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Teva Sr Supv Production 
India, Goa 
482928605

09.07.2025
How you’ll spend your day
  • Responsible for upkeep of Granulation area in Production.

  • Responsible for supervising the Granulation area in Production.

  • Preparation and review of SOP’s and other documentation in manufacturing areas.

  • Handling of SAP R/3 system (Manufacturing related transactions).

  • To prepare and review the investigations related to Deviations, OOS, OOT, Market complaints, Exception reports etc.

  • Signing of equipment qualification related documents as a business owner.

  • To review and ensure compliance, calibration, preventive maintenance of all machines in manufacturing areas.

  • Responsible to perform Glorya EDMS related activities.

  • Performing batch manufacturing activities as per BMR instruction.

  • Review of executed batch manufacturing records.

  • Material storage areas management.

  • Ensure Standard Operating Procedure compliance.

  • To comply with the cGMP practices.

  • Undergoing the training as per the identified training needs.

  • Training and utilization of the manpower allotted.

  • Training and development of the manpower allotted in the area to meet the business need.

  • To execute all the tasks assigned by immediate Supervisor/ HOD/ Designee.

  • Responsible for maintaining disciplined work culture in manufacturing area.

  • Management of inspection readiness Program in the Production Department.

  • Participate in the regulatory inspections and internal and external audits.

  • Identification of Shop floor related Improvement Project and implement best Practices in the Production Department.

Your experience and qualifications
  • B.Pharm / M.Pharm
  • 7-10 Years of experience