Onsite Pharma Validation Engineer - GMP/CSV Expert
Listed on 2026-10-13
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Pharmaceutical
Pharma Engineer, Quality Engineering, Regulatory Compliance Specialist
Piper Companies seeks a Validation Engineer for a long-term onsite contract in Clayton, NC, to support validation work across manufacturing, facilities, lab, automation, and quality systems while maintaining GMP/FDA compliance.
Ideal candidate brings 5+ years in pharma validation, hands-on IQ/OQ/PQ, and experience with SCADA, PLCs, PAS-X, LMES, Veeva, and HP ALM/TIMS in regulated settings.
Step into the Onsite Pharma Validation Engineer - GMP/CSV Expert role at Piper Companies in Clayton, NC, United States and grow with us.
The Onsite Pharma Validation Engineer - GMP/CSV Expert role at Piper Companies is now open for applications in Clayton, NC, United States.
Join us at Piper Companies as our next Onsite Pharma Validation Engineer - GMP/CSV Expert in Clayton, NC, United States.
We are currently recruiting a Onsite Pharma Validation Engineer - GMP/CSV Expert for our team in Clayton, NC, United States.
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