Followings will be the responsibilities of the position holder: 1. Compliance of current Good Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity compliance. 2. Manufacturing and Packing process compliance in accordance with approved BMR/BPR. 3. To carry out line clearance, In-process checks at the different stages of batch manufacturing and packing. 4. Collection and management of control samples / stability samples / validation samples / other samples (as applicable) and maintain their record. 5. Issuance of Batch records and review of executed batch documents. • undefined 6. Issuance of controlled copies of Logbooks and formats. 7. Compliance of IPQA related SOPs and records. 8. Calibration of IPQA instruments and to maintain related records. 9. To assist investigation activities. 10. SOP training in ISOtrain of self-train within stipulated time. • undefined 11. To follow all the practices related to safety and COBC. In absence of the position holder, designated Executive-IPQA shall be authorized designee and responsible for day to day working.