HomeProductionSr Supervisor - VI | Manufacturing | Pfizer India | Vizag

Sr Supervisor – VI | Manufacturing | Pfizer India | Vizag


Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and the potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.

Designation: Senior Supervisor VI

Location: Vizag

Job Description:

  • Handling Visual Inspection Activities in Shifts
  • SME for Visual Inspection Equipment’s
  • Visual Inspection Process Knowledge
  • Good Communication Skills and team management skill to work with team members


  • Prepare production schedule in consultation with PPIC and functional Head.
  • Ensure Smooth operation, cleaning, and maintenance area.
  • Manage Change Parts requirements including identification of new change parts.
  • Deploy manpower optimally and conduct/ensure the on the Job training for newly joined employees.

Quality Management and Compliance

  • Implement cGMP and ensure compliance with laid down SOPs, quality system safety systems, and integrity principles at all stages of activity.
  • Participate in regulatory Audit inspections (both internal and external)
  • Support development responses to market complaints and implement corrective actions.
  • Support investigations of incidents, identify root causes, and suggest CAPA.
  • Review and approve Change controls and CAPA and finalize deviations.
  • Active participation in investigation and CAPA.


  • Review the new MMRs and Batch records
  • Prepare and review the written Procedures.
  • Batch Release closing attachments and exceptions on time.
  • Documents review and approval.

Continuous Improvement

  • Partner with the cross-functional department to identify continuous improvement initiatives (process improvement, energy efficiency, etc.)
  • Ensure the implementation of identical initiatives.

Additional Responsibilities

  • handling Internal Audit and regulatory compliance as SME.
  • Initiating Procedure and Process Simplification projects.
  • Responsible for Core Area Activities
  • Executive and Supervision of Batch Planning activities on day to day basis
  • Ensure compliance and documentation and online batch closure
  • Man Power Utilization
  • CAPA and Investigations
  • CI Loop and Tier Boards Update and Tracking Mechanism

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