Nouryon is seeking a Validation Specialist to join our Los Reyes, MX team. You will ensure that manufacturing processes, equipment, and systems are properly qualified and validated in line with GMP and regulatory requirements.
Reporting to the GMP Quality Specialist, you will develop IQ/OQ/PQ protocols, coordinate validation activities, manage revalidations, and support audits. A chemical engineering or pharmaceutical chemistry degree with at least 3 years of pharma validation experience is
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📌 Pharma Validation Specialist: GMP & Compliance (Puerto El Pino)
🏢 Nouryon
📍 Puerto El Pino
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