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Electrical Engineer Fellow

Job in Arden Hills, Ramsey County, Minnesota, USA
Listing for: Boston Scientific Gruppe
Full Time position
Listed on 2026-07-18
Job specializations:
  • Engineering
    Electrical Engineering, Quality Engineering
Salary/Wage Range or Industry Benchmark: 125800 - 239000 USD Yearly USD 125800.00 239000.00 YEAR
Job Description & How to Apply Below

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About the role:

The AIS Electrical Hardware R&D team is looking for an experienced Electrical Engineer Fellow with exceptional technical depth and leadership capability to provide expertise in definition, design, development and test for our active implantable medical device portfolio. As a key member of the electrical hardware design team, you will drive the creation, implementation, and continuous improvement of our electrical design of active implantable that ensure the reliability, safety, and performance of life-changing medical devices.

You will collaborate closely with process development and V&V teams to enable rapid, high-quality development and test execution of design.

Work Mode:

At Boston Scientific, we value collaboration and synergy. This role follows an onsite work model, requiring employees to be present in our Arden Hills, MN office at least four to five days per week.

Visa Sponsorship:

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Your responsibilities include:
  • Designs, develops, debugs, modifies, and tests electrical circuits and systems by using current tools, analysis techniques, and technologies.
  • Documents electrical development by writing documents, reports, memos, change requests. Methods used are determined by approved procedures and standards.
  • Establish strategies for MRI testing and evaluation of implantable devices.
  • Tracks electrical development effort by creating and maintaining records in the approved tracking management tool to include, utilizing multiple version control, defect tracking, and peer review tools including Accurev, JIRA and Windchill.
  • Solves engineering problems by analyzing the situation and recommending corrective or alternative actions.
  • Analyzes, evaluates, verifies, requirements, circuits, and systems by using engineering practices.
  • Investigates, research, selects electronic circuits, components, tools, equipment and practices.
  • Ability to perform design analysis and exploration testing.
  • Ability to work with electrical and mechanical hardware and associated tools and infrastructure.
  • Able to write final evaluation reports and work with regulatory groups to satisfy the requirements for external regulatory agencies.
  • Establishes and promotes a work environment that supports the Quality Policy and Quality System. Demonstrates a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures.
  • Solves a range of problems of varying scope and complexity, generally applying existing solutions, while exercising autonomy to propose alternatives to understanding their impact on the business or applying judgment based on experience to develop new solutions.
  • Works independently guided by company policies, guidelines and procedures, receiving guidance on complex and unprecedented problems.
  • Create schematics, layouts, BOM’s and other design outputs as needed utilizing Altium Designer.
  • Communicates clearly with cross-functional and cross-divisional stakeholders, providing concise technical updates and enabling informed decision-making.
  • Collaborate effectively with process development, quality, manufacturing, and regulatory teams to ensure comprehensive, compliant test solutions.
  • Provides technical leadership, mentoring, and direction to engineers and technicians in automation development and execution.
  • In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to all documented quality processes and procedures.
Required qualifications:
  • BS in Electrical Engineering or related field.
  • 10+ years of Electrical Engineering experience within the medical device industry or highly…
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