Pharma CQV Validation Lead
Listed on 2026-10-11
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Pharmaceutical
Pharma Engineer, Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Quality Engineering -
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Synerfac Inc. is seeking a Validation Specialist for a multi-year project portfolio at its Clayton, NC site.
The contract role (24 months, with potential extension) will lead validation across several projects, aligned to expertise in aseptic filling, device assembly and packaging, automation, facility systems, warehouse, and QC. The role requires 5+ years CQV experience, hands-on validation documentation, and strong GMP/FDA knowledge.
The Pharma CQV Validation Lead – 24-Month Contract role at Synerfac Inc is now open for applications in Morrisville, NC, United States.
Join us at Synerfac Inc as our next Pharma CQV Validation Lead – 24-Month Contract in Morrisville, NC, United States.
We are currently recruiting a Pharma CQV Validation Lead – 24-Month Contract for our team in Morrisville, NC, United States.
This is a strong opportunity to take on the Pharma CQV Validation Lead – 24-Month Contract role at Synerfac Inc.
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