Computer System Validation Specialist - GMP/CFRExpert
Listed on 2026-10-06
-
IT/Tech
IT QA Tester / Automation, Computer Science -
Quality Assurance - QA/QC
IT QA Tester / Automation
Quality Chemical Laboratories (QCL) in Wilmington, NC seeks a Computer System Validation Specialist to lead and execute validation activities in a GxP environment. Responsibilities include authoring validation plans, IQ/OQ/PQ, RTM, data integrity assessments and deviation management, with collaboration across functions.
Qualified candidates have at least 2 years in CSV, experience drafting test scripts, and knowledge of 21 CFR Part 11 and GAMP practices.
The Computer System Validation Specialist - GMP / 21
CFR
11 Expert position in the IT & Technology, Engineering field is open for applications.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Wilmington, NC, United States.
This opportunity is part of our work in IT & Technology, Engineering.
The advertised compensation is 85..
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