- 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, productive 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 Initiate change control, CAPA ,Deviation and Investigation of OOS,OOT, Incident and OOC.
- To ensure proper integration and reviewed prior to E- signature of data by reviewer • To do any other Work assign by HOD.

📌 Deputy Manager (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka