Senior Regulatory Affairs & Pharmacovigilance Specialist

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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...