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 integral 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 global 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 ~ 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 (Cataluña)
🏢 Pqe Group
📍 Cataluña