Executive - Production

Piramal Pharma Ltd; Dhar; On-site; INR 350,000 - 550,000; Full time

Job summary

Piramal Pharma Ltd in Dhar, Madhya Pradesh seeks a qualified supervisor to manage line operations in a GMP environment. The role involves allocating manpower, overseeing changeovers, and ensuring adherence to SOPs and cGMP practices.

You will participate in validation activities, train staff, and handle investigations and CAPA related to process deviations. Relevant pharma education is required.

Qualifications

• GMP/gxp awareness and documentation
• Batch/line changeover experience
• CAPA/Deviations handling
• 6S/OSH compliance awareness
• SAP usage for day-to-day activities

Responsibilities

• Allocate workmen for different workstations on shift to shift basis.
• Supervise line operations and participate in validation/qualification activities.
• Check line clearance during batch/product changeovers.
• Maintain c-GMP practices and records integrity.
• Train workmen and technical staff on SOPs and gC GMP systems.
• Investigate events/market complaints and implement CAPA.
• Monitor machine speed and output during runs.
• Prepare and verify MRN, LRN, MRQN as needed.

Job description

Job 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 B.Pharm / M. Pharm / Msc.Full time