Jithendra Bonthu

Background

About Jithendra Bonthu

I lead analytical teams working on multiple dosage forms, solve analytical lab related investigations, out of specifications data, and regularly troubleshoot GC, HPLC, ICP-MS instruments in pharmaceutical environments.> With 16+ years in pharmaceutical analytical sciences, I specialize in Quality Control, Analytical R&D, and CMC analytical regulatory compliance. I ensure all required data is available for filings, develop business by communicating with multiple clients, and suggest ways to save budget while maintaining quality.> My approach focuses on quality improvement and efficient performance by implementing 5S and lean principles. Clear communication with clients, management, and end users helps get the job done efficiently and effectively: ‍ M.S. in Chemistry ‍ Bachelor of Pharmacy ‍ Certificate in Quality Auditor Training ‍ Specialist Level Advance Course in US Regulatory Affairs-Drugs, Devices and Biologics ‍ SAS Certified Base Programmer for SAS 9 : FDA Regulations DEA Regulations cGMPs Analytical Method Development Analytical Method Validation Quality Control CMC Analytical Support : I've worked with various pharmaceutical organizations, including: Pharma Companies CDMOs CMOs CROs : Employee Recognition Awards Graduate Student Awards : Currently based in Huntington Station, NY. Open to opportunities in Long Island, NYC, New York State, New Jersey, Boston, Pennsylvania, East Coast, Midwest, Chicago, with willingness to relocate? Follow me to discuss analytical chemistry challenges, regulatory compliance strategies, or career opportunities in the pharmaceutical industry!