Senior Executive-Production

Piramal Pharma Ltd; Dhar; On-site; INR 600,000 - 900,000; Full time

Job summary

Piramal Pharma Ltd in Dhar (Madhya Pradesh) is seeking a Senior Executive-Production to oversee shift-based workforce allocation, line supervision, and GMP-compliant documentation. The role includes participating in validation activities, changeovers, and CAPA investigations while ensuring smooth operation and safety adherence on the shop floor.

The candidate should have B.Pharm or M.Pharm, hands-on exposure to packaging records, calibration, and SOP updates, with a proactive approach to meet

Qualifications

• Requires working knowledge of cGMP practices and good documentation habits.
• Experience in validation, qualification activities, and CAPA processes.
• Familiarity with SAP for daily reporting and batch records.

Responsibilities

• Allocates workmen for different workstations on shift to shift basis.
• Ensure no stoppage of operation / machines due to manpower shortage or breakdowns.
• Supervises line operations and participates in Validation /Trial / qualification activities as per protocol.
• Checks and cross-verify line clearance during batch/product changeover.
• Maintains c-GMP practices along with documentation in various records.
• Follows hygiene, safety practices and disciplines.
• Maintains in-process parameters and reconciliation in packaging documentation.
• Reviews BPR and other documents before submission to next stage.
• Investigates events/market complaints and implements CAPA.

Skills

cGMP

Documentation

Validation

CAPA

Troubleshooting

Training

Education

B.Pharm / M.Pharm

Tools

SAP

Job description

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