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Piramal Pharma | Walk-in interview for QC on 24th to 26th Dec 2020


 Job Highlights

Ensure analysis of stability samples and related documentation as per cGMP requirements

Testing and release of Raw Materials,Finished products and Packaging Materials as per cGMP requirement.

Time and Venue

24th Dec - 26th Dec, 11.00 AM - 2.00 PM

Piramal Enterprises Limited Plot # 67-70, Sector 2, District: Dhar, Pithampur, Madhya Pradesh 454 775 India 

Job Description

  • Ensure testing & release of Raw Materials, Finished products and Packaging Materials as per cGMP in time.
  • Testing and release of Raw Materials, Finished products and Packaging Materials as per cGMP requirement.
  • Ensure analysis of stability samples and related documentation as per cGMP requirement.
  • Facing Internal audits and External Audits and ensure compliance.
  • Review and approve all QC document like SOPs, STPs, GTPs etc.
  • Control of operating expenses.
  • Ensure effective implementation of systems and procedures as per GMP, GLP, ISO 9001, ISO 14001 and other regulatory requirements.
  • Carry out OOS / OOT / incident Investigation.
  • Managing of control samples.
  • To review Pharmacopeia i.e.USP, BP, IP, EP and ensure that the changes proposed are implemented and relevant PHL documents are being updated before the effective date.
  • Ensure Data entry and approval in system.
  • Set annual performance goals for Team, monitors performance and guide them to attain it.
  • On job training as necessary to develop skills and improve productivity.
  • Ensure the training to new persons as per procedure.
  • Review of laboratory data.
  • To ensure calibration & maintenance of laboratory equipment.
  • Review of work output and pending work.
  • Responsible to verify and checking of audit trail functioning of all QC instruments like HPLC, GC, UV and FTIR instrument.
  • Review and approve analytical method validation, verification and method transfer protocol, data and report.


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