Innovative R&D Scientist with over 7 years of combined academic and biopharma industry experience specializing in downstream process development and purification of recombinant proteins and biosimilars. Ph.D.-qualified with extensive expertise in continuous and batch chromatography, process characterization, risk assessment, and validation in GMP-regulated environments. Proven ability to contribute to cross-functional innovation projects from early concept through technical execution and commercialization readiness. Skilled in troubleshooting complex purification challenges, optimizing processes for robustness and cost-efficiency, and ensuring regulatory compliance. Highly motivated, forward-thinking professional with a strong focus on delivering data-driven, scalable, and high-quality bioprocess solutions.
Downstream Process Development & Optimization (Affinity, IEX, MMC, HIC, SEC)
Continuous & Batch Chromatography (YMC Contichrom, BioSMB, ÄKTA Systems)
Process Characterization (DoE, JMP) & Risk Assessment
Process Verification & Validation Studies
GMP Tech Transfer & Scale-Up
Filtration Technologies (TFF, Depth, Virus Filtration)
Data Analysis & Reporting (Origin, JMP, Xpert HighScore Plus)
Scientific & Technical Writing
Cross-Functional Team Collaboration
EHS & GLP-Compliant Laboratory Practices
• 4 peer-reviewed articles in international journals (Ceramics International, Scientific Reports, Journal of Separation Science)
• Best Poster Award, ISC-2022, Hungary
• Women Leading IITM Award, 2023