Senior Executive - Production

Piramal Pharma Ltd; India; On-site; INR 450,000 - 600,000; Full time

Job summary

A pharmaceutical company in India is seeking a Senior Executive - Production to supervise manufacturing operations, ensure compliance with c-GMP standards, and facilitate employee training. The ideal candidate holds a B. PHARM or B.Sc. and has experience in production supervision within the industry. Responsibilities include allocating work, monitoring machine operations, and maintaining documentation standards.

Qualifications

• Experience in production supervision within a pharmaceutical environment.
• Knowledge of c-GMP and documentation practices.
• Proven ability to conduct training for new employees.

Responsibilities

• Supervise quality products manufacturing in compliance with c-GMP.
• Allocate workmen for various tasks based on shift requirements.
• Monitor machine operations to ensure continuous production.
• Conduct training activities for staff to uphold SOP standards.
• Ensure all equipment is calibrated and documentation is maintained.
• 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 MRN, MRQN, LRN of Processing area.
• Review the Batch Manufacturing and other quality documents.
• To perform challenge test as per the BMR / SOP with define frequency.

Skills

c-GMP practices

Supervisory skills

Training skills

Equipment calibration

EHS knowledge

Education

B. PHARM / B.Sc.

Job description

Job Description

Senior Executive - Production

Any 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