Sr. Software Systems Engineer
Medtronic2 Locations$119k – $179kPosted 7 April 2026
Job Description
We anticipate the application window for this opening will close on - 27 Apr 2026
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
Medtronic
is
seeking
a motivated and detail-oriented Sr. Software Systems Engineer to join our Affera Mapping and Ablation System team, supporting the design and development of advanced software-enabled capital systems for the cardiac electrophysiology lab.
The Sr. Software Systems Engineer will
an
integral member
in
the Affera Software Team, working on
cutting-edge
technology in the electrophysiology field. This role offers a rare chance to be at the forefront of helping develop
a groundbreaking
technology that can disrupt the industry.
The ideal candidate has strong MBSE skills and experience using
SysML
(v1/v2) to support V-model traceability from requirements through verification. They will own key features, collaborate across engineering teams, and are enthusiastic about making a meaningful difference for millions.
About the Affera Mapping and Ablation System
The Affera Mapping and Ablation System is an innovative medical technology designed to treat patients with cardiac arrhythmias. The system involves advanced mapping techniques to create detailed images of the heart's electrical activity, helping physicians
identify
abnormal areas causing arrhythmias. Once
identified , the Affera Ablation System delivers targeted energy to disrupt these abnormal signals, restoring
Primary Responsibilities
Develop and
maintain
system and software architecture models using
SysML
(v1/v2).
Apply MBSE principles to connect system intent to software services, APIs, schemas, modules, and firmware.
Define interface contracts and allocations between system functions, software, and hardware components.
Support V-model traceability across requirements, design, implementation, and verification
Author and review software system requirements with full bidirectional traceability.
Perform risk analysis activities including FMEA and interface risk identification.
Contribute to process and tooling improvements for MBSE adoption and trace automation.
Apply
the
appropriate standards , processes, procedures, and tools throughout the system development life cycle.
Required Qualifications
Bachelor's degree and
a minimum of
4
years of relevant experience
OR
Master’s
degree with
a minimum of
2
years of relevant experience
OR PhD with 0 years relevant experience
Preferred Qualifications
Knowledge of Medical Product development, IEC-62304, ISO 13485, and FDA guidance in a technical discipline, preferably software related
4 years of software verification experience
Proficient in programming languages such as Python, C/ C#
or similar languages
Experience with requirements-driven development and traceability.
Familiarity with MBSE concepts and
SysML .
Strong understanding of good documentation practices
Experience with
SysML
v2 tooling.
Experience
writing
technical reports
Experience with QT/QML
Experience with software version control systems, such as Git
Experience with Agile development
Strong work ethic and entrepreneurial drive
Ability to work effectively in a fast-paced, collaborative environment.
Strong communication
skills, both written and verbal
#LI-MDT
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii ... (truncated, view full listing at source)
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