1 Responsible for the Handling of market complaint at site 2 Responsible for the Handling of Deviation management at site 3 Responsible for the Handling of CAPA and Global CAPA management and effectiveness checking at site 4 Responsible to co-ordinate the execution of mock recall and market recall 5 Responsible to review and tracking of Audit Responses 6 Responsible to raise review and tracking of Quality Alert 7 Responsible to ensure timely closure of QMS documents 8 To perform activity as per authorization in EDMS LMS and TRACKWISE software 9 Responsible for performing IPQA activities 10 To perform process validation and cleaning validation sampling activity in shop floor 11 To review recent exhibit transfer and executed master BMR s and BPR s 12 To review batch records and associate annexures checklists etc 13 To perform Product Recipe approval SFG FG release sampling sample posting etc in SAP HANA systems 14 To prepare and execute hold time study protocol and perform sampling activity 15 To prepare and review process validation protocol and report 16 Preparation and Review of Annual product quality review

📌 Senior Officer (Guwahati)
🏢 Sun Pharmaceutical Industries
📍 Guwahati