What are the responsibilities and job description for the Senior Electrical Engineer position at NATUS?
Come and Join Natus Sensory, Inc.!
We are continuing to globally grow our business and are now looking to expand our team in Schaumburg, IL, USA.
Natus Sensory is a leading manufacturer of medical devices and software for a range of solutions, including eight sensory nervous systems. Our mission is to improve patient outcomes in target markets through innovative screening, diagnostic, and treatment solutions. We manufacture and distribute a range of medical device products used in the diagnosis of human disorders of sensory systems and neural pathways.
About The role
As a Senior Electrical Engineer within our R&D department, you will lead the hardware architecture and design of our global medical device portfolio. Collaborating with cross-functional teams, you will oversee hardware system architecture, embedded software/firmware development, schematic and PCB layout, design reviews, and system verification through analysis and testing. Your analytical problem-solving skills will be essential in identifying root causes, evaluating optimal solutions, and recommending comprehensive upgrades to prevent future issues. Thriving in a fast-paced environment, you will ensure projects are completed on time, meet regulatory standards, and align with our commitment to quality and innovation.
Essential Duties and Responsibilities:
· Electrical System Design and Development:
o Lead the design and development of electrical circuits, including analog and digital systems, power supplies, signal processing units, and data acquisition modules, ensuring compliance with medical device standards.
o Capture and review electrical design requirements and features, ensuring alignment with project objectives and regulatory standards.
o Create detailed schematics, select appropriate components, and oversee PCB layout using industry-standard ECAD tools.
· Prototyping and Testing:
o Develop and test prototypes to validate design concepts, identify potential issues, and ensure functionality aligns with clinical needs.
o Conduct comprehensive verification and validation testing, including risk assessments and failure mode effects analysis (FMEA), to ensure product safety and reliability.
o Ensure designs comply with Electromagnetic Compatibility (EMC) regulations by conducting necessary testing and implementing mitigation strategies.
· Regulatory Compliance and Documentation:
o Adhere to relevant regulatory standards (e.g., FDA, ISO 13485, IEC 60601-1) throughout the design and development process, including meticulous documentation and reporting.
o Review and approve technical documents related to architecture, design, and coding inspections, participating actively in cross-functional technical reviews.
· Process Improvement and Cross-Functional Collaboration:
o Suggest and implement improvements to hardware development processes, including Design for Reliability (DFR), Design for Manufacturability (DFM), and Design for Test (DFT).
o Lead the analysis of external testing results for EMC, Electrostatic Discharge (ESD), and safety testing, addressing any failures through appropriate testing or design modifications.
o Collaborate closely with cross-functional teams, including manufacturing engineers, suppliers, and production teams, to optimize designs for manufacturability and scalability.
Qualifications
· Education & Experience
o Bachelor’s or master’s degree in electrical engineering or a related field.
o Minimum of 8 years of relevant experience in hardware design and development within heavily regulated environments, preferably in the medical device industry.
· Technical Expertise
o Demonstrated leadership in driving new medical device product development projects to completion.
o Proficiency in microcontroller unit (MCU) design and board bring-up; experience with the STM32 family is a plus.
o Comprehensive knowledge of processor architecture, digital circuit design, and various communication protocols such as I2C, UART, SPI, USB, MIPI, and I2S.
o Hands-on experience in electrical safety testing and ensuring compliance with relevant standards.
o Expertise in leading hardware or firmware design through system integration, encompassing microcontrollers, analog, digital, and power design.
· Regulatory and Compliance Knowledge
o Thorough understanding of FDA Quality Systems Regulations and EU Medical Device Regulations (MDR).
o Familiarity with medical device standards and regulations, including ISO 13485 and IEC 60601.
· Other Skills
o Excellent communication skills with fluency in English, both written and verbal.
o Collaborative attitude with the ability to work effectively in a team environment.
o Strong engineering, design, and analytical skills, with a proven track record of problem-solving.
o Experience guiding medical devices from concept through commercialization, ensuring adherence to regulatory standards and successful market entry.
What we have to offer!
· The role is a hybrid position requiring 2 days of weekly physical presence in our Schaumburg Illinois office.
· Minimal travel: less than 5%
· Collaborative and international environment with different cultures.
· Compensation and Benefits: Along with a competitive salary and bonus structure, we offer a comprehensive benefit package to start on day one of employment:
o Health Benefits (Medical/Dental/Vision) visit our benefits page at: HOME | Natus Sensory
o 401k match
o 9 paid holidays including 2 “floating holidays” of your choosing,
o 4 weeks PTO
o Tuition reimbursement of up to $5,000 annually and access to our Udemy online learning platform.
o The salary range is $110,000 - $130,000 annually to start based on experience/regional cost of living and a 4% bonus.
EEO Statement
Natus Sensory is an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, veteran status, disability, sexual orientation, gender identity, or any other protected status.
Salary : $110,000 - $130,000
