Kunal sharma

• Monitor and verify in-process manufacturing activities to ensure compliance with GMP, SOPs, and regulatory requirements, preventing deviations and quality risks. • Conduct real-time quality oversight on sterile and non-sterile operations, ensuring documentation accuracy, batch record review, and adherence to validated processes. • Collaborate cross-functionally with Production, QA, and Validation teams to investigate deviations, implement corrective actions (CAPA), and drive continuous process improvements.

Verify prescription accuracy with the hard copy. Package or dispense appropriate compounded finished preparations, using the CIN number for confirmation. Label compounded finished preparations [Rx label, lot label and auxiliary label(s)] Run, fill and dispense utilizing an automated dispensing machine. Keep focused and on-task and operate as part of a cohesive team