Piramal Pharma Quality Control Executive Job Opening - Apply Online
"Top Opportunity: Executive-QC Position in Medak, Telangana - Apply Now!"

Piramal Pharma Quality Control Executive Job Opening – Apply Online

Executive-QC

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 PPIC.
  • Responsible for allotting the work to the chemist within the raw material section.
  • Responsible for performing the calibrations of all instruments in the raw material section as per the schedule.
  • Responsible for maintaining all the documentation online.
  • Responsible for maintaining the minimum stock for working standards, reference standards, and impurity standards and ordering as and when required.
  • Responsible for maintaining the minimum stocks for chemicals, reagents, glass wares, and solvents required for analysis.
  • Responsible for keeping instruments neat and clean and overall housekeeping in the FP section.
  • Responsible for review of analytical data, calibration data, qualification data.
  • Responsible for keeping all instruments within the calibrated status.
  • Responsible to do the analysis, review, and release on time to support the production.
  • Responsible for reducing the lab incidences, repeat analysis, and no Data Integrity issues.
  • Responsible for real-time data monitoring.
  • Responsible for reviewing the analytical data received from external laboratory.
  • Responsible for maintaining all the calibration certificates, qualification certificates, standard weight certificates, and working/reference standard certificates.
  • Responsible for maintaining the consumption records and traceability of working/reference standards.
  • Responsible for OOS investigations, deviations, and CAPA implementations.
  • Responsible for review of SOP’s, test procedures, and specifications.
  • Responsible for providing the training on GLP/GMP to the employees working in the section.
  • Responsible for releasing the batches in a timely manner to achieve the site requirement.
  • Responsible for preparing the COA’s as per the customer requirement.
  • Responsible for approving/rejecting the batches in SAP.
  • Responsible for controlling the cost and operating within the approved budget.
  • Responsible for maintaining the instruments in working condition and reducing the breakdown time of instruments.
  • Responsible for carrying out the analytical method transfers.
  • Responsible for keeping the critical spare parts of the instruments.
  • Responsible for safe working conditions and clean environmental practices.
  • Responsible for the usage of required safety appliances in the section.
  • Responsible for SFTI.
  • Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches.
  • Responsible for training the contract persons and helpers on glassware cleaning.

Qualifications

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

APPLY ONLINE HERE

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