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

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 include, but are not limited to: Execute and coordinate

process validation

and

cleaning validation

activities according to GMP requirements Draft, review, and approve validation documentation, including: Validation protocols, Risk assessments, Reports and SOPs and supporting document...