Grifols, S.A. seeks an experienced QA Auditor to plan and conduct audits of CROs, vendors, and investigator sites, ensuring compliance with applicable regulations and standards.
The role also conducts internal GCP process audits and reviews procedures for clinical audits, providing guidance to clinical staff on resolving findings. The candidate should have a PhD or Master in pharmaceuticals or life sciences, 2–3 years of GCP/GCLP QA experience, advanced English, and travel availability.
📌 Global Clinical QA Auditor (San Cugat del Vallés)
🏢 Grifols
📍 San Cugat del Vallés
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