Senior Imaging Software Engineer (26-394)

About the role

The Senior Imaging Software Engineer at IPG Medical Corporation is responsible for developing software solutions used in controllers and peripherals of fiber based lasers and optical amplifier products. This includes contributing to the development of complex medical instruments throughout all phases of the project, from design input to manufacturing transfer, and coordinating with overall system requirements.

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.
• Aid 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.
• Show 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.

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.
• 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.
• 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.
• 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.

Skills

• Proficiency in C++, and Python.
• Experience with Qt and/or CUDA preferred.
• Frameworks and Tools: Experience with OpenCV and at least one deep learning framework such as TensorFlow or PyTorch.

Qualifications

• Bachelor of science degree in engineering discipline, MS preferred.
• Knowledge of US and global regulatory requirements for medical devices preferred.

Pay

TBD

Schedule

TBD

Benefits

Commensurate with experience