Perform extensive testing including black-box, white-box, security, automation, and performance testing across web, mobile, backend, and distributed systems.
Ensure tests and other tasks assigned are performed in a timely manner in compliance to Standard Operating procedures, requirements specified in our company Quality and Safety Standards, regulatory dossiers and pharmacopoeia.
Review and approve GMP documents, including SOPs, protocols, reports, and change controls, for compliance with Pfizer Global and Local Document Standards.
Analyze manufacturing and quality data to identify systemic risks, reduce recurrence of issues, improve Right First Time performance, and strengthen future manufacturing designs.