Experteer Italy is seeking a Global R&D; QA Specialist to lead validation of computerized systems in GXP environments, ensuring controlled state and compliance with regulatory expectations. You will collaborate across R&D; functions to align CSV activities with regulatory expectations and continuous improvement.
The role requires at least 5 years of CSV experience in the pharmaceutical industry, excellent knowledge of CFR 21 Part 11 and EU GMP Annex 11, and strong Data Integrity and risk
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📌 Global R&D QA Lead: CSV & Data Integrity (Parma)
🏢 Experteer Italy
📍 Parma
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