Company Description
This is a full-time on-site role for a Regulatory Affairs Specialist located in Ávila. The Regulatory Affairs Specialist will be responsible for preparing, reviewing, and submitting regulatory documentation and dossiers. This role involves ensuring compliance with applicable regulatory requirements in various international markets, particularly in the MENA region (including the Gulf countries) and Europe.
Solid understanding of regulatory documentation, regulatory compliance, and registration requirements across different health authorities.
R&D, Quality, Marketing).
Bachelor’s degree in Pharmacy, or a related field.