Bálint Pálovics

Engineering Project Leader at MedRes - Medical Research Engineering

Bálint Pálovics is a skilled engineer with extensive experience in research and development within the medical technology sector. Currently serving as a Research and Development Engineer at MedRes since September 2022, Bálint previously worked at Novo Nordisk as a Systems Engineer and at Medtronic as a Research and Development Engineer, where significant contributions included developing prototypes and performing image post-processing for medical applications using MATLAB and Python. Educational credentials include a Master’s degree in Biomedical/Medical Engineering from DTU - Technical University of Denmark and a Bachelor’s degree in Mechanical Engineering. Bálint’s background also includes roles at Diatron Medical Instruments and MaxWell Biosystems, focusing on product development and user experience improvement.

Location

Budapest, Hungary

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MedRes - Medical Research Engineering

MedRes is a medical technology company with 20 years of experience in designing, developing, and manufacturing medical devices. We specialize in complex surgical systems, including minimally invasive handheld devices, fluid management systems, controllers and the software that controls their various functions. We offer a range of services to clients of all sizes including contract manufacturing, contract development, supply chain management, and consulting services in quality assurance, regulatory and clinical affairs. We have extensive experience in various medical specialties like gynecology, urology, cardiology, airway management, gastroenterology, and orthopedics, allowing us to handle their unique challenges and opportunities. We provide high-quality, customized manufacturing solutions for small to high volume production, from component manufacturing to the assembly of finished medical devices. Our production facility includes a Class 8 cleanroom and controlled manufacturing areas. We offer contract development services personalized for each project to guide you through all stages of medical device development. They include ideation, designing, prototyping, testing and transfer to pilot and volume manufacturing. Ensuring quality is our top priority, and our development and manufacturing processes strictly adhere to industry standards such as ISO 13485 and FDA regulations. Our QA team has deep experience in quality system development, design control processes, and regulatory requirements for market approval in the US and EU, with strong connections to clinical and academic centers. We take pride in our multiple medical devices that are currently on the market, and we are proud that many of our successful projects have been integrated into major medical device company portfolios and have gained worldwide recognition.


Employees

51-200

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