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Piramalpharma

Senior Executive-Production

Dhar

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hirly's read of this role

Seniority
Senior
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

  • Senior Executive-ProductionJob Description
  • - 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 Any other activity from time to time which his supervisor/company feels appropriate.
  • Essential Qualification
  • B.Pharm / M.PharmFull time
Original posting on Piramalpharma's site ↗

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