Chenna Keshava Reddy

• A result oriented pharmaceutical professional with 6+ years’ experience in industrial chemistry principles and practices across GMP, GLP and FDA regulatory environments
• Proven Track Record in Testing, Quality Control and Analytical Laboratory with strong knowledge of Laboratory Safety Standards
• Familiar with USFDA (U.S. Food and Drug Administration), WHO-cGMP (World Health Organization – Current Good Manufacturing Practices), ISO (International Organization for Standardization) and customer audits like Pfizer (US), and GSK (UK)
• Highly Experienced in Organic Chemistry, Titrations, UV-VIS Spectrophotometry, HPLC (High Performance Liquid Chromatography), and GC (Gas Chromatography)
• Proficient with software’s - LIMS, Empower – 2 & 3, EZ Chrom Elite
• Expertise in cleaning verification, cleaning validation, method development and validation