Senior Systems Engineer responsible for architecting, analyzing, verifying, and validating complex systems across their full lifecycle using Model-Based Systems Engineering (MBSE) methods. The role involves defining and managing system requirements, creating DoDAF architecture views using Cameo Systems Modeler/MagicDraw, performing system-level performance assessments and simulations, conducting trade studies with design-of-experiments methods, and supporting systems integration and risk management activities. The position requires 5+ years of DoD program experience with MBSE architecture modeling and requirements management, proficiency with Cameo Systems Modeler/MagicDraw, and version control tools.

Senior Software Test Engineer at Illumina responsible for designing and executing comprehensive test strategies for complex instruments in a regulated medical device environment. The role requires troubleshooting across hardware and software boundaries, working hands-on with physical laboratory instruments, and managing defects and requirements through industry-standard platforms. Candidates should have strong debugging and analytical skills, familiarity with embedded systems and communication protocols, and experience in regulated environments; AI-assisted tools and Linux command-line proficiency are valued additions.

As a Senior Software Technical Product Manager at Illumina, you will drive software design decisions for sequencing instrument platforms by translating user needs into product concepts and requirements. You'll collaborate with cross-functional teams (firmware, hardware, test) on release planning, backlog prioritization, and requirements management while creating wireframes, workflow diagrams, and formal specification documents. The role requires deep involvement in use case development, competitive analysis, risk identification (FMEA, cybersecurity), and Voice of Customer advocacy across clinical, research, and applied segments. You'll manage scope and change control for multiple concurrent instrument development efforts while ensuring compliance with medical device regulations (IEC 62304, FDA guidance) and best practices in formalized requirements engineering.