Senior CQV Lead GMP Cell Therapy Validation
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Katalyst CRO seeks a Senior CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing.
The role requires owning qualification strategy and execution with a risk-based validation approach aligned to USP, GAMP 5, and industry best practices; you will drive deviations and investigations, author protocols/reports, and support inspection readiness.
Our organisation is growing, and we are hiring a Senior CQV Lead for GMP Cell Therapy Validation in Raritan, NJ, United States.
Learn more about the Senior CQV Lead for GMP Cell Therapy Validation role in the description above.
We appreciate your interest in this position.
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