Summary from listing
Nouryon is hiring a full-time Validation Specialist to qualify and validate pharmaceutical manufacturing, testing, storage, and distribution processes, equipment, computerized systems, facilities, and critical utilities in compliance with GMP and regulatory requirements. The role includes developing IQ/OQ/PQ protocols, coordinating validation activities, managing revalidations, supporting audits and quality documentation, and preparing validation reports. The position is permanent, based in Los Reyes, Mexico, and requires a bachelor’s degree in a relevant chemistry or chemical engineering field plus at least three years of pharmaceutical validation and GMP experience.
