"To perform In-process Quality Assurance for the process / products being manufactured in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of the products being manufactured in Main Pharma Block (Tablet/Capsule). • To give area and machine clearance i.e. checking and approval of processing areas and Equipment’s prior to start of batch processing. • To verify environmental conditions i.e. Temperature, Relative Humidity & Differential Pressure conditions are within acceptable range in all areas. • To perform and verify challenge tests at manufacturing and packing stages as per the pre-defined frequency. • To verify the status of calibration and preventive maintenance of Equipment’s used in manufacturing and packing operations. • To perform sampling of In- process and finished product as per respective MMD-I / SOP, Process validation/Hold Time/Packing Validation/Stability study as per respective protocols and to submit the samples to Quality Control for analysis.
• To notify the change control / Deviation related to shop floor activities. • To review MMD-I and release of the batches for further processing stage like Granulation, compression, coating, inspection and packing. Review and approval of Master MMD-I and BPR. • To participate in the investigation of Deviation and Market Complaint for identification of root cause and implementation of identified CAPA. • Intermediate & final Release of Finished Product in SAP. • To review & impact assessment of break down intimation slip (BDIS) and to advise precautions to be taken before, during and after attending BDIS & Closure of BDIS. • To ensure that batch must be manufactured and checked in compliance with laws in forced in that member state and in accordance with requirement of marketing authorization, registration dossier (ND). • Any other job assigned time to time by HOD."