

Accomplished biotechnology scientist with 10+ years of cross-disciplinary expertise spanning bioprocess development, analytical method validation, regulatory compliance, and biologics innovation. PhD candidate in Biotechnology (submission Oct 2026) integrating computational biology, multi-omics analysis, and machine learning with deep wet-laboratory expertise. Proven record of scaling complex biologics processes including lentiviral vectors (LVV) and adeno-associated virus (AAV) platforms for Cell & Gene Therapy (CAR-T), alongside large-scale vaccine development (COVID-19, PCV, MCV, Hepatitis-B, HIB, DPT, Pentavalent). Seasoned regulatory scientist with successful audit engagements across WHO, US-FDA, EU-GMP, TGA, ANVISA, CDSCO, and S-FDA frameworks. Executed international technology transfer across 8 countries (Germany, Russia, Egypt, Malaysia, Saudi Arabia, Iran, Cuba, China). BIRAC E-YUVA invited speaker and BioNEST bioprocessing trainer, uniquely positioned to translate deep scientific research into commercially viable, patent-grade innovations.
Integral University, Lucknow | Jul 2023 - Oct 2026
Research focus: Identification of small molecule potential inhibitor against oncogenic Protein. Multi-omics data integration, cancer genomics, and ML-driven biomarker discovery.
Institute of Engineering and Technology (AKTU, Lucknow) | Jul 2017 - Oct 2019
Thesis: Purification and characterization of anti-tubercular compounds from Coriandrum-Sativum and its mode of action.
Integral University, Lucknow, Uttar Pradesh | 2011 - 2015
Dissertation: Antibiotic Assay Validation (Bleomycin for Injection)
Co-Founder & CTO | In Progress
Developing Hygro-Responsive Plant Extracellular Vesicles (HR-PEV) — a climate-adaptive, plant-derived nanocarrier platform for cosmetic actives. Patent-first model targeting BIRAC BIG grant and BioNEST incubation.
Manager, Process Development (R&D) | Feb 2023 - May 2026
Cell & Gene Therapy scale-up (LVV production to 2-cell stack, 10⁹-10¹⁰ TU/ml), PEI transfection reagent formulation, AAV/LVV platform leadership for CAR-T therapy.
Senior Executive, Quality Control (R&D) | Jul 2021 - Feb 2023
Vaccine analytical development (SARS-CoV-2 S1 and N proteins, Bivalent COVID-19). Multi-vaccine platform R&D (Hepatitis-B, PCV, MCV, Meningococcal, DPT/Pentavalent). International technology transfer to Russia, Iran, Turkey, Egypt.
Technical Officer - Biotechnology | Jul 2019 - Jul 2021
Cell biology platforms (tissue culture, primary human cells, iPSC culturing and transfection). Assay development (ELISA, Flow Cytometry, SDS-PAGE, Western Blot, advanced imaging).
Asst. Manager / Executive Microbiologist / Management Trainee (QC) | May 2015 - Apr 2017
Regulatory audit success (EU-GMP, GLP, S-FDA, TGA, WHO). Microbiology & compliance (sterility analysis, bacterial endotoxin testing). Analytical QC (antibiotic and chromogenic assays, trend analysis).
Expert in LVV/AAV process development for Cell & Gene Therapy (CAR-T), vaccine manufacturing (upstream & downstream), PEI transfection reagent formulation, and GMP-grade biologics manufacturing including vaccines, polysaccharides, and conjugates.
Specialized in ELISA, SDS-PAGE, Western Blot, Sec-HPLC, Flow Cytometry, Bacterial Endotoxin Testing, Sterility Analysis, Antibiotic & chromogenic assays, and protein/sugar content estimation for vaccines and biologics.
Successfully executed end-to-end technology transfer of vaccines and analytical platforms to 8 countries: Germany, Russia, Egypt, Malaysia, Saudi Arabia, Iran, Cuba, and China, with comprehensive GMP & QMS training delivery.
Clean audit track record across WHO, US-FDA, EU-GMP, TGA, ANVISA, CDSCO, S-FDA, and GLP frameworks. IQ/OQ/PQ equipment qualification, SOP/STP validation, Quality Management Systems design, EUA, GRPs, and Pharmacovigilance expertise.
Multi-omics data integration (genomics, transcriptomics, proteomics), cancer biomarker discovery using machine learning, bioinformatics pipeline development, in-silico assay design, and infectious disease modeling.
Mammalian cell culture, iPSC culturing & transfection, primary human cell work, tissue culture, FACS, and cellular/biochemical assay development for research and therapeutic applications.






Select Sector
Leverage 10+ years of cross-disciplinary expertise in bioprocess development, regulatory compliance, and technical implementation across Cell & Gene Therapy, Vaccines, Pharmaceuticals, and Cosmeceuticals.
Practical insights into scaling LVV production to clinical-grade specifications (10⁹-10¹⁰ TU/ml) for CAR-T immunotherapy.
Developing novel, cost-effective PEI-based transfection reagents while maintaining batch-to-batch consistency.
Leveraging genomics, transcriptomics, and proteomics with machine learning for oncology applications.
Lessons learned from executing successful technology transfer across Germany, Russia, Egypt, Malaysia, Saudi Arabia, Iran, Cuba, and China.
From Bivalent COVID-19 to PCV, MCV, Hepatitis-B, and Pentavalent vaccines: strategies for process development and GMP compliance.
Comprehensive audit preparation strategies with clean track record across multiple regulatory frameworks.
Advanced techniques for induced pluripotent stem cell culturing and high-efficiency transfection workflows.
Process development and analytical method validation for adeno-associated virus platforms used in gene therapy.