Full-Time Contract Risk Assessment & Technical Documentation Analyst

This role addresses FDA 483 audit findings and supports specific CAPA initiatives by managing documentation development, risk modeling, and data management for high-risk manual interventions in legacy aseptic fill-finish processes. The analyst will perform RPN calculations, maintain CAPA traceability, and ensure deliverables meet year-end program goals. The position is a full-time contract through the end of the year based in Baltimore, Maryland.