Performing the Audits and follow-up the compliance verification related to respective CAPA's and involved & support with Regulatory Audits to respective sites.

Key Deliverables:Responsible for the preparation of the Manufacturing BMRs & SOPs and Validation Protocols & ReportsMonitored the online Manufacturing RecordsManaged the Change control and Document control or investigationsCarried out Annual Product Quality Review (APQR)Conducted Process Validations for New Drug substances

Key Deliverables:Supervised Shift activities, Manufacturing activities, Blending process, and Multi Mill processOperated Manufacturing Equipments like Reactor, Centrifuge, Miller, Dryer and Blender.Wrote online BMRs and related Equipment usage logsEnsured and maintained the quality of manufacturing productManaged the production yieldResponsible for manpower controlHandled the activities of Finished Goods Warehouse, as and when required.TRAINING