Senior Executive - Production

Piramal Pharma Ltd; India; On-site; INR 420,000 - 640,000; Full time

Job summary

Piramal Pharma Ltd. is seeking a Senior Executive - Production to oversee shift-wise manufacturing of tablets and capsules in a c-GMP compliant environment. You will allocate manpower, monitor line performance, and ensure smooth operation by preventing downtime.

The role includes training, documentation, and participation in validation and quality activities. The incumbent will supervise line staff, manage non-conformities, and support SOP development. Candidates with B.Pharm or B.Sc.

Qualifications

• B.Pharm or B.Sc. degree (full-time) is required.
• Experience in production/QA environments preferred.

Responsibilities

• Allocates workmen for different workstations on shift-to-shift basis.
• Ensures uninterrupted operation and handles machine breakdowns.
• Supervises line operations and participates in validation activities.
• Maintains c-GMP practices and documentation.
• Fills and checks BMR/BPR before submission.
• Trains workers on SOPs and c-GMP systems.
• Monitors machine speed and output.
• Takes responsibility in supervisor's absence.
• Reviews batch manufacturing records and related documents.
• Approves MRN/MRQN/LRN in processing area.
• Checks calibration tags.

Skills

c-GMP

Line supervision

Documentation

Training

Education

B.Pharm / B.Sc.

Job description

Job Description

Senior Executive - ProductionAny other activity from time to time which his supervisor/company feels appropriate. 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 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. B. PHARM / B.Sc.Full time