Quality Assurance Specialist (Batch Record & Disposition)

Role: QA Specialist supporting batch record and disposition activities within Regeneron's manufacturing QA team, ensuring compliance with cGMPs, SOPs, and internal standards. Responsibilities include reviewing and approving product disposition documentation, investigations, change controls, CAPAs, and controlled documents; representing QA in investigations of deviations; liaising with external partners; and supporting continuous process improvements. Requirements: B.S. in life sciences or related field; 2+ years for Associate level, 4+ years for Specialist; proven experience in GMP manufacturing QA; strong knowledge of regulatory compliance, deviations, and documentation review. Preferred: experience with raw material and laboratory investigations, mentorship skills. High-Value: biologics manufacturing, cGMP compliance, batch record review, deviation and investigation management, external partner interaction, on-site work in East Greenbush, NY, with 10% domestic travel.