Must-Have

• Bachelor's Degree In Pharmaceutical or its equivalent
• 5+ years of experience
• Prior relevant experience in a regulated manufacturing operations environment
• Working knowledge of Upstream/Downstream Current Good Manufacturing Practices (cGMP) manufacturing operations
• Experience on documentation and batch review process.
• Strong people management experience
• Leadership, communication, and interpersonal skills
• Ability to work in a dynamic, fast-paced and goal driven environment with strong decision making capability
• Manage 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