Company DescriptionWe suggest you enter details hereRole DescriptionThis 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.Qualifications- Proven experience in regulatory submissions and product registration in multiple international markets, especially in GCC/MENA and European countries .- Solid understanding of regulatory documentation, regulatory compliance, and registration requirements across different health authorities.- Excellent organizational and time management skills.- Strong collaboration abilities with cross-functional teams (e.G., R&D, Quality, Marketing).- Excellent written and verbal communication skills.- Bachelor's degree in Pharmacy, or a related field.- Familiarity with CTD/eCTD formats and international guidelines (e.G., ICH, EMA, SFDA, etc.) is a plus.