Must-HaveBachelor's Degree In Pharmaceutical or its equivalent5+ years of experiencePrior relevant experience in a regulated manufacturing operations environmentWorking knowledge of Upstream/Downstream Current Good Manufacturing Practices (cGMP) manufacturing operationsExperience on documentation and batch review process.Strong people management experienceLeadership, communication, and interpersonal skillsAbility to work in a dynamic, fast-paced and goal driven environment with strong decision making capabilityManage multiple projects and work activities (timelines, work plans, deliverables) within the team.Assist with the development of your unit from commissioning, through to start-up, validation, and {Current} Good Manufacturing Practices {part of GxP} operations.Lead System Application & Products Materials process for Shift.Perform quality check on processing activities and process confirmations of Integrated Manufacturing Excellence (IMEx) elements.Support Shift Colleagues’ Individual Development Plan.Ensure contingent staff are managed appropriately in terms of performance and training.  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Manufacturing