Description:
- Follow cGMP and GLP PRACTICES. - To ensure current positive 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 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.

📌 Assistant Manager (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka