CQV Packaging Equipment Specialist – GMP/FDA Validation
Listed on 2026-10-11
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Engineering
Quality Engineering, Pharma Engineer, Regulatory Compliance Specialist
Validation & Engineering Group, Inc. (a Pinnaql company) seeks a CQV Specialist - Packaging Equipment to support commissioning, qualification, and validation in a biotechnology manufacturing setting.
This on-site role in New Albany, OH focuses on package lines, labeling, serialization, and related systems, ensuring cGMP and FDA compliance throughout the validation lifecycle. You will develop and review IQ/OQ/PQ protocols, verify equipment readiness, and collaborate with engineering, quality,
This posting is for the CQV Packaging Equipment Specialist – GMP/FDA Validation role at Pinnaql, Inc., based in New Albany, OH, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the CQV Packaging Equipment Specialist – GMP/FDA Validation role in the description above.
We appreciate your interest in this position.
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