Senior Regulatory Affairs & Pharmacovigilance Specialist

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.

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.

Key Responsibilities

Regulatory Affairs (RA)

• Analyze EU regulatory strategies and provide recommendations to clients
• Author full technical dossiers (Modules 1–5) from scratch
• Manage variations, renewals, labeling updates , and Health Authority ...