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.

• 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.