Executive - Production

Piramal Pharma Ltd; India; On-site; INR 500,000 - 800,000; Full time

Job summary

Piramal Pharma Ltd. is seeking an Executive - Production to supervise quality tablet and capsule manufacturing on a shift basis. The role emphasizes adherence to c-GMP, safety, and hygiene, with responsibilities spanning manpower allocation, line supervision, and document control.

You will participate in validation activities, maintain production records, train staff, and ensure smooth line clearance during batch changes, while monitoring equipment and process performance.

Qualifications

• Experience in supervising production lines in a pharmaceutical setting.
• Familiarity with Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
• Knowledge of EHS, 6S and ISO 14000 & 13485 standards.

Responsibilities

• Allocates workmen for different workstations on a shift basis.
• Ensures no stoppage due to manpower or machine breakdown.
• Supervises line operations and participates in validation activities.
• Maintains c-GMP practices and documentation across records.
• Fills and checks BMR/BPR before submission to seniors.
• Handles minor parametric setting issues on machines and products.
• Monitors machine speed and output during run time.
• Provides on-the-job and classroom training on SOPs and cGMP.
• Inducts new joiners and monitors line movements.
• Assists supervisor in absence and helps prepare SOPs.
• Verifies daily and monthly balances and calibration tags.

Skills

Supervisory

Quality awareness

c-GMP familiarity

Safety and hygiene

Education

B.Pharm / B.Sc. (Full time)

Job description

Executive - ProductionJob Description

Supervises quality products are being manufactured (Tablets and Capsules Inspection) in conformance with c-GMP / Safety and hygiene requirements on shift-to-shift basis. Maintains overall disciplines and productivity. Key Responsibilities Key Roles/Responsibilities:

• 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 participate in Validation activities as per the protocol.
• Maintains c-GMP practices along with documentations in various records.
• Fills and checks BMR / BPR before submission to the superiors.
• Handles minor parametric setting issues in various machines and products.
• Monitors speed of machine and output according to the run time.
• Imparts on job / Classroom training to the concern workmen and supervisor for SOP and cGMP systems.
• Imparts induction activity to all new joining.
• Monitors and reports the unauthorized movement of workmen from line.
• Takes up the responsibilities of the immediate supervisor for the section in his absence.
• Helps section in charge in preparation of SOP.
• Verifies the balances on daily and monthly basis.
• Checks all the calibration tags of equipment, instruments, or fire extinguisher for their due date time to time.
• Knowledge and involvement in EHS, SFTI & 6S Activities.
• Knowledge and involvement in ISO 14000 & 13485.
• Any other activity from time to time which his supervisor / company feels appropriate.
• Checking of line clearance during batch change over.
• In process testing as defined in Batch Manufacturing Record.
• Approval of Material Return Note (MRN), Material Requisition Note (MRQN), Line rejection Note (LRN) of Processing area.
• Review the Batch Manufacturing and other quality documents.
• To perform challenge test as per the BMR / SOP with define frequency. Essential Qualification B. PHARM / B.Sc.Full time