We are seeking a QA Specialist with GMP experience to provide basic quality support for a pharmaceutical manufacturing environment. This role will support day-to-day quality assurance activities, with a strong focus on deviation management and GMP documentation. The ideal candidate will have experience working in a regulated pharmaceutical setting and be comfortable supporting investigations and quality systems.
This position is on-site in Smyrna, GA and is a one-year contract role supporting quality operations.
Provide Quality Assurance support for manufacturing and quality systems in a GMP-regulated pharmaceutical environment.
Review and assist with deviation investigations, ensuring timely documentation and closure.
Support GMP documentation review, including batch records, SOPs, and quality records.
Assist in root cause analysis and corrective/preventive actions (CAPA) related to deviations.
Ensure compliance with GMP regulations and internal quality standards.
Collaborate with manufacturing, quality control, and regulatory teams to resolve quality issues.
Maintain accurate documentation and support inspection readiness.
Participate in quality meetings and provide basic QA support across quality systems.
Required
Bachelor’s degree in Life Sciences, Chemistry, Biology, or related field.
1–3+ years of experience in the pharmaceutical or biotech industry.
Experience working in a GMP-regulated environment.
Hands-on experience with deviation investigations and quality documentation
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