1) To perform online checking and review of reports of quality control department.2) To immediate reporting to QC Head for any non-conformance observed in laboratories.3) To check and verify the analytical informational in chromatographic data system before the execution of analysis.4) To monitor and record the temperature and humidity of stability room and stability incubators.5) To handle the quality management system and anticipated the investigation , review, impact assessment of change control, incident , OOS OOT and CAPA in Track wise.6) To review the instrument usage log books.7) To update the stability sample master records, registration, charging and pull out stability samples.8) To participate and provide inputs for out of specification, out of trend & lab incidents investigation conducted in QC department.9) To perform online verification of analytical activities & checking of reports.10) To review and sign off the generated electronic data in the chromatographic data systems.
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