Opportunity Description
Process Validation Specialist
Are you ready to join a world leader in the dynamic 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 across Europe, Asia, and the Americas.
Responsibilities
- Support the planning and execution of process validation activities related to aseptic 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.
- Contribute to investigations, deviations, and CAPA actions related to filling processes.
- Assist with risk a...
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