What are the responsibilities and job description for the GMP QA Specialist position at Advanced Recruiting Partners?
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 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