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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 looking for a
Process Validation Specialist
to support validation activities related to
aseptic filling operations
within a GMP-regulated pharmaceutical manufacturing environment.
Responsibilities include, but are not limited to:
Support the
planning and execution of process validation activities
related to filling operations.
Assist in the preparation and review of
validation documentation, including protocols and reports.
Participat...