eSupervisor Detail

About me

Analytical Professional with 19+ years in pharma, specializing in Method Development & Validation, Impurity Profiling, Regulatory Compliance, and QA. Experienced with HPLC, GC, FTIR, XRD & UV. Worked with Teva, Ajanta & other leading firms. Supported USFDA, WHO & TGA inspections with zero major observations. I offer students practical industry knowledge, instrument training, SOP writing, GMP compliance, and career guidance to become truly job-ready pharma professionals.

Interests: Analytical Method Development & Validation for pharmaceutical APIs and Finished Products Nitrosamine Impurity Risk Assessment and Control Strategies Elemental Impurity Profiling as per ICH Q3D Guidelines Stability Studies and Degradation Product Characterization Development of HPLC and GC methods for complex formulations Data Integrity and Quality Systems in Pharmaceutical Analysis Regulatory Compliance and ICH Guideline Implementation Green Analytical Chemistry and Sustainable Laboratory Practices