Pharma Validation Engineer; GMP/CSV, Onsite
Listed on 2026-10-20
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Pharmaceutical
Pharma Engineer, Quality Engineering, Pharmaceutical Manufacturing, Regulatory Compliance Specialist
Piper Companies seeks a Validation Engineer for a long-term onsite contract in Clayton, NC. The role spans manufacturing, facilities, laboratory, automation, and quality systems, ensuring GMP and FDA compliance.
Candidates should bring 5+ years of pharma validation, IQ/OQ/PQ experience, and a Bachelor’s degree in a related field. Compensation ranges $71-$81/hr with comprehensive benefits.
Step into the Pharma Validation Engineer (GMP/CSV, Onsite) role at Piper Companies in Clayton, NC, United States and grow with us.
We invite applications for the Pharma Validation Engineer (GMP/CSV, Onsite) position located in Clayton, NC, United States.
The following opening is for a Pharma Validation Engineer (GMP/CSV, Onsite) with Piper Companies.
Our group is growing, and we are hiring a Pharma Validation Engineer (GMP/CSV, Onsite) in Clayton, NC, United States.
This opening is for the Pharma Validation Engineer (GMP/CSV, Onsite) role at Piper Companies.
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