Senior Imaging Software Engineer

IPG Photonics•Marlborough, MA

16d•Onsite

About The Position

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.

Requirements

5+ years of experience in research and development, with a focus on designing medical imaging and control systems,
Strong experience in computer vision, image processing, and image manipulation techniques
Experience with machine learning
Experience with Embedded systems and real-time systems
Proficiency in C++, and Python.
Experience with OpenCV and at least one deep learning framework such as TensorFlow or PyTorch
Ability to work independently within strict time schedules and budget boundaries, managing multiple suppliers and development partners, negotiating specifications and technical terms of the projects.
Experience preparing documentation to support rapid prototyping for pre-clinical and clinical studies.

Nice To Haves

GPU programming (CUDA/OpenCL) is preferred.
Innovative approach in development of multi-functional medical instruments including image processing / creating software documentation / writing and understanding software coding with clinical and lab experimentation.
Knowledge of Design Controls and Risk Management practices, regulations and standards, such as FDA QSR's, ISO 13485, EU MDR, ISO 14971, IEC 60601, 60825, and 62366, is preferred.
Experience with Qt and/or CUDA preferred.
Knowledge of US and global regulatory requirements for medical devices preferred.

Responsibilities

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.