Grifols is seeking an R&D; QA Specialist & Auditor to provide quality oversight of SIO pre-clinical activities, ensuring studies, systems and documents meet regulatory requirements and company standards.The role requires 2-5 years in pharma QA or similar GLP environment, with strong GCLP/GMP/GLP knowledge and advanced English. Hybrid work in Sant Cugat del Vallès offers diverse, impactful projects in a integral healthcare leader.
📌 Auditor de QA preclínico (Barcelona)
🏢 Capgemini Engineering
📍 Barcelona
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