Manoj Shinde

Sr Officer @Ajanta Pharma Ltd

To perform online check & critical steps during the analysisTo review of analytical Raw data and electronic data and perform E-SIGNReview of sample set of chromatographic and spectroscopic analysisTo report any abnormalities of HOD observed during the online review To ensure the data integrity in the document generated either manually or electonicallyTo participate the review of investigation of OOS,OOT, Incident and NCR in the QC labVerification of status label on instruments/equipment in LabVerification of usage logbook for completeness and correctness To follow safty procedure in QC labEnsures the analytical data reviewed are complete,consistant and accurate through data life cycle To perform reserve sample activities I.e registration and aproval of visual inspection To ensure cGMP compliance Monitoring of documents control activities such as issuance, retrieval,storage and destruction Responsible of handle the software related to the activities mention the job role