Senior Imaging Software Engineer

IPG Photonics Corp

Marlborough, MA

JOB DETAILS
SKILLS
Alliance/Partner Marketing, Budgeting, Design Verification, Economics, Employee Retention, FDA Requirements, ISO (International Organization for Standardization), Imaging Application, Intellectual Property Development, Leading Edge Technology, Manufacturing, Marketing, Medical Equipment, Medical Products, Performance Management, Peripheral Hardware, Power Amplifier, Product Costing, Product Design, Product Documentation, Product Support, Regulations, Regulatory Requirements, Requirements Management, Risk, Software Development, Software Engineering, Support Documentation, Team Player, Validation Testing
LOCATION
Marlborough, MA
POSTED
30+ days ago

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.

About the Company

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IPG Photonics Corp