Biomedical Engineer Resume
Create Free Resume
Your resume is only 30 seconds away from being done.
Charles Bloomberg
PROFESSIONAL SUMMARY
Innovative Biomedical Engineer with a proven record in designing medical devices and optimizing performance through data analysis and testing. Expert in developing complex systems that enhance patient care and employing the latest technologies for the healthcare industry.
PROFESSIONAL Experience
Senior Biomedical Engineer | Company A
May 2021 — Present, Boston, USA
• Spearheaded the design and development of 3 next-generation cardio-thoracic devices that improved surgical efficiency by 30%, utilizing SolidWorks and COMSOL Multiphysics for product design and simulation.
• Led a cross-functional team in executing a project lifecycle for biomedical devices, enhancing project completion time by 20% through the implementation of Agile methodologies.
• Engineered an innovative prototype for a minimally invasive surgical instrument, reducing implementation errors by 25% via iterative testing and refinement in collaboration with surgeons.
• Achieved a 15% increase in device reliability through rigorous analysis and application of Six Sigma principles, saving the company $500K annually in manufacturer recalls.
• Managed compliance with FDA regulations and ensured that all iterations meet ISO 13485 certification, thereby securing continuous product delivery in the U.S. market.
• Led a cross-functional team in executing a project lifecycle for biomedical devices, enhancing project completion time by 20% through the implementation of Agile methodologies.
• Engineered an innovative prototype for a minimally invasive surgical instrument, reducing implementation errors by 25% via iterative testing and refinement in collaboration with surgeons.
• Achieved a 15% increase in device reliability through rigorous analysis and application of Six Sigma principles, saving the company $500K annually in manufacturer recalls.
• Managed compliance with FDA regulations and ensured that all iterations meet ISO 13485 certification, thereby securing continuous product delivery in the U.S. market.
Biomedical Engineer | Company B
June 2018 — April 2021, Seattle, USA
• Developed over 50 dynamic patient monitoring systems, integrating IoT technology to streamline data collection, which enhanced ICU efficiency by 40%.
• Collaborated with R&D teams to conduct extensive biomedical research, resulting in 3 patents for innovative healthcare devices.
• Optimized device software algorithms resulting in a 25% increase in data throughput, by programming in MATLAB and C/C++.
• Assisted in training over 200 end-users, which improved the user experience ratings by 30%, by creating detailed operational manuals and conducting live sessions.
• Collaborated with R&D teams to conduct extensive biomedical research, resulting in 3 patents for innovative healthcare devices.
• Optimized device software algorithms resulting in a 25% increase in data throughput, by programming in MATLAB and C/C++.
• Assisted in training over 200 end-users, which improved the user experience ratings by 30%, by creating detailed operational manuals and conducting live sessions.
Junior Biomedical Engineer | Company C
January 2016 — May 2018, Atlanta, USA
• Conducted comprehensive device testing for 10+ prototypes, addressing and resolving 85% of design flaws by employing Lean methodologies.
• Provided technical support for laboratory instrumentation, which led to a 15% reduction in equipment downtime.
• Collaborated with cross-discipline teams on the development of bioinformatics software, facilitating a 20% increase in data analysis accuracy.
• Provided technical support for laboratory instrumentation, which led to a 15% reduction in equipment downtime.
• Collaborated with cross-discipline teams on the development of bioinformatics software, facilitating a 20% increase in data analysis accuracy.
Biomedical Engineer Intern | Company D
June 2015 — December 2015, Orlando, USA
• Assisted in the design and testing of assistive technology devices, providing support in reducing production time by 10%.
• Developed comprehensive reports on device effectiveness, enhancing regulatory compliance submissions by 20%.
• Supported the development team in managing clinical trials data, thereby improving data integrity and analysis efficiency by 15%.
• Developed comprehensive reports on device effectiveness, enhancing regulatory compliance submissions by 20%.
• Supported the development team in managing clinical trials data, thereby improving data integrity and analysis efficiency by 15%.
Education
Bachelor of Science in Biomedical Engineering | Massachusetts Institute of Technology
May 2015
Expert-Level Skills
Biomedical Device Design, CAD Software (SolidWorks, AutoCAD), Prototyping, Biomedical Instrumentation, Data Analysis, MATLAB, C/C++, FDA Regulatory Compliance, Project Management, Problem Solving, Cross-functional Collaboration