Lead Embedded Systems Engineer, Medical Devices R&D

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

Job summary

Solventum, a leader in advancing healthcare technology, seeks a Principal Systems Engineer, Embedded R&D, to guide multi-disciplinary teams across mechanical, electrical, software, and quality domains in regulated product development.

You will drive system requirements, architecture, risk management, and verification strategies, coordinate with V&V, and support FDA/ISO submissions while working in a hybrid San Antonio environment.

Qualifications

• Bachelor’s degree in engineering with 7+ years in systems engineering in regulated environments.
• Alternative: HS Diploma with 11+ years in regulated systems engineering.
• 5 years in embedded electro-mechanical medical device design and testing.
• 5 years experience in GMP/UL/IEC standards for medical devices.
• 2 years System Engineering with C/C++ embedded systems, IoT, or cybersecurity risk management.

Responsibilities

• Define and manage system requirements, architecture and data flows with traceability.
• Lead design reviews, architecture decisions and verification planning.
• Support regulatory submissions (FDA/ISO) and risk management activities.
• Collaborate with V&V teams on verification strategies.

Skills

Embedded systems

Regulated design environments

System requirements & architecture

Leadership in cross-functional reviews

Education

Bachelor’s degree in engineering

High School Diploma/GED with 11+ years of experience in systems engineering in a regulated environment

Tools

C/C++ embedded systems

IoT communications

Cybersecurity risk management

Job description

Solventum, a leader in advancing healthcare technology, seeks a Principal Systems Engineer, Embedded R&D, to guide multi-disciplinary teams across mechanical, electrical, software, and quality domains in regulated product development.

You will drive system requirements, architecture, risk management, and verification strategies, coordinate with V&V, and support FDA/ISO submissions while working in a hybrid San Antonio environment.