

Dedicated and detail-oriented pharmaceutical professional with 3+ years of experience in production documentation and manufacturing operations. Skilled in Batch Manufacturing Record (BMR) preparation and review, Quality Management System (QMS) activities, change control, deviation handling, documentation compliance, and GMP requirements. Experienced in coordinating with cross-functional teams, including Production, Quality Assurance, and Regulatory Affairs, to ensure timely execution of manufacturing activities while maintaining the highest standards of quality and regulatory compliance. Seeking a challenging opportunity to contribute my technical expertise and commitment to operational excellence in a dynamic pharmaceutical organization.
Interpersonal Skills - Time Management, Leadership, Hardworking, Adaptability, Multi-Tasking and Attention to detail
Technical Skill- QMS (Change Control, Deviation/Investigation, BMR and supporting annexure preparation , Equipment Evaluation and Qualification, Dispensing, Packing and Manpower Handling,Training and SOP Preparation
Software - ERP,SOP Viewer, Trackwise, SAP,CipDox, Leucine , ample logic ( e-admin), Microsoft Word, Microsoft Excel, Microsoft Powerpoint, Eurotherm Reviewer Software