Global CQV Quality Lead - Travel, GMP Readiness
Listed on 2026-10-28
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Engineering, Regulatory Compliance Specialist
Telix Pharmaceuticals is seeking a CQV Lead responsible for quality assurance oversight across the Telix Manufacturing Solution network in the United States. The role requires extensive travel and collaboration with Engineering, Validation, Manufacturing, Quality Control, IT, and Regulatory Affairs to ensure GMP readiness and site activation.
You will review validation lifecycle documents, manage deviations and CAPAs, and drive operational readiness from project execution to routine GMP
The Global CQV Quality Lead - 75% Travel, GMP Readiness position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
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