Senior Systems Evaluation Engineer Position

4 days ago

Minneapolis, Minnesota, United States Boston Scientific Full time

Company Overview: Boston Scientific Corporation is a global leader in medical science, committed to solving the challenges that matter most. With a mission to advance science for life, we create innovative medical solutions that improve patient lives and support our employees and communities.

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Job Summary: We are seeking a highly skilled Senior Systems Evaluation Engineer to join our Cardiac Rhythm Management (CRM) Systems Engineering team in Arden Hills, MN. As a key member of our team, you will be responsible for system-level evaluation of complex implantable medical device systems, analyzing system requirements, and user needs, and performing design verification and validation activities.

Key Responsibilities:

  • Analyze system requirements, perform system interaction analysis, and coordinate system evaluation activities based on system requirements and user needs.
  • Transform requirements into test protocols and automated test scripts for end-to-end evaluation.
  • Perform design analysis and exploratory testing.
  • Work with electrical and mechanical hardware and associated tools and infrastructure.
  • Write final evaluation reports and work with regulatory group to satisfy the requirements for external regulatory agencies.
  • Develop and maintain high-quality non-medical device software tools in a regulated environment to support system design and system evaluation functions.
  • Utilize multiple version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill.
  • Apply knowledge of XML, XSD, and XSL to manage the Requirements and Test assets.
  • Track System Verification & Validation (V&V) efforts by creating and maintaining records using approved tracking management tools.
  • Conduct special studies on subjects to improve systems evaluation/engineering practices, improve system quality, subsystem partitioning, etc., by researching and identifying root cause.
  • Continuously improve System V&V processes and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow.
  • Establish and promote a work environment that supports the Quality Policy and Quality System. Demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
  • Participate in and support pre-clinical studies.

Salary Range: $120,000 - $160,000 per year

We offer a competitive salary and benefits package, as well as opportunities for career growth and professional development. Our company values diversity, equity, and inclusion and is committed to creating a workplace that is welcoming and supportive of all employees. If you are a motivated and detail-oriented individual with a passion for medical device engineering, we encourage you to apply for this exciting opportunity.

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