Main responsibilities: * Equipment, facilities and utilities qualifications in terms of Quality (GMP, validation/verification documentation): manufacturing and packaging equipment, thermal mapping of Controlled Temperature Units (CTUs), water storage and distribution systems: PW, WFI and CS among others * Equipment and facilities periodic review evaluation * Ensure compliance with all current regulations and Pfizer Quality Standards * Participate in BOH and Corporate Internal Audits, ensuring successful with No critical findings * Meet Validation Master Plan, and production areas shut down completion on time