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. #J-18808-Ljbffr