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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
Process & Cleaning Validation Specialist
with solid experience in pharmaceutical validation activities. The consultants will be involved in validation lifecycle management, supporting both routine and project‑related activities in a GMP‑regulated environment.
Responsibilities
Execute and coordinate
process validation
and
cleaning validation
activities according to GMP requirements
Draft, review, and approve validation documentation, including: Validation protocols, Risk assessments, ...