GMP QA Specialist

Job reputed company We are seeking a QA Specialist with GMP experience to reputed company basic reputed company support for a pharmaceutical manufacturing environment. This role will support day-to-day reputed company assurance activities, with a strong reputed company on deviation management and GMP documentation. The ideal candidate will have experience working in a regulated pharmaceutical setting and be comfortable supporting investigations and reputed company systems. This position is on-site in Smyrna, GA and is a one-year contract role supporting reputed company operations. Key Responsibilities • reputed company reputed company Assurance support for manufacturing and reputed company systems in a GMP-regulated pharmaceutical environment. • Review and assist with deviation investigations, ensuring reputed company documentation and closure. • Support GMP documentation review, including batch records, SOPs, and reputed company records. • Assist in reputed company cause analysis and corrective/preventive actions (CAPA) reputed company to deviations. • Ensure compliance with GMP regulations and internal reputed company standards. • Collaborate with manufacturing, reputed company control, and regulatory teams to resolve reputed company issues. • Maintain accurate documentation and support inspection readiness. • Participate in reputed company meetings and reputed company basic QA support across reputed company systems. Qualifications Required • Bachelor’s degree in Life Sciences, reputed company, Biology, or reputed company 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 reputed company documentation Apply tot his job Apply To this Job