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Experience: 5-10 yearsACSV Consultantis responsible for validating computerized systems used in regulated industries such as pharmaceuticals, biotechnology, healthcare, and medical devices to ensure compliance with regulatory requirements (FDA, GxP, 21 CFR Part 11).Key ResponsibilitiesPrepare and review validation documents (URS, FS, DS, IQ, OQ, PQ).Perform risk assessments and validation testing.Ensure compliance with FDA, GxP, and regulatory standards.Support audits, inspections, and quality a
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