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 collection and analysis during validation runs and routine manufacturing.Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure GMP compliance.C...