Posted:6 days ago|
Platform:
Work from Office
Full Time
QA( AQA)
To review the Audit Trial Report Review of SOPs pertaining to Quality Control (Chemical & Microbiology)
Review of Stability protocols & Report
Responsible for investigation and closure of OOL, OOT & OOS.
To review the Equipment & usage log books of QC& microbiology.
To review the calibration of QC & microbiology equipments
Follow up for the closure of deviations/ change controls/CAPAs pertaining to QC area.
To log OOS, OOT and OOLs and update the relevant databases and logbooks
To Review the analytical method validation/other study Protocols, ROA and Reports
Verification of Media Fill vials.
Review of EMP, Water trends, specifications and testing
Review of STPs & GTP materials/ Product.
To prepare, review of the Quality Risk assessment documents
To prepare, review of the Annual Product Quality Review (APQR)
To review the Record of analysis pertaining to RM, PM, In process, validation samples and FP
To review the RM, PM Sampling and it approval.
only Candidates with Pharma experience/ Immediate or within 30 days joiners are requested to apply.
As per company standard
Ultra Laboratories
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