Senior Electrical Engineer at Imricor Medical Systems Inc

Burnsville, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Aug, 26

Salary

140000.0

Posted On

21 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Electrical System Architecture, Analog and Digital Circuit Design, Altium, Matlab, Octave, IEC 60601 Standards, FDA Design Controls, DFMEA, Root Cause Analysis, Verification and Validation, Good Documentation Practices, Power Distribution, Grounding and Shielding, Circuit Simulation, Board Layout, Risk Analysis

Industry

Medical Equipment Manufacturing

Description

Description Supervisor’s Title: Senior R&D Manager Exempt Status: Exempt Location: Must be able to work onsite at the Burnsville Location 5 days a week. Compensation: The expected salary/wage for this Minnesota-based position is between $100,000-140,000. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s knowledge, skills, and or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, and Retirement Benefits). Basic Function Imricor is seeking a Senior Electrical Engineer to lead the design, development, and validation of electrical systems for its MR-conditional cardiac intervention platform. The successful candidate will play a critical technical leadership role across the full product lifecycle for capital equipment and supporting subsystems - from concept and architecture through verification, validation, and deployment. This position is responsible for complying with MR safety, medical device regulations, and Imricor’s Quality Management System, and carrying out responsibilities as outlined in the environmental, health, and safety policies. Responsibilities Technical Leadership & System Design · Consults and solicits feedback from internal stakeholders to identify customer needs and translate these requirements into designs. · Leads electrical system architecture development and the design and evaluation of electrical components, enclosures, and systems to ensure availability, performance, and cost requirements are met. · Develops optimized product solutions from concept to manufacturing through risk analysis (DFMEA), prototyping, and design iterations using engineering principles, human factors/usability, and design for manufacturability practices. Verification, Validation & Testing · Defines and executes electrical verification and validation plans, including bench testing, system integration, and agency testing. Ensures electrical designs meet IEC 60601 standards and applicable FDA and CE requirements. · Leads root cause analysis and resolution of electrical issues discovered during development, verification, or clinical use. · Supports reliability testing, tolerance analyses, and design-for-manufacturability activities. Cross-Functional Collaboration & Support · Responsible for successful product launch through product development process by working cooperatively with R&D, Design Assurance, Quality, Manufacturing, Regulatory, Clinical, and Marketing. Create and execute change orders to document and implement changes. · Provides electrical engineering leadership during design reviews, risk analyses, and change control activities. · Supports manufacturing transfer, supplier technical engagement, and post-market engineering support. · Supports product life cycle by addressing supply chain and quality issues in collaboration with Operation and Quality. Documentation & Quality · Generates and maintains design documentation including input requirements, design output, risk analysis, test methods, verification and validation plans/reports, and manufacturing processes. · Contributes to design history files, risk management files, and regulatory technical documentation. · Performs other related duties and responsibilities as assigned in compliance with Imricor’s Quality Management System. Requirements Basic Qualifications · Bachelor’s degree in electrical engineering or related field (Master’s degree preferred). · 7+ years of experience in electrical engineering, with extensive experience in designing electrical systems for medical devices or capital equipment. · Strong knowledge of analog and digital circuit design, power distribution, grounding, and shielding. · Proficient computer skills including experience with schematic capture and board layout (preferably Altium), circuit simulation, and Matlab/Octave. · Working knowledge of FDA design controls and IEC 60601 standards as well as overseeing testing completed by certified test labs. · Ability to communicate concepts, ideas, and knowledge effectively and clearly to other individuals and teams. · Strong analytical and problem-solving skills. · Experience with Good Documentation Practices (GDP). Preferred Qualifications • Direct experience designing MR-conditional capital equipment. • Familiarity with MR [GS1] physics, RF systems, and electromagnetic compatibility in MR environments. • Experience supporting regulatory submissions (FDA 510k, PMA, and CE marking). • Exposure to electrophysiology, interventional cardiology, or image-guided therapy systems. Key Competencies • Strong analytical and problem-solving skills, with a proactive and inquisitive approach that drives continuous learning and improvement. • Systems-level thinking in complex, safety-critical environments. • Clear technical communication and documentation. • Ability to work effectively in cross-disciplinary, fast-paced development teams. • Commitment to patient safety, product quality, and regulatory compliance. Working Conditions · Light work, exerting up to 20 lbs. of force or less. · Requires clarity of vision at 20 inches or less (near vision) and ability to identify/distinguish colors. · Requires fingering, repetitive motion, talking, and hearing. · Requires significant viewing and working at computer a screen. · Significant work pace & pressure due to deadlines. · Requires 5% travel. The statements above reflect the principal function and most significant duties of the job as necessary for its evaluation in relation to other jobs in the organization and shall not be construed as a detailed description of all the work requirements that may be inherent in the job. Any functions that are non-Essential will be identified as such above. A request for Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. [GS1]MR physics

Responsibilities

Lead the design, development, and validation of electrical systems for an MR-conditional cardiac intervention platform. Manage the full product lifecycle from concept and architecture through verification, validation, and deployment while ensuring regulatory compliance.