Executive

Cadila Pharmaceuticals Limited

0 years

0 Lacs

Dholka Gujarat India

Posted:1 week ago| Platform:

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Skills Required

compliance qc stability audit lims training sequence integration data

Work Mode

On-site

Job Type

Full Time

Job Description

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.

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