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Piramal pharma solutions

Executive - Production

13 May 2026

Full-Time Tamil Nadu

Department

Health & Biotech

Job Category

Health & Biotech

Description

  • Operating all process equipments Viz. Hydrogenator, Reactor, centrifuge, Tray drier, Vacuum Tray drier / Roto cone vacuum drier / Agitated nutsche filter cum drier / Multi mill / Sifter / Distillation column etc., utility equipments viz. vacuum pump, Ejectors, scrubbers etc. in shifts.
  • Safe handling of hazardous chemicals, solvents, catalyst
  • Knowledge on static electricity and its controls
  • Monitoring & controlling the process parameters as per BMR
  • Execution of production batches and meeting the production targets
  • Effective utilization of men, utility, equipment, raw materials and power
  • Maintaining Good Housekeeping in work place all the time and maintaining the assets in good condition.
  • Online Documentation viz. batch manufacturing record, equipment cleaning record etc.
  • Identifying and reporting of abnormalities
  • Reporting of near miss, unsafe condition, unsafe act
  • Packing of Solid / liquid products as per requirement
  • Maintaining the inventories of raw material, packing material, solvents, intermediates, finished goods
  • Trouble shooting of process equipments, utility systems and process
  • Initiating work order and safety permits
  • Adherence to CGMP and safety norms
  • Knowledge in ISO 9001, ISO 14001, ISO 45001
  • Generating new ideas and initiatives
  • Involving Yield improvement, time cycle reduction, capacity enhancement initiatives
  • Making the plant for the audit readiness
  • Carrying out the activities in line with patient centric approach
  • Ensuring the safety of self, operating personnel and workmen associated
  • Co ordination with the supporting departments viz Engineering, QC, R&D for smooth running of production.
  • Participation in training programme and effective communication process

Qualifications

  • Qualification: DCT / B.Sc. in Chemistry / M.Sc. in chemistry
  • Work Experience: 4–6 years experience in Bulk Drugs Industry and exposure to GMP
  • Special Requirements: Exposure to FDA guidelines

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