GMP Quality Assurance Associate – Batch Release & Compliance

The Charlotte Observer Publishing Company; Wilmington (NC); Hybrid; USD 65,000 - 85,000; Full time

Job summary

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.

Qualifications

• Bachelor’s degree or higher in a scientific or engineering discipline with 3 years of GMP experience or an equivalent combination of education and experience in a GMP laboratory or GMP manufacturing environment.

Responsibilities

• Perform 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 and assist with client audits.

Skills

GMP experience

Quality assurance

Document review

Education

Bachelor’s degree or higher in a scientific or engineering discipline

Job description

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.