Followings will be the responsibilities of the position holder: 1. Compliance of current Positive Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity compliance.
- Manufacturing and Packing process compliance in accordance with approved BMR/BPR.
- To carry out line clearance, In-process checks at the different stages of batch manufacturing and packing.
- Collection and management of control samples / stability samples / validation samples / other samples (as applicable) and maintain their record.
- Issuance of Batch records and review of executed batch documents.
- undefined 6. Issuance of controlled copies of Logbooks and formats.
- Compliance of IPQA related SOPs and records.
- Calibration of IPQA instruments and to maintain related records.
- To assist investigation activities.
- 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.