Piramal Pharma Quality Control

Piramal Pharma Quality Control Executive Job Opening, Apply Online

Executive – Quality Control

Location: Medak, Telangana, India

Job Description

  • Responsible for performing the chemical and instrumentation analysis for in-process, raw materials, packing materials, intermediates, and finished products to meet the dispatch timeline as per the monthly schedule received from PPL.
  • Responsible for performing instrumentation analysis such as ICP-MS and LC-MS for in-process, raw materials, intermediates, and finished products to meet the dispatch timeline as per the monthly schedule.
  • Responsible for analytical method developments, validations, transfers, and verifications using ICP-MS and LC-MS/MS.
  • Prepare and review protocols, worksheets, and reports for method developments, validations, verifications, and transfers.
  • Allot work to chemists within the section.
  • Perform calibrations of all instruments in the section according to the schedule.
  • Maintain all documentation online.
  • Maintain minimum stock levels for working standards, reference standards, impurity standards, and order as required.
  • Maintain minimum stock levels for chemicals, reagents, glassware, and solvents needed for analysis.
  • Keep instruments clean and maintain overall housekeeping in the section.
  • Review analytical data, calibration data, and qualification data.
  • Keep all instruments within the calibrated status.
  • Perform analysis, review, and release on time to support production.
  • Reduce lab incidences, repeat analysis, and avoid data integrity issues.
  • Monitor data in real time.
  • Review analytical data received from external laboratories.
  • Maintain calibration certificates, qualification certificates, standard weight certificates, and working/reference standard certificates.
  • Maintain consumption records and traceability of working/reference standards.
  • Conduct OOS investigations, OOT, OOC, deviations investigations, and CAPA implementations.
  • Review SOPs, test procedures, and specifications.
  • Provide training on GLP/GMP to employees in the section.
  • Release batches in a timely manner to meet site requirements.
  • Prepare COAs as per customer requirements.
  • Approve/reject batches in SAP.
  • Control costs and operate within the approved budget.
  • Maintain instruments in working condition and reduce instrument breakdown time.
  • Conduct analytical method transfers.
  • Keep critical spare parts of instruments.
  • Ensure safe working conditions and clean environmental practices.
  • Use required safety appliances in the section.
  • Conduct SFTI.
  • Coordinate with QA, production, PPIC, warehouse, and TSD for smooth dispatches.
  • Train contract workers and helpers on glassware cleaning.


  • B.Sc./M.Sc., B. Pharmacy/M. Pharmacy

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