1. To perform audits in production department as per IPQA protocol. 2. Sampling and verification of RM/PM. 3. To supervise BMR, BPR, COA, RM COA at company site as per respective product. 4. Executing customs Bevac and product dispatch at factory. 5. Troubleshooting of deviations occur on site. 6. Performing godown visit for product checking/ assisting in product checking during outside Lab inspection. 7. Performing Factory visit on receipt of any complaint from QA(H.O)/CUSTOMER, carrying out corrective action at site as per decision of manager/seniors. 8. Miscellaneous tasks as assigned by the reporting officer and/or the management (As & when required)
1. Approval of IPQA activities for tablet, liquid & ointment manufacturing along with necessary documentation to name a few. 2. Documents archival and retrieval (Log book, BMR, BPR). 3. Monitor production process for quality and productivity and maintain the quality and productivity. 4. Sampling of process validation samples as per approved validation protocol.
1. IPQA, verification & monitor product line setting and troubleshooting. 2. To conduct routine and spot inspection. 3. Preparing and verification BMR, BPR, MFR, SOP etc. 4. Maintain control sample record. 5. Maintain artwork record & verification.