Process Validation Specialist – Filling Operations

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.
Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación.
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.
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