Senior Regulatory Affairs & PV Specialist - Spain & LATAM

Pqe Group, a leader in the Pharmaceutical and Medical Device industries, is looking for a Senior Regulatory Affairs & Pharmacovigilance Specialist. This position requires expertise in EU and Spanish regulations and involves regulatory work along with pharmacovigilance oversight across Spain and LATAM markets.

The ideal candidate will have 4–5 years of experience in these fields and must be fluent in Spanish and English. Responsibilities include analyzing regulatory strategies, authoring technical dossiers, supporting regulatory activities, and ensuring compliance with safety regulations.