross-functional teams to ensure compliance with global regulatory requirements.

What you'll need to succeed

We are looking for a professional with a master’s degree in Pharmaceutical Sciences or similar, and at least 4 years of experience in Regulatory Affairs. Experience in CMC, labelling activities and...