Senior Executive-Production

Piramal Pharma Ltd; Madhya Pradesh; On-site; INR 400,000 - 520,000; Full time

Job summary

Piramal Pharma Ltd in India is seeking a Senior Executive-Production to lead line supervision and ensure GMP-compliant manufacturing. The role involves managing manpower across shifts, overseeing changeovers, CAPA, and training staff on SOPs and cGMP practices.

You will also maintain documentation, participate in validation activities, and ensure calibration and maintenance of equipment while reporting in SAP where available.

Qualifications

• B.Pharm or M.Pharm degree required.
• Experience in production supervision and GMP-compliant processes.
• Familiarity with batch changeover, documentation, and CAPA processes.

Responsibilities

• Allocates workmen for line stations on shift basis.
• Prevents machine stoppages due to manpower or breakdowns.
• Supervises line operations and participates in validation activities.
• Checks line clearance during batch/product changeover.
• Maintains c-GMP practices and documentation.
• Imparts job/classroom training on SOP and cGMP.
• Prepares SOPs and updates existing ones.
• Reports activities in SAP (if user ID available).
• Initiate change controls, CAPA, deviations.
• Calibrates and maintains instruments and equipment.

Skills

cGMP

SOP

CAPA

6S

QA/QC documentation

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