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 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. Participate in

Process Performance Qualification (PPQ)

activities and other validation lifecycle activities. Suppor...