GMP QA Associate - Batch Release & Manufacturing Compliance

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

Benefits offered by this job

Health insurance

Job summary

Quality Chemical Laboratories (QCL) in Wilmington, NC, is seeking a Manufacturing Quality Assurance Associate with a scientific or engineering degree and GMP experience to perform GMP reviews and batch release.

The role includes reviewing deviations, SOPs, calibration records, protocols, and supporting client audits, with competitive compensation and growth potential within a rapidly expanding company.

Qualifications

• Bachelor's degree in a scientific or engineering field.
• 3+ years in GMP laboratory or GMP manufacturing.
• Experience reviewing manufacturing records, deviations, SOPs, calibration records, and protocols.

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

Record review

QA in pharma

Data review

GxP awareness

Education

Bachelor's degree in science or engineering

Tools

LIMS

Job description

Quality Chemical Laboratories (QCL) in Wilmington, NC, is seeking a Manufacturing Quality Assurance Associate with a scientific or engineering degree and GMP experience to perform GMP reviews and batch release.

The role includes reviewing deviations, SOPs, calibration records, protocols, and supporting client audits, with competitive compensation and growth potential within a rapidly expanding company.