Cognizant is seeking a CSV Validation Specialist to lead validation activities for pharmaceutical systems in GMP/GLP/GCP environments. You will craft validation plans, test protocols, URS/IQ/OQ/PQ, and traceability matrices while ensuring Regulatory compliance and quality management.
Experience with Lab systems and Ag ile practices is preferred. The role emphasizes documentation discipline, strong communication skills, and collaboration across QA, IT, and facilities teams within a US-based
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