Executive - Production

Piramal Pharma Ltd

India

On-site

INR 400,000 - 600,000

Full time

14 days+

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Job summary

A leading pharmaceutical company in India is looking for an Executive - Production to supervise the manufacturing of tablets and capsules. The role requires maintaining quality standards, ensuring compliance with c-GMP practices, and managing shift operations effectively. Candidates should possess a B. PHARM or B.Sc. qualification. The ideal candidate will oversee line operations, provide training to personnel, and ensure documentation is maintained accurately.

Qualifications

  • Supervises the manufacturing of quality products in compliance with c-GMP and safety standards.
  • Allocates workmen and ensures no operational stoppages due to manpower issues.
  • Maintains documentation and c-GMP practices.

Responsibilities

  • Manage shift operations and supervise quality checks.
  • Provide training to workmen on SOP and cGMP systems.
  • Monitor machine output and handle minor settings.

Education

B. PHARM / B.Sc.

Job description

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
  • 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 Qualifications
  • B. PHARM / B.Sc.Full time
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