About this opportunity
ABOUT ABBOTT
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 107,000 colleagues serve people in more than 160 countries.
Staff Software Systems Engineer/ Senior Product Owner – Haifa, Israel
Leading an active lifestyle is important to the many people we serve. In Abbott’s Electrophysiology and Heart Failure division, we’re advancing the treatment of heart and vascular disease through breakthrough medical technologies in electrophysiology and heart failure, allowing people to restore their health and get on with their lives.
Position Summary:
As a Staff Software Systems Engineer and Senior Product Owner , you will provide technical leadership across software-intensive medical device systems while guiding product direction for Agile development teams. You will bridge product strategy, systems engineering, and software development to deliver innovative solutions supporting Abbott's Electrophysiology Mapping and Imaging portfolio across current and next-generation product platforms. You will be responsible for leading feature teams in the development of complex software applications that include signal processing, algorithms, and visualization in a real-time environment. You will champion cybersecurity-by-design and privacy-by-design principles throughout software development and product lifecycle activities. You will partner with Systems Engineering to translate system capabilities and architecture into software requirements, interfaces, and implementation strategies that enable scalable, maintainable, and compliant product solutions.
Primary Responsibilities:
Lead application feature definition activities working cross-functionally with Software Development, Systems Engineering, Human Factors, Clinical Engineering, and other stakeholders.
Work in an Agile environment to define product vision and priorities in alignment with organizational strategy, customer needs, clinical workflows, and technical roadmaps.
Translate product roadmap features into well-defined product requirements including features, user stories, and acceptance test criteria.
Contribute to overall project success and define necessary activities to achieve desired business results.
Identify, quantify, communicate, and proactively manage technical and integration risks that may require cross-functional collaboration to resolve complex system interactions
Lead decomposition of system requirements and architecture into software requirements, interface definitions, technical implementation strategies, traceability, and verification approaches throughout the product lifecycle.
Play a key role in the software/hardware integration. Collaborate with Systems Verification, Pre-Clinical engineering, and other stakeholders to do root cause analysis and solution generation
Review software designs to ensure alignment with system intent, software requirements, interface definitions, cybersecurity requirements, and product quality objectives.
Drive technical decision-making through requirements analysis, architecture decomposition, risk assessment, stakeholder feedback, and data-driven evaluation of software design alternatives.
Ensure that all activities conform to Quality and compliance requirements
Provide technical leadership and mentorship across multiple engineering disciplines, influencing engineering practices, technical direction, and organizational capability development.
Required Qualifications:
Bachelor’s degree in engineering (Computer, Electrical, Computer Systems, Systems, or Software), Computer Science, or related discipline
8+ years of software engineering design and development or systems engineering experience
Demonstrated expertise in C++ and object-oriented software development within complex systems.
Experience defining software-level architecture, managing technical tradeoffs, and translating system-level requirements and architecture into effective software requirements, interfaces, and software designs.
Experience serving as Product Owner or Product Manager within Agile development environments.
Experience with Agile frameworks including Scrum, SAFe, or related methodologies.
Excellent verbal and written communication skills, with ability to communicate to all levels of the organization
Preferred Qualifications:
Master’s degree in engineering (Computer, Electrical, Computer Systems, or Software), Computer Science, or related discipline
Demonstrated experience leading software development activities in compliance with IEC 62304, ISO 14971, FDA Quality System Regulations, and cybersecurity guidance for medical devices.
Medical device experience, specifically supporting cardiac mapping and/or ablation systems
Experience with medical imaging systems including echocardiography, CT, MRI, fluoroscopy, image processing, image-guided therapy, or image registration technologies.
Well versed in draft FDA Cybersecurity Guidance and GDPR
Demonstrated ability to provide technical leadership and mentorship
Experience with complex electromechanical systems including hardware, embedded firmware, disposables, and software
Job details
How this role compares
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We currently track 1231 comparable Information Technology roles across 78 biopharma companies.
Salary context
169 of 1231 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
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Seniority mix
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Therapeutic area mix
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