Ramachandra Rao Malladhi

Supported biomanufacturing operations in cGMP environment, including upstream and downstream activities.

Executed aseptic techniques while handling materials for cleanroom production tasks.

• Assisted with batch production records (BPRs) and adhered to standard operating procedures (SOPs).
• Assisted in single-use systems and bioreactor tasks, ensuring adherence to protocols under supervision.
• Executed TFF operations for concentration and buffer exchange and supported chromatography runs on AKTA systems.
• Maintained accurate documentation to comply with good documentation practices (GDP).
• Identified deviations, reported findings, and engaged in root cause analysis discussions.
• Engaged in continuous improvement initiatives focused on enhancing safety, quality, and operational efficiency.