GMP QA Specialist

Job Summary

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.

Key Responsibilities

• 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.

Qualifications

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