OSI Systems, Inc.
Overview
At Spacelabs Healthcare, we are committed to continuous innovation in healthcare technology to improve clinical and economic outcomes. Our scalable solutions provide critical patient data across local and remote systems, enabling better-informed decisions, increased efficiencies, and a safer environment for patients.
Why work at Spacelabs? Because lives depend on you!
Every member of our global team plays an essential role in enhancing treatment and supporting healthcare providers in delivering exceptional care. Over 60 million people benefit annually from our advancements in patient monitoring, management, care coordination, and clinical decision support.
Driven by the belief that anyone seeking care could be a member of our own family, our team is dedicated to solving major healthcare challenges, including improving patient experience, population health, reducing costs, supporting care team well-being, and advancing health equity. We pride ourselves on creating personalized services and technologies tailored to healthcare providers worldwide.
While we may not be at the patient’s bedside, their health remains in our hands.
Spacelabs Healthcare is seeking a proactive and technically skilled
Electrical Engineer III
to join our R&D team. This role is ideal for an engineer ready to take on greater ownership in designing and developing advanced medical monitoring devices. You will contribute to new product development and sustaining engineering, ensuring our solutions meet high standards of performance, safety, and regulatory compliance.
This is a hybrid position requiring employees to work 3 days/week at our headquarters in Snoqualmie, WA.
Responsibilities
Design, develop, and test analog and digital circuits for medical devices
Own key subsystems or modules in product development, from concept to production
Perform schematic capture, guide PCB layout, select components, and conduct simulations
Troubleshoot and resolve electrical issues in new and existing designs
Collaborate with firmware, mechanical, software, and manufacturing teams
Support regulatory compliance efforts including IEC 60601, ISO 13485, and FDA requirements
Develop and execute test plans, validation protocols, and documentation
Mentor junior engineers and contribute to design reviews and technical discussions
Participate in sustaining engineering and continuous improvement initiatives
Ensure adherence to quality management systems and documentation standards
Uphold company values of Integrity, Innovation, Accountability, and Teamwork
Report quality problems or defects for corrective actions
Duties may be modified or assigned as needed
Qualifications
Bachelor’s degree in Electrical or Biomedical Engineering or related field
5+ years of engineering experience, preferably in medical devices or regulated industries
Proficiency in analog and digital circuit design, low-noise and low-power systems
Experience with PCB design tools (e.g., Altium, OrCAD) and SPICE simulation software
Experience with multi-layer PCB layout, grounding, EMI/EMC practices
Experience with embedded systems, sensors, microcontrollers, and signal processing
Ability to review or develop embedded C/C++ firmware
Design of power supplies, battery management, and isolation techniques preferred
Ability to generate design history files, technical files, and risk assessments
Experience working under a QMS and developing verification and validation protocols
Understanding of IEC 60601, ISO 13485, FDA QSR standards; lab equipment experience preferred
Strong documentation, communication, and collaboration skills
Experience with embedded systems development and verification preferred
Knowledge of DFM and design transfer to manufacturing
Familiarity with Agile methodologies and project management tools
Ability to work effectively in cross-functional teams
Track record of taking designs from concept to production in regulated environments preferred
Experience with FDA or EU MDR design control processes preferred
#LI-Hybrid #LI-TC1
Benefits :
Life at OSI
Benefits vary based on location and hire date. Salary is a general guideline, influenced by experience, qualifications, and market conditions.
Notice to Third Party Agencies OSI Systems does not accept unsolicited resumes. Resumes submitted without an agreement are property of OSI and may be used without obligation.
Equal Opportunity Employer Disability and Veteran status are considered in employment decisions.
Know Your Rights
#J-18808-Ljbffr
At Spacelabs Healthcare, we are committed to continuous innovation in healthcare technology to improve clinical and economic outcomes. Our scalable solutions provide critical patient data across local and remote systems, enabling better-informed decisions, increased efficiencies, and a safer environment for patients.
Why work at Spacelabs? Because lives depend on you!
Every member of our global team plays an essential role in enhancing treatment and supporting healthcare providers in delivering exceptional care. Over 60 million people benefit annually from our advancements in patient monitoring, management, care coordination, and clinical decision support.
Driven by the belief that anyone seeking care could be a member of our own family, our team is dedicated to solving major healthcare challenges, including improving patient experience, population health, reducing costs, supporting care team well-being, and advancing health equity. We pride ourselves on creating personalized services and technologies tailored to healthcare providers worldwide.
While we may not be at the patient’s bedside, their health remains in our hands.
Spacelabs Healthcare is seeking a proactive and technically skilled
Electrical Engineer III
to join our R&D team. This role is ideal for an engineer ready to take on greater ownership in designing and developing advanced medical monitoring devices. You will contribute to new product development and sustaining engineering, ensuring our solutions meet high standards of performance, safety, and regulatory compliance.
This is a hybrid position requiring employees to work 3 days/week at our headquarters in Snoqualmie, WA.
Responsibilities
Design, develop, and test analog and digital circuits for medical devices
Own key subsystems or modules in product development, from concept to production
Perform schematic capture, guide PCB layout, select components, and conduct simulations
Troubleshoot and resolve electrical issues in new and existing designs
Collaborate with firmware, mechanical, software, and manufacturing teams
Support regulatory compliance efforts including IEC 60601, ISO 13485, and FDA requirements
Develop and execute test plans, validation protocols, and documentation
Mentor junior engineers and contribute to design reviews and technical discussions
Participate in sustaining engineering and continuous improvement initiatives
Ensure adherence to quality management systems and documentation standards
Uphold company values of Integrity, Innovation, Accountability, and Teamwork
Report quality problems or defects for corrective actions
Duties may be modified or assigned as needed
Qualifications
Bachelor’s degree in Electrical or Biomedical Engineering or related field
5+ years of engineering experience, preferably in medical devices or regulated industries
Proficiency in analog and digital circuit design, low-noise and low-power systems
Experience with PCB design tools (e.g., Altium, OrCAD) and SPICE simulation software
Experience with multi-layer PCB layout, grounding, EMI/EMC practices
Experience with embedded systems, sensors, microcontrollers, and signal processing
Ability to review or develop embedded C/C++ firmware
Design of power supplies, battery management, and isolation techniques preferred
Ability to generate design history files, technical files, and risk assessments
Experience working under a QMS and developing verification and validation protocols
Understanding of IEC 60601, ISO 13485, FDA QSR standards; lab equipment experience preferred
Strong documentation, communication, and collaboration skills
Experience with embedded systems development and verification preferred
Knowledge of DFM and design transfer to manufacturing
Familiarity with Agile methodologies and project management tools
Ability to work effectively in cross-functional teams
Track record of taking designs from concept to production in regulated environments preferred
Experience with FDA or EU MDR design control processes preferred
#LI-Hybrid #LI-TC1
Benefits :
Life at OSI
Benefits vary based on location and hire date. Salary is a general guideline, influenced by experience, qualifications, and market conditions.
Notice to Third Party Agencies OSI Systems does not accept unsolicited resumes. Resumes submitted without an agreement are property of OSI and may be used without obligation.
Equal Opportunity Employer Disability and Veteran status are considered in employment decisions.
Know Your Rights
#J-18808-Ljbffr