Full-time Posted June 02, 2026
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Job Description

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 Cleaning Validation Specialist to support cleaning validation activities within a GMP-regulated pharmaceutical manufacturing environment.Responsibilities include, but are not limited to:Support the planning and execution of cleaning validation activities for manufacturing equipment and facilities.Assist in the preparation and review of validation protocols and reports.Participate in sampling activities and support analysis of validation data.Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure compliance with GMP requirements.Support risk assessments and validation strategies related to equipment cleaning processes.Contribute to investigations, deviations, and CAPA act...

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