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Piramalpharma

Executive - Production

Dhar

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hirly's read of this role

Seniority
Mid level
Country
IN
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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Job Description

  • Executive - ProductionMaintenance of GCC products quality.
  • - Allocates workmen for different workstations on shift to shift basis.
  • - Ensure no stoppage of operation / machines due to non-availability of manpower and any kind of machine breakdown.
  • - Supervises the line operations and related activities and participates in Validation /Trial / qualification activities as per the protocol.
  • - Checks and cross-verify line clearance during Batch/Product changeover.
  • - Maintains c-GMP practices along with documentation in various records.
  • - To maintain good hygiene, safety practices and disciplines.
  • - Fills in-process parameters/Reconciliation in packaging documentation.
  • - Review/check BPR and other documents before submission to next stage.
  • - Involve in investigation of event/ market complaints and implementation of CAPA.
  • - Handles minor setting issues, Serialization and aggregation in machines.
  • - Monitors the speed of the machine and output according to the run time.
  • - Imparts on job/ Classroom training to the workmen/Technical staff and other employee for SOP and cGMP systems.
  • - Monitors and reports the unauthorized movement of workmen from the line.
  • - Preparation of new SOPs and updating of existing SOPs.
  • - Reports on day-to-day basis activities in SAP system (If SAP user id is available).
  • - Verifies the balances on daily and monthly basis.
  • - Maintenances and calibration of various instruments and equipment.
  • - Initiate Change controls and deviations, CAPA, Change controls in electronic system as per the need (If authorization is available).
  • - Check all the calibration tags of equipment, instruments, and fire extinguishers for their due date time to time.
  • - Knowledge and involvement in SFTI, OE & 6S Activities.
  • - Knowledge and involvement in ISO 14000 & 13485 and EHS compliance (Near Miss reporting/Learning Incident, UA & UC).
  • - Prepare and cross-verify the material return note (MRN) after the completion batch/product campaign.
  • - Prepare the line rejection note (LRN), material requisition note (MRQN) wherever required.
  • - Take-up the responsibilities of the immediate supervisor for the section in his absence

B.Pharm / M. Pharm / Msc.Full time

Original posting on Piramalpharma's site ↗

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