•Successfully supervised day-to-day pharmaceutical production operations in full compliance with GMP, SOPs, and regulatory guidelines, ensuring zero critical audit observations.
•Achieved consistent production targets by effective manpower planning, shift management, and equipment utilization.
•Reduced batch deviations and rejections through root cause analysis and CAPA implementation, improving overall process efficiency.
•Led and trained production teams on GMP practices, safety procedures, and documentation, enhancing compliance and audit readiness.
•Ensured accurate and timely completion of batch manufacturing records (BMRs/BPRs) with minimal documentation errors.
•Coordinated with QA, QC, Engineering, and Warehouse to resolve production issues and maintain smooth workflow.
•Played a key role in successful internal, customer, and regulatory audits (USFDA/WHO-GMP/MHRA), with positive outcomes.
•Improved yield and productivity by monitoring critical process parameters and optimizing operational practices.
•Maintained strict adherence to safety and EHS norms, achieving accident-free production periods.
•Supported process validation, equipment qualification, and technology transfer activities as per regulatory requirements.