Descripciรณn del Puesto
Are you ready to join a
world leader
in the exciting and dynamic fields of the
Pharmaceutical and Medical Device industries? We are currently seeking an
experienced
Commissioning, Qualification & Validation (CQV) Project Manager
in
Leรณn, Spain
. Lead and
execute commissioning, qualification, and validation activities
for
pharmaceutical/biotech equipment
and
systems
.
Prepare, review, and
execute C&Q and validation documentation
( URS, DQ, IQ, OQ, PQ protocols
,
test scripts
, and
summary reports ).
Collaborate
with
cross-functional teams
( Engineering, QA, Validation, Manufacturing ) to ensure
compliance
with
GMP
,
regulatory guidelines
, and
project timelines
.
Provide
project updates
and
progress reports
to
stakeholders
.
Bachelorโs degree
in
Engineering, Life Sciences
, or related field.
Ability to work
independently
and
collaboratively
in a
project environment
.
Fluent in
English
and
Spanish
( written and spoken ).
PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
Ready to Apply?
Don't miss this opportunity! Apply now and join our team.
Detalles del Puesto
Fecha de Publicaciรณn:
December 17, 2025
Tipo de Trabajo:
Negocios y Operaciones
Ubicaciรณn:
Spain
Company:
PQE Group
Ready to Apply?
Don't miss this opportunity! Apply now and join our team.