IT Validation Specialist – 2-Year Onsite Contract (Greater Raleigh area)
What You’ll Do:
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Plan, develop, and execute IT validation and compliance activities (CSV, protocols, test plans, reports).
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Manage validation/change control documentation and decommissioning activities.
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Investigate validation deviations and implement corrective actions.
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Ensure compliance with 21 CFR Part 11, SOX, GxP, and internal SOPs.
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Support system lifecycle activities — maintenance, incident/change management, risk assessment, and data integrity.
What We’re Looking For:
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5+ years of experience in computer system validation (CSV).
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Pharmaceutical IT project experience required.
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Strong understanding of GxP, validation deliverables, and audit readiness.
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BS in Engineering, Computer Science, or related field preferred.
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Knowledge of Fill/Finish manufacturing processes a plus.
If you have solid CSV experience in the pharma space and enjoy hands-on work in a collaborative, compliant environment, we’d love to connect!
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