Description

• Follow cGMP and GLP PRACTICES. • To ensure current valuable 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 (India)
🏢 Cadila Pharmaceuticals
📍 India