Piramal Group is a global business conglomerate with diverse interests in Pharma, Financial Services, Real Estate, and Glass Packaging. The Group has offices in over 30 countries and a global brand presence in more than 100 markets.

Led by Mr. Ajay Piramal, the Chairman, Piramal Group is a torchbearer of trusteeship and responsible business ethos. Based on the philosophy of ‘Doing Well and Doing Good’, the Group continues to create long-term value for its stakeholders and the community at large.

In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.

Position: Executive Production

Work Location:

Piramal Enterprises Limited, Plot # 67-70, Sector-II Pithampur  Dhar 454775

Job Description:

Key Roles/Responsibilities:

  • Allocation of man force for shifts at workstations.
  • Management of Manpower and Machines, Timely Maintenance, and corrective actions to ensure no disruption in work.
  • Ensures Line operations and Validation activities are in line with protocols.
  • Ensuring compliance with cGMP and Documentations of various records.
  • Fills in process parameters & manufacturing documentations.
  • Involvement in the manufacturing and documentation of Pilot batches in the existing Pilot plant in conformance with cGMP.
  • Involvement in the manufacturing and documentation of trial/pre exhibit/ exhibit /commercial batches.
  • Fills and checks BMR before submission to the superiors.
  • Handles minor parametric setting issues in various machines and products.
  • Monitors the speed of machine and output according to the run time.
  • Imparts on job/ Classroom training to the concerned workmen and supervisor for SOP and cGMP systems.
  • Imparts induction activity to all new joining.
  • Checks the compressed tablets/coated tablets/filled capsules randomly. If any discrepancy is observed, reports to superiors.
  • Monitors and reports the unauthorized movement of workmen from the line.
  • Takes up the responsibilities of the immediate supervisor for the section in his absence.
  • Verifies the balances on a daily and monthly basis.
  • Participate in machine qualification activities.
  • Checks all the calibration tags of equipment, instruments, and fire extinguisher for their due date from time to time.
  • Knowledge and involvement in SFTI & 5S Activities.
  • Knowledge and involvement in ISO 14000 & 13485.
  • Any other activity from time to time which his supervisor/company feels appropriate.
  • Checking of line clearance during the batch change over.
  • In-process testing as defined in Batch Manufacturing Record.
  • Perform a summary after completion of the sub-process like compression and coating.
  • Review quality document.

Qualification: B.Sc/B.Pharma

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