Cell Therapy CQV Engineer — GMP Validation Lead
Listed on 2026-10-07
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Pharmaceutical
Validation Engineer, Pharma Engineer, Regulatory Compliance Specialist
Katalyst CRO in New Jersey seeks a senior CQV professional to support commissioning, qualification and validation for our cell therapy manufacturing plant, ensuring compliant operations and data integrity. You will lead CQV protocols, summary reports, CAPAs and investigations, mentor junior staff, and coordinate with QA, manufacturing and regulatory teams for audits and product release.
Candidates should have 8+ years of CQV experience in aseptic cell therapy environments, with strong
The following opening is for a Cell Therapy CQV Engineer — GMP Validation Lead with Katalyst CRO.
We are seeking a motivated Cell Therapy CQV Engineer — GMP Validation Lead to join Katalyst CRO in Raritan, NJ, United States.
Consider building your career as a Cell Therapy CQV Engineer — GMP Validation Lead at Katalyst CRO.
The Cell Therapy CQV Engineer — GMP Validation Lead position in the Bio & Pharmacology & Health field is open for applications.
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