Lab Systems CSV Validation Engineer
Cognizant
Cognizant seeks a CSV Validation specialist with pharma domain expertise in Rahway, NJ. Responsibilities include developing validation documentation for GMP/GLP environments, creating URS, IQ/OQ/PQ, RTMs, and ensuring regulatory compliance across CS artefacts. Strong communication and technical writing skills are essential. The role emphasizes experience with FDA CFR 21 Part 11, EU Annex 11, GAMP 5, and SDLC; familiarity with lab systems, agile practices, and JIRA/ServiceNow is expected. #J-18808-Ljbffr Cognizant
Vacancy posted 2 days ago
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