07 sep
|
Pqe Group
|
Barcelona
07 sep
Pqe Group
Barcelona
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 interactions
Support
regulatory activities in LATAM markets
Collaborate with
global teams
and
international clients
Pharmacovigilance (PV):
Support
PV activities
and
reporting obligations
in
Spain
and
EU
Ensure compliance with
local and international safety regulations
Assist in
signal detection ,
risk management , and
safety documentation
Coordinate with
general PV teams
to align
processes
and
reporting
Requirements
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
Experience with
LATAM regulatory/PV activities
Exposure to
Medical Devices ,
Veterinary ,
Cosmetics , or
Food Supplements
Strong interest in or experience with
pharmacovigilance systems
and
processes
Salary starting from
€35,000 gross per year
Next Steps
Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive m
📌 Senior Regulatory Affairs (Barcelona)
🏢 Pqe Group
📍 Barcelona