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Associate
Posted on Aug. 27, 2025
- Ap, India
- 0 - 0 USD (yearly)
- Full Time
 
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- 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.
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