Cleaning Validation Specialist — GMP Compliance & QA Impact (Whitchurch-Stouffville)

Cleaning Validation Specialist — GMP Compliance & QA Impact (Whitchurch-Stouffville)

03 Oct
|
Teva Pharmaceuticals
|
Whitchurch-Stouffville

03 Oct

Teva Pharmaceuticals

Whitchurch-Stouffville

Teva Canada is seeking a detail-oriented Cleaning Validation Specialist for a 12-month contract in Stouffville, Ontario. You will support validation studies, coordinate sampling, and ensure GMP-compliant documentation across QA, QC, and Operations teams.

Requirements include a BSc/engineering field and 1–3 years in pharma/manufacturing, with solid data review, risk assessment, and regulatory knowledge. Travel to Teva sites may be required.

📌 Cleaning Validation Specialist — GMP Compliance & QA Impact (Whitchurch-Stouffville)
🏢 Teva Pharmaceuticals
📍 Whitchurch-Stouffville

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