QA Specialist I, Drug Substance (DS)

The QA Specialist I, Drug Substance (DS) role involves performing quality assurance activities in a biopharmaceutical manufacturing environment, including observation of production processes, review of batch records, and management of deviations and investigations. The position requires ensuring compliance with cGMP and data integrity standards while supporting audits and inspections. This role also entails collaborating with cross-functional teams to resolve quality issues and maintain high manufacturing standards.