GMP Manufacturing QA Associate — Batch Release & Audits

Quality Chemical Laboratories; Wilmington (NC); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Excellent benefits package

Job summary

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.

Qualifications

• 3 years of experience in GMP laboratory or GMP manufacturing environment.
• Bachelor's degree or higher in a scientific or engineering discipline.
• Strong attention to detail and documentation skills.

Responsibilities

• GMP review of manufacturing records and data.
• Review and release manufacturing product batches.
• Review and approve deviations, SOPs, calibration records, and protocols.
• Perform AQLs as required.
• Assist with client audits.

Skills

GMP experience

Quality assurance

Documentation review

Data review

Attention to detail

Education

Bachelor's degree in science or engineering

Job description

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.