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Cognizant is seeking a CSV Validation Specialist in Rahway, NJ to lead validation for pharmaceutical systems and equipment in GLP, GMP, and GCP environments. You will develop validation documents and work with QA, IT, and regulatory teams to ensure compliance.
Experience with FDA 21 CFR Part 11, EU Annex 11, and GAMP 5 is required. Strong writing and communication skills are essential, with a preference for Agile experience and tool familiarity such as Jira/Service Now.
*Please note this role is not able to offer visa transfer or sponsorship now or in the future*
We're excited to meet people who share our mission and who can make an impact in a variety of ways. Don't hesitate to apply—even if you only meet the minimum requirements. Think about your transferable experiences and unique skills that make you stand out.
Applications will be accepted until Sept 27, 2026,
The annual salary for this position is between $ 75,000 - $ 95,000 depending on experience and other qualifications of the successful candidate.
This position is also eligible for Cognizant’s discretionary annual incentive program, based on performance and subject to the terms of Cognizant’s applicable plans.
Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.