Executive - Production

Piramal Pharma Limited; Dhar; On-site; INR 300,000 - 600,000; Full time

Job summary

Piramal Pharma Limited is seeking an Executive - Production to oversee GCC product quality and line operations. You will allocate manpower, prevent stoppages, and participate in validation activities.

The role requires B.Pharm / M.Pharm / MSc (full time) with exposure to GMP environments, SAP data handling, and SOP training. You will drive cGMP compliance and continuous improvement on the shop floor.

Qualifications

• Bachelor or master degree in pharmacy (full-time).
• GMP/ISO and cGMP environment experience preferred.
• Knowledge of validation/qualification processes.
• Familiarity with batch changeovers and line clearance.

Responsibilities

• Maintain GCC product quality and production processes.
• Allocate manpower across workstations and manage line operations.
• Prevent machine stoppages due to manpower or breakdowns.
• Carry out validation, trials and qualifications per protocol.
• Maintain line clearances during batch/product changeover.
• Ensure c-GMP documentation and hygiene practices.
• Support calibration and maintenance of equipment.
• Enter data in SAP and generate daily reports.
• Initiate CAPA and change controls as needed.
• Train workers on SOPs and cGMP systems.

Skills

Shift supervision

GMP compliance

Quality monitoring

Documentation

CAPA deviations

Team coordination

Serialization

Education

B.Pharm / M.Pharm / MSc (full time)

Tools

SAP

Job description

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