Job Description Summary

Join a dynamic team working with Agile (SAFe) to develop next generation Cardiology digital applications. The Systems Engineer is responsible for leading and executing systems-level design activities for digital product development in cloud, mobile and artificial intelligence for Cardiology. This role works as a key contributor within cross functional teams to translate user needs into well defined system requirements, drive robust design execution, and support verification and validation efforts in compliance with internal processes and regulatory standards.

This role focuses on hands on technical leadership, collaboration, and disciplined application of systems engineering practices to deliver high quality, manufacturable, and serviceable products. Join this high-powered team leading advanced technology solutions at GE HealthCare!

Job Description

Roles and Responsibilities

Provide Systems Design leadership for new product development programs in Cardiology as a key contributor on a cross‑functional team.
Lead and support the engineering team in the execution of the design process, including requirements management, risk management (including FMEA), design principles including manufacturability, serviceability, reliability, testability, verification, validation, compliance with internal processes and applicable industry standards, and design transfer to production.
Participate in defining product architecture, test strategies, and design requirements, balancing performance, complexity, risk, manufacturability, serviceability, and quality.
Develop, maintain, and manage user and system requirements in alignment with product and program objectives.
Drive design evolution across multi-generation product releases with an emphasis on platforming, re-use, and reliability.
Contribute to the development and execution of verification and validation strategies for new product introduction (NPI) and changes to released products.
Support manufacturing and the installed base team through investigation and implementation of corrective and preventive actions to maintain customer satisfaction.
Develop and maintain clear requirements traceability to ensure alignment from user needs through verification and validation.
Manage requirement updates and changes throughout the product lifecycle, assessing impacts and coordinating with cross‑functional teams.
Ensure quality objectives are met and support the identification and mitigation of technical risks throughout development and post‑release.
Support regulatory and quality activities, including audits (FDA and Internal) and preparation and maintenance of Design History Files (DHFs).

Required Qualifications

Bachelor’s Degree in Computer Science or STEM-related field
Minimum of 6 years of experience in project leadership or systems engineering within a manufacturing, development, or research environment
Minimum of 3 years or experience with product development and design control processes
Demonstrated experience in product development, including requirements definition through verification and validation.
Demonstrated ability to facilitate technical trade-offs and decision making
Working knowledge of risk management methodologies, including FMEA.
Strong written and verbal communication skills.
Willingness to work a hybrid schedule with three days per week on-site at the GE HealthCare office located in Waukesha, Wisconsin
Demonstrated flexibility in approach to work hours, and willingness to partner with and accommodate global teams and schedules
Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Desired Characteristics

Master’s Degree in Computer Science or STEM-related field
7+ years of medical device or regulated product development experience.
Experience using requirements management tools to create, maintain, and trace product requirements in a collaborative development environment (e.g., DOORS, Jama, ALM).
Experience in one or more computer languages including C/C++/C#, Java, Python, or similar language
Familiarity with medical device standards such as IEC 60601‑1, ISO 14971, IEC 62304, and related regulatory and safety standards.
Organized, proactive, and results‑oriented; able to manage multiple priorities with support.
Ability to make informed technology choices when exploring technology options and analyzing the impact of technology decisions
Ability to convey technical information to cross functional program team members.
Exposure to systems engineering frameworks and methodologies, with certifications such as INCOSE ASEP, CSEP, or ESEP

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Additional Information

GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.

**Relocation Assistance Provided: **No

Job Description Summary

Roles and Responsibilities

Provide Systems Design leadership for new product development programs in Cardiology as a key contributor on a cross‑functional team.

Lead and support the engineering team in the execution of the design process, including requirements management, risk management (including FMEA), design principles including manufacturability, serviceability, reliability, testability, verification, validation, compliance with internal processes and applicable industry standards, and design transfer to production.

Participate in defining product architecture, test strategies, and design requirements, balancing performance, complexity, risk, manufacturability, serviceability, and quality.

Develop, maintain, and manage user and system requirements in alignment with product and program objectives.

Drive design evolution across multi-generation product releases with an emphasis on platforming, re-use, and reliability.

Contribute to the development and execution of verification and validation strategies for new product introduction (NPI) and changes to released products.

Support manufacturing and the installed base team through investigation and implementation of corrective and preventive actions to maintain customer satisfaction.

Develop and maintain clear requirements traceability to ensure alignment from user needs through verification and validation.

Manage requirement updates and changes throughout the product lifecycle, assessing impacts and coordinating with cross‑functional teams.

Ensure quality objectives are met and support the identification and mitigation of technical risks throughout development and post‑release.

Support regulatory and quality activities, including audits (FDA and Internal) and preparation and maintenance of Design History Files (DHFs).

Required Qualifications

Bachelor’s Degree in Computer Science or STEM-related field

Minimum of 6 years of experience in project leadership or systems engineering within a manufacturing, development, or research environment

Minimum of 3 years or experience with product development and design control processes

Demonstrated experience in product development, including requirements definition through verification and validation.

Demonstrated ability to facilitate technical trade-offs and decision making

Working knowledge of risk management methodologies, including FMEA.

Strong written and verbal communication skills.

Willingness to work a hybrid schedule with three days per week on-site at the GE HealthCare office located in Waukesha, Wisconsin

Demonstrated flexibility in approach to work hours, and willingness to partner with and accommodate global teams and schedules

Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Desired Characteristics

Master’s Degree in Computer Science or STEM-related field

7+ years of medical device or regulated product development experience.

Experience using requirements management tools to create, maintain, and trace product requirements in a collaborative development environment (e.g., DOORS, Jama, ALM).

Experience in one or more computer languages including C/C++/C#, Java, Python, or similar language

Familiarity with medical device standards such as IEC 60601‑1, ISO 14971, IEC 62304, and related regulatory and safety standards.

Organized, proactive, and results‑oriented; able to manage multiple priorities with support.

Ability to make informed technology choices when exploring technology options and analyzing the impact of technology decisions

Ability to convey technical information to cross functional program team members.

Exposure to systems engineering frameworks and methodologies, with certifications such as INCOSE ASEP, CSEP, or ESEP

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Additional Information

**Relocation Assistance Provided: **No