Associate

6 days ago

Visakhapatnam, India Pfizer Full time

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.

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