Senior QA oversight specialist for pharmaceutical computerized systems and data integrity.
Deliver independent quality assurance and documented challenge of operational technology CSV systems and data-integrity remediation in a regulated pharmaceutical environment. Review validation strategies, risk assessments, and GMP compliance evidence; verify controls and electronic-record lifecycle management with specialists; and make acceptance/rejection recommendations. Requires 10+ years of direct FDA inspection experience on computerized systems, deep expertise in regulatory frameworks (Part 11, Annex 11, GAMP 5), and preferably hands-on knowledge of DeltaV automation platforms.
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Found at a specialist agency · listed 21 October 2026 · InsideJobs links you to the original posting.