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 eCTD submissions is essential. Fluency in English is required, while French will be considered an advantage. Strong organizational, communication and stakeholder management skills are highly valued.

What you'll get in return

An excellent opportunity to join a pharmaceutical company in expansion offering attractive benefits, ongoing professional development and a collaborative and supportive work environment.

What you need to know

If you're interested in this role, click apply now to submit your CV. If this position isn’t the right fit but you're exploring new opportunities, contact us for a confidential career discussion.