Point your AI agent at freehire and let it find you a job.

Get the CLI →

Cadila Pharma

Deputy Manager

Posted Updated
Discussion
  • Follow cGMP and GLP PRACTICES.
  • To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed / implemented properly.
  • To follow safety Procedure in QC department.
  • To manage an accurate, reliable, efficient and timely review of finished products, in process/ validation, raw material, stability, GLP, Non-routine samples.
  • To ensure timely review of batch audit trail, system audit trail, message center.
  • To ensure review of Logbooks of instrument, equipment’s, columns, standards, impurities etc.
  • To review the COA of finished product in LIMS after the completion of analysis.
  • To ensure the status label updated for the instruments, equipment, glassware and workplace.
  • To conduct the training program to analyst as per the training calendar.
  • To ensure the training about the changes in standard operating procedures (SOP), if required.
  • To ensure the Sequence of HPLC/GC/IC are reviewed prior to start of the sample set.
  • To ensure methods are prepared accordingly STP/SOP.
  • To ensure proper integration and reviewed prior to E- signature of data by reviewer
  • To do any other Work assign by HOD.
Apply

See also

Management jobs by country — openings, pay and top skills →

Tailor your CV for this role?

We couldn't check your fit for this role — add a CV to your profile to see it next time.

A new version of freehire is available