Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are seeking a Senior Regulatory Affairs & Pharmacovigilance Specialist to support both local and international regulatory and PV activities . The role combines hands-on regulatory work with pharmacovigilance oversight , ensuring compliance across Spain and LATAM markets.

Regulatory Affairs (RA):
Collaborate with global teams and international clients
Pharmacovigilance (PV):
Ensure compliance with local and international safety regulations
Coordinate with global PV teams to align processes and reporting

4–5 years of experience in Regulatory Affairs and/or Pharmacovigilance in pharma or consultancy




~ Strong knowledge of EU and Spanish regulations
~ Experience in general or corporate regulatory/PV environments
~ Fluency in Spanish and English (C1–C2); Nice-to-Have knowledge of Italian and/or Portuguese
~ Exposure to Medical Devices , Veterinary , Cosmetics , or Food Supplements
~ Strong interest in or experience with pharmacovigilance systems and processes
~ xbhjioe PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.

📌 Senior Regulatory Affairs (Barcelona)
🏢 Pqe Group
📍 Barcelona