Pharma CSV Validation Lead
Listed on 2026-10-06
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Pharmaceutical
Regulatory Compliance Specialist, Pharma Engineer -
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Katalyst CRO is seeking a qualified professional with strong experience in pharmaceutical validation and CSVD lifecycle to lead and support validation activities. You will work with cross-functional teams to create, execute, and document validation deliverables in a regulated environment.
Candidates should have extensive knowledge of FDA/GxP guidelines, QA methodologies, and the ability to review tests, traceability, and design specs while coordinating with remote teams on multiple projects.
Are you ready to take on the Pharma CSV Validation Lead role at Katalyst CRO?
The Pharma CSV Validation Lead role at Katalyst CRO is now open for applications in Little Rock, AR, United States.
Join us at Katalyst CRO as our next Pharma CSV Validation Lead in Little Rock, AR, United States.
We are currently recruiting a Pharma CSV Validation Lead for our team in Little Rock, AR, United States.
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