• Reviewed executed batch records, labels, specifications, and other production documents for commercial influenza products in compliance with FDA and international health agency requirements.• Performed disposition for incoming materials, semi-finished, and finished drug products to ensure high quality vaccines are released to market in a timely manner.• Interacted with other departments and cross functional peers to resolve batch record discrepancies and gain alignment on quality issues.• Effectively reviewed GMP documents to ensure quality attributes are met (i.e. procedures, protocols, specifications, change controls, deviations, work instructions)• Analyzed WFI testing data and environmental monitoring data to validate acceptance criteria is met.• Demonstrated strong organization skills related to priorities and workload. Solved problems both independently and within a team environment.• Assisted in training new employees and peers in both raw material and buffer release.

• Collaborated with and supported the Batch Disposition Release team assuring smooth business operations and a positive work environment. • Prepared and checked in Batch Production Records to be reviewed and archived records once released.• Organized and maintained a record filing system to reduce disorder while maximizing operational efficiency.• Manipulated systems such as SAP and GLIMS to execute reports needed for release.• Formulated and compiled data for lot release protocols.• Scanned records to submit to health authorities.