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, ...