CQV Validation Lead: GMP Documentation Audit
Listed on 2026-10-07
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Quality Engineering -
Pharmaceutical
Regulatory Compliance Specialist, Pharma Engineer, Quality Engineering
FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a major pharmaceutical facility construction project in Durham, NC. You will establish standardized validation processes for hygienic welding documentation (Isometrics) to ensure traceability and compliance with FDA cGMP, GDP, and project specifications.
The role requires 8+ years in pharmaceutical validation and CQV, with proven leadership of large teams, strong project management, and
The CQV Validation Lead: GMP Documentation Audit role at FST Technical Services is now open for applications in Durham, NC, United States.
We invite applications for the CQV Validation Lead: GMP Documentation Audit position located in Durham, NC, United States.
The following opening is for a CQV Validation Lead: GMP Documentation Audit with FST Technical Services.
Our group is growing, and we are hiring a CQV Validation Lead: GMP Documentation Audit in Durham, NC, United States.
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