Posted 5h ago

Senior Imaging Software Engineer

@ IPG Photonics
Marlborough, Massachusetts, United States
OnsiteFull Time
Responsibilities:developing software, ensuring compliance, documenting designs
Requirements Summary:5+ years R&D in medical imaging and control systems; expertise in computer vision, image processing, and ML; experience with embedded and real-time systems; GPU programming (CUDA/OpenCL) preferred; proficiency in C++, Python, Qt, OpenCV, TensorFlow/PyTorch; familiarity with medical device design controls.
Technical Tools Mentioned:C++, Python, Qt, CUDA, OpenCL, OpenCV, TensorFlow, PyTorch
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Job Description

IPG Medical Corporation is focused on developing next-generation medical products based on its state-of-the-art technology. Headquartered in Marlborough, MA, we aspire to work together with our employees and customers to apply light in ways that improve life.

 

Our mission is to develop innovative medical device laser solutions that make the world a better place. To accomplish this mission, we are committed to attracting and retaining the best talent and an engaged and thriving workforce that drives a sustainable future for our company and society.

 

Working at IPG Medical Group you can expect challenging projects, a motivating and friendly environment, and competitive benefits.

 

The Senior Imaging Software Engineer is responsible for working with a team of engineers to develop software solutions used in controllers and peripherals of fiber based lasers and optical amplifier products.

  • Contribute to the development of complex medical instruments through all development phases from design input through verification and validation to manufacturing transfer stages and in coordination with overall system requirements.
  • Assist in developing IP portfolio for these instruments and provide original technical solutions to improve performance, functionality, reliability, and cost requirements.
  • Develop product specifications in coordination with marketing, customers, other company departments, and contracted companies.
  • Maintain business relationships with 3rd party consultants, contractors, and suppliers. Including correspondence when the quality, timeline, or budget are at risk.
  • Sensitivity and awareness of both program budget and product costs, including clinical economics.
  • Assure products are designed to meet stringent global regulatory requirements of medical devices, such as FDA regulations, ISO 13485, CE mark for medical product and others.
  • Assist in development and maintenance of design history files and other documentation to support product regulatory approval and manufacture.