Senior Pharmaceutical Affairs Consultant

This key role supports AzurBio Pharma’s “Exploitant” activities in France, ensuring compliance with regulatory requirements while facilitating market entry for innovative biopharmaceutical companies.

 

It emphasizes a strong focus on scientific and regulatory affairs, quality management, and risk mitigation to uphold the highest operational standards.


By contributing to strategic partnerships, this role helps bring life-changing treatments to patients across Europe.

Looking to enter the EU market?
Contact us today.