Teva Canada is seeking a detail-oriented Cleaning Validation Specialist to join our team in Stouffville, Ontario, on a 12-month contract. You will support cleaning validation activities to ensure cGMP compliance and collaborate across QA, QC, Operations, Engineering, and MS&T; to maintain validated processes. You will prepare protocols and reports, review data, and help with risk assessments and investigations while ensuring audit-ready documentation and adherence to regulatory standards.