Senior Executive-Production

Piramal Pharma Limited; Dhar; On-site; INR 350,000 - 600,000; Full time

Job summary

Piramal Pharma Limited is seeking a Senior Executive-Production to manage line operations, allocate manpower, and ensure uninterrupted production with strict cGMP compliance.

The role involves supervision, documentation, SOP updates, CAPA handling, and training of workmen, with engagement in change controls and instrumentation calibration as required.

Qualifications

• B.Pharm or M.Pharm, full-time degree.
• Experience in pharma production operations.
• Knowledge of cGMP, SOPs and documentation.

Responsibilities

• Allocate workmen for different workstations on shift-to-shift basis.
• Supervise line operations and participate in validation, trials and qualification activities.
• Maintain c-GMP practices and documentation across records.
• Check line clearance during batch/product changeover.
• Prepare and cross-verify SOPs and update existing ones.
• Involve in investigation of events/market complaints and implement CAPA.
• Train workers and technical staff on SOPs and cGMP systems.
• Monitor machine speed and output; report deviations.
• Support calibration and maintenance of instruments and equipment.
• Initiate change controls and deviations in electronic systems as required.

Education

B.Pharm / M.Pharm

Tools

SAP

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