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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.
Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Manufacturing Quality Assurance Associate. This position, in the Manufacturing Quality Assurance department, requires a Bachelor’s degree or higher in a scientific or engineering discipline with either 3 years of experience or an equivalent combination of education and experience in a GMP laboratory or GMP manufacturing environment. Responsibilities include performing 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. QCL offers competitive salaries commensurate with experience and an excellent benefits package as well as great potential for career advancement and leadership in a rapidly growing company.
Quality Chemical Laboratories (QCL) serves the pharmaceutical industry.
We are an Equal Employment Opportunity (EEO) employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status or disability (in compliance with the Americans with Disabilities Act) with respect to employment opportunities.