GMP Manufacturing QA Associate — Batch Release & Audits
Listed on 2026-10-19
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Production QC/QA, Quality Control - QC Analysts/Managers
Quality Chemical Laboratories is seeking a Manufacturing Quality Assurance Associate in Wilmington, NC. The role supports GMP compliance, documentation control, and batch release in a growing pharmaceutical testing and manufacturing environment.
The candidate will review manufacturing records, deviations, SOPs, calibration records, and protocols, and assist during client audits. A Bachelor's degree in science or engineering with 3 years of GMP experience is required.
We are seeking a motivated GMP Manufacturing QA Associate — Batch Release & Audits to join Quality Chemical Laboratories in Wilmington, NC, United States.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Wilmington, NC, United States.
This opportunity is part of our work in Management & Operations, Engineering.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).