Senior Electrical Engineer

1 month ago

Minneapolis, United States Medtronic Full time

Senior Electrical Engineer - Released Product Engineering Medtronic Neuromodulation and Pelvic Health, in Fridley, Minnesota, is currently looking for a Senior Electrical Engineer - Released Product Engineering. Bring your familiarity with low power electronics design, strong circuit analysis skills, and an understanding of test development to help us continue to engineer the extraordinary This will be a hybrid position with the expectation of being onsite at our Rice Creek, Minnesota facility three days a week. A Day in the Life As a Senior Electrical Engineer – Released Product Engineering (RPE), you will be responsible for device electrical hardware design for market released implantable neurostimulation devices and instruments. You will be involved in all aspects of patient care device electronics used as part of a system to treat neurological disorders. You will collaborate with cross-functional partners such as reliability, regulatory, operations, and sourcing colleagues to evaluate and implement design changes. Responsibilities will include but are not limited to: Circuit level design and analysis to evaluate circuit function. Identify and qualify alternate electronic components to existing design through design analysis, characterization testing and design verification.

Own product changes and change control related activities, such as conducting change impact analysis, initiating change activity (CO/CA) to update and maintain design documentation (BOM’s, Specs, drawings) etc.

Support IQ/OQ/PQ, DOE’s, SPC, Gauge R&R, Sampling methodologies, Data Analysis, Hypothesis Testing, Modeling/Predictive Analyses, Capability Studies (CpK) and Component Qualifications

Provide problem solving and troubleshooting support to manufacturing sites and key suppliers to increase yields, maintain process capability, and improve efficiency and cost.

Support cost reduction and continuous improvement projects.

Work with field returned products, conduct engineering analysis, and perform testing to determine root cause for failure.

Support Corrective & Preventive Actions (CAPA) and issue escalation including possible CAPA ownership.

Collaborate with reliability and manufacturing to determine and execute appropriate tests/assessments to evaluate supplier, process, material, design, or component changes prior to implementation.

Assist Regulatory Specialists by providing design & clinical use data and rationale to support worldwide regulatory submissions and certification renewals.

Support internal and external regulatory compliance audits.

Actively participate in new product development to RPE transfers; ensures completion of all transfer deliverables.

Interact with others on significant technical matters often requiring coordination between organizations.

Must Haves - Minimum Requirements Bachelor’s degree in a technical discipline required

Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience

Nice to Have Master’s degree in Electrical Engineering or Biomedical Engineering

Experience applying Six Sigma development methods, such as Design of Experiments (DOE), Concept Engineering (Pugh, AHP), Robust Characterization (P-Diagram), and Capability Analysis is a plus.

Strong circuit analysis and hands-on electrical testing skills experience.

Experience with complex microprocessor-based embedded systems.

Experience working with LabView.

Experience working in a regulated environment.

Experience working in a medical device work environment.

Experience using design verification and troubleshooting skills, coupled with a working knowledge of quality and statistical methods.

Experience writing engineering documents (specifications, test plans, etc).

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