GMP Quality Assurance Associate – Batch Release & Compliance
Listed on 2026-10-18
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Quality Chemical Laboratories (QCL) in Wilmington, NC, a leading pharmaceutical testing and manufacturing laboratory, seeks a Manufacturing Quality Assurance Associate. A Bachelor’s degree or higher in a scientific or engineering discipline with 3 years of GMP experience (or an equivalent combination) is required.
Responsibilities include reviewing GMP manufacturing records and data, releasing batches, approving deviations, SOPs, calibration records, and protocols.
We would love to welcome a new GMP Quality Assurance Associate – Batch Release & Compliance to our group in Wilmington, NC, United States.
The GMP Quality Assurance Associate – Batch Release & Compliance position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
We have an opening for a GMP Quality Assurance Associate – Batch Release & Compliance in Wilmington, NC, United States within Bio & Pharmacology & Health, Management & Operations.
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