Senior Embedded Systems Engineer, Medical Devices

Solventum; San Antonio (TX); Hybrid; USD 124,000 - 171,000; Full time

Job summary

Solventum in San Antonio, TX is seeking a Principal Systems Engineer, Embedded R&D to lead cross-functional system design for medical devices, including requirements, architecture, and verification strategies.

You will work with Mechanical, Electrical, Software, QA, and V&V teams, drive risk management, regulatory submissions, and design reviews, while ensuring traceability and compliance in a GMP/ISO environment. Hybrid work with travel and international collaboration across US/Canada.

Qualifications

• Five (5) years Demonstrated understanding and experience in design, development, and testing of embedded, electro-mechanical medical devices.
• Five (5) years experience in a regulated design environment with medical device development, FDA or ISO registered work experience.
• Five (5) years Experience in GMP certified Manufacturing Processes and UL/IEC Standards.
• Two (2) years of hands-on experience in System Engineering with products that include C or C++ embedded systems, IoT Communication, and/or Cybersecurity risk management.

Responsibilities

• Advising cross-functional teams on new product development as the technical bridge across Mechanical, Electrical, Software, Quality, and V&V teams.
• Defining and managing system requirements, architecture, interfaces, and data flows with end-to-end traceability.
• Leading system design reviews, evaluating alternatives for performance, cost, risk, and supportability.
• Reviewing technical documentation for FDA 510(k), PMA, and EU MDR submissions.

Skills

Embedded systems

C/C++

Regulated environment

V&V planning

Risk management

UI development

Wireless comms

Education

Bachelor's degree in engineering

High School Diploma/GED

Job description

Solventum in San Antonio, TX is seeking a Principal Systems Engineer, Embedded R&D to lead cross-functional system design for medical devices, including requirements, architecture, and verification strategies.

You will work with Mechanical, Electrical, Software, QA, and V&V teams, drive risk management, regulatory submissions, and design reviews, while ensuring traceability and compliance in a GMP/ISO environment. Hybrid work with travel and international collaboration across US/Canada.