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Cadila Pharma

Manager

Posted Updated
Discussion
  • Responsible for review the Stability Section Reports
  • To ensure the compliance of GLP in Quality Control Lab.
  • To plan the analysis and trouble shooting in absence of supervisor.
  • Responsible for review of stability protocol and Stability data as per requirement.
  • Responsible for timely review the data of stability sample and as per monthly calendar.
  • Responsible for timely complete the analysis as per Stability management SOP.
  • Responsible for handling and investigation of OOS, OOT and Incidence.
  • To review the instruments log books related to Stability document if required.
  • Responsible for monitoring daily routine activity & follow good documentation practices.
  • To ensure the column usage and record’s of impurities and working standard/ reference standard during stability samples analysis.
  • To review the COA, STP, SOPs and other master documents. (as per requirement)
  • To provide all the necessary data to production, regulatory and QA.
  • To ensure that the stability section i.e. sample room and stability chamber always kept clean and presentable at all time.
  • To do all the activities as per the instructions of immediate senior as well as management.
  • Responsible for review the Stability Section Reports
  • To ensure the compliance of GLP in Quality Control Lab.
  • To plan the analysis and trouble shooting in absence of supervisor.
  • Responsible for review of stability protocol and Stability data as per requirement.
  • Responsible for timely review the data of stability sample and as per monthly calendar.
  • Responsible for timely complete the analysis as per Stability management SOP.
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