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.
• Support data colle...