Mechanical Test Engineer · Virtual Incision
MSc Biomedical Engineering · University of Minnesota
I graduated with a Master's in Biomedical Engineering from the University of Minnesota–Twin Cities. With experience spanning medical device companies, pharmaceutical, and clinical data analytics, I bring a uniquely holistic perspective to healthcare innovation.
My passion lies in developing patient-centered solutions from early-stage device design to navigating complex regulatory landscapes. Beyond the lab and the code, I love traveling, getting lost in a good book and a good murder mystery!
Product Development · V&V · GD&T · SolidWorks · 3D printing · Prototyping
FDA QSR · 21 CFR 820 · EU MDR · ISO 13485 · IEC-60601 · ISO 14791
SQL · Python · PowerBI · Azure · ML · Clinical Trials · C#
cryo-EM · qRT-PCR · Flow Cytometry · Organoids · Cancer Research · Wet lab
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Virtual Incision
University of Minnesota – Twin Cities
University of Minnesota
Promed Molded Products
Shri G.S. Institute of Technology & Science
Cognizant Technology Solutions
Indian Institute of Technology
HT&IC Ltd.
Shri G.S. Institute of Technology
Shree Pacetronix Ltd.
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Virtual Incision
Virtual Incision
UMN · Masonic Cancer Center
Promed Molded Products
Cognizant · Pharmaceutical Client
Shri G.S. Institute of Technology
HT&IC Ltd.
Open to opportunities in medical device design, regulatory affairs, clinical research, and biomedical engineering.
Working in the R&D department of a surgical robotics company to test protocols, design fixtures and execute V&V activities for miniature robotic device.
Contributed to verification and validation for miniature surgical robotic subsystem to improve process validation and test methods, reducing product timeline and seamless production of the product.
Completed a rigorous two-year MSc program at one of the top biomedical engineering programs in the United States, focusing on the integration of engineering principles with life sciences to solve complex healthcare challenges.
Conducted multidisciplinary research at the intersection of computational biology and experimental science. Contributed to advancing biomedical understanding through integration of cutting-edge wet lab techniques with data-driven analysis pipelines.
Generated publishable research data and expanded the department's capabilities in multi-modal biomedical analysis across two major projects.
Worked within the QA department of a medical device manufacturer to evaluate, improve, and document manufacturing processes in alignment with FDA and international regulatory standards. Gained hands-on experience with the full quality management lifecycle.
Contributed measurable improvements to QC workflows, reducing measurement variability and strengthening the organization's regulatory compliance posture ahead of upcoming audits.
Completed a four-year honors program in Biomedical Engineering, laying the foundation for a career at the intersection of engineering, medicine, and technology. Graduated with honors recognition for academic excellence.
Supported multiple healthcare clients across clinical trial operations, data management, and regulatory compliance. Bridged technical software engineering skills with deep domain knowledge in healthcare regulations to deliver reliable, audit-ready clinical data.
Delivered clinical data solutions supporting trials across multiple therapeutic areas, achieving zero critical findings during regulatory audits for key accounts over a 2-year tenure.
Joined the Indian Institute of Technology as an R&D Intern, contributing to biomedical research initiatives within a top-tier academic environment. Gained exposure to cutting-edge scientific methodology and interdisciplinary collaborative innovation.
Worked on early-stage medical device design and development at HT&IC, contributing to the full design cycle from concept ideation through prototype validation and documentation.
Contributed to two patient-assistive device concepts, with one advancing to design freeze during the internship period.
Participated in a year-long undergraduate research project as part of the honors program, building foundational research skills while contributing to departmental investigations in biomedical device development.
Gained early industry exposure in R&D at Shree Pacetronix Ltd., a medical device company specializing in cardiac devices. Contributed to research and development activities focused on device performance and innovation.
Designed and assembled custom mechanical environmental chamber with multi-layered panels to used for testing MIRA surgical robotic system, a compact robotic platform designed for minimally invasive abdominal surgery. Work directly supports FDA 510(k) submission readiness.
Test artifacts directly contributed to design history file (DHF) documentation supporting regulatory submission milestones for the MIRA surgical platform.
Designed and assembled custom mechanical environmental chamber with multi-layered panels to used for testing MIRA surgical robotic system, a compact robotic platform designed for minimally invasive abdominal surgery. Work directly supports FDA 510(k) submission readiness.
Test artifacts directly contributed to design history file (DHF) documentation supporting regulatory submission milestones for the MIRA surgical platform.
Developed patient-derived 3D organoid models of pancreatic ductal adenocarcinoma (PDAC) to study tumor microenvironment interactions and drug response. PDAC is one of the most lethal cancers with a 5-year survival rate below 12%.
Generated a reproducible organoid biobank with matched drug response data, providing a translational platform for personalized oncology research at the Masonic Cancer Center.
Built end-to-end data engineering and visualization pipelines for a major pharmaceutical client running Phase II and Phase III oncology trials. Processed and standardized clinical data across 14 trial sites.
Pipelines processed data across 1,200+ patient records. Dashboard adopted by the clinical operations team as the primary trial monitoring interface, replacing manual Excel-based reporting.
Contributed to quality assurance protocol development for a neuromodulation catheter device used in deep brain stimulation (DBS) and spinal cord stimulation (SCS) applications. Worked within an ISO 13485-certified manufacturing environment.
Inspection protocols reduced incoming defect escape rate and were integrated into the site's quality management system for ongoing production runs.
Developed a machine learning classification pipeline to predict cardiovascular disease risk from ECG and clinical features. Undergraduate capstone research project addressing early detection of arrhythmia and coronary artery disease.
Model demonstrated potential for low-cost point-of-care screening in resource-limited settings. Work contributed to undergraduate thesis with distinction.
Contributed to the design and prototyping of a wearable biosignal monitoring device for continuous ECG, SpO₂, and skin temperature acquisition. Device targeted at remote patient monitoring and post-surgical recovery tracking.
Prototype successfully demonstrated continuous multi-parameter monitoring with <5% signal dropout over 8-hour wear sessions. Findings informed the company's next product roadmap.