Manager - QC

11 hours ago


Hyderabad, Telangana, India Piramal Pharma Solutions Full time ₹ 1,04,000 - ₹ 1,30,878 per year
  • Responsible to complete the work assigned and ensure the training on the activity which are assigned by supervisor/ HOD-QC prior execution.

  • Review of packing materials, raw materials, stability samples, in process and finished products data.

  • Review Qualification, Validation, Calibration data, Procedure, Audit Trail on timely manner.

  • To identify unsafe conditions/ acts inside the laboratory, report to supervisor/ HOD- QC and ensure its completeness.

  • To receive and Inward the analysis sample includes packing materials, raw

  • materials, In-process, Intermediate, API, Finished product, Stability samples and

  • make entry in to the respective AR number logs.

  • To allocate work of chemical and Instrumentation area and Ensure timely completion of work. Ensure allocated work is inline with Analyst Qualification reports.

  • Review QC Logs, Incidences, Reports and ensure document archival after released of samples.

  • Ensure Control sample inspection and Leftover sample disposal after analysis.

  • Ensure Instrument calibration and AMC done as per the schedule.

  • Prepared and Revised SOPs, Specification and Procedure in line with Regulatory requirement.

  • Conduct Training on SOPs, Trending and any other relevant procedure.

  • Prepare Stability Schedule, Stability protocol and Report, Validation/ Qualification, Trending reports.

  • Involved in Investigation and Ensure effectiveness of CAPAs.


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