Quality Assurance Specialist

We are seeking a QA Associates to support quality operations within a regulated pharmaceutical manufacturing environment. These roles are responsible for ensuring GMP compliance through batch record review, quality documentation oversight, manufacturing support, and quality systems activities.QA professionals with 3+ years GMP operations experience are encouraged apply!Location: Durham, NCPay: $30-$40/hour depending on experienceSchedule: M-F 9:00 AM-5:00 PMResponsibilitiesReview batch production records, logbooks, and inspection documentation for accuracy, completeness, and GMP compliance.Ensure documentation follows Good Documentation Practices and data integrity requirements.Support quality review and approval processes for manufacturing activities.Assist with quality investigations, deviations, CAPAs, and documentation updates as needed.Partner with manufacturing personnel to resolve documentation issues and support compliance initiatives.Maintain quality records, tracking logs, and regulatory documentation.Participate in routine manufacturing floor activities to provide QA support and oversight.QualificationsBachelor's degree in Life Sciences, Biology, Chemistry, or a related scientific discipline required.Minimum of 3 years of Quality Assurance experience in a biotechnology, biopharmaceutical, or pharmaceutical manufacturing environment.Experience supporting biologics, gene therapy, cell culture, purification, aseptic processing, or other GMP operations.Experience reviewing batch records and GMP manufacturing documentation.This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!