Quality Audit Lead: GMP Compliance & Inspections
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Experis Technology Group's client in the pharmaceutical/medical device sector seeks a Quality Specialist III for Greenville, NC to support audits, inspections, and quality systems. You will execute internal audits, support regulator inspections, and drive data-driven improvements.
The role requires strong knowledge of FDA regulations and QMS (Documentum, Veeva Vault, Track Wise) plus cross-functional collaboration across teams.
The Quality Audit Lead: GMP Compliance & Inspections role at Experis Technology Group is now open for applications in Greenville, NC, United States.
We have an opening for a Quality Audit Lead: GMP Compliance & Inspections in Greenville, NC, United States within Legal, Management & Operations.
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