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Staff Systems Engineer

3 months ago

Minneapolis, United States Britech Group, Inc Full time
Job DescriptionJob Description

The Staff Systems Engineer is responsible for design change analysis, analyzing system requirements, assessing design risks, testing, and making design changes for medical diagnostics instruments.

You will be a part of the Value Engineering team and report to the Senior Manager responsible for Value Engineering, Product Reliability and End-of-Life component management for legacy hardware products. If you thrive in a fast-paced and result orientated role and want to work to build a world-class design change process, project funnels and delivering high quality results - read on.

In this role, you will have the opportunity to:

  • Effectively manage project lifecycles, including analyzing requirements, developing test plans, creating project schedules, and tracking project status.

  • Ability to facilitate design reviews for hardware changes to legacy products and conduct thorough bench and system-level testing to ensure functionality.

  • Strong analytical skills, to analyze and interpret experimental data to formulate conclusions and make sound recommendations.

  • Excels at both supporting and leading cross-functional teams. And effectively collaborate with other groups to resolve issues and achieve goals.

  • Demonstrate a deep understanding of Quality, Regulatory, Manufacturing, and R&D requirements and standard methodologies. And must be able to apply this knowledge to ensure adherence to quality standards throughout the project lifecycle.

The essential requirements of the job include:

  • Bachelor’s degree in Engineering with a minimum of 9 years of experience, or master’s degree in field with a minimum of 7 years of experience, or doctoral degree in field with 4 years of experience.

  • Hands-on experience with product testing and interpreting product requirements.

  • Strong foundation in engineering principles.

  • Experience with system design and verification testing

  • Expected to travel to different Business Units to support projects in a Global Organization.

It would be a plus if you also possess previous experience in:

  • Medical regulated experience or experience in a regulated environment.

  • Experience with design change processes or new product development

  • Experience with the dFMEA process.