Experteer Italy seeks a CQV Engineer to develop and execute commissioning, qualification, and validation documentation for pharmaceutical facilities and equipment in Italy. You’ll lead protocol writing, field verifications, and summary reports at client sites, supporting FATs, SATs, IOQ and PQ executions throughout the lifecycle. xysqume
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Ideal candidates have 2–3 years in FDA‑regulated CQV, strong problem solving, and excellent English.
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📌 CQV Engineer: Life Sciences Validation Lead (Milano)
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📍 Milano