software-validation jobs in San Diego

Lead system-level validation strategy, planning, and content development for next-generation premium mobile and AI accelerator SoCs across emulation and silicon phases. Own end-to-end validation roadmaps, test coverage plans, and cross-domain content execution while partnering with architecture, design, firmware, and software teams.…See more Manage geographically distributed engineering teams, drive root-cause analysis on critical silicon and software issues, and champion AI/GenAI-driven validation methodologies. Requires 8+ years in SoC validation, strong understanding of modern SoC architectures (CPUs, memory subsystems, interconnects, power management, security), and demonstrated technical leadership.

Staff QA Engineer role at Dexcom leading quality engineering for high-volume manufacturing automation, design control, and process validation. Responsibilities include interpreting FDA 21 CFR 820 and ISO 13485 requirements, architecting validation strategies, driving design transfer for commercial deployment, leading complex investigations and CAPA initiatives, and mentoring cross-functional teams.…See more Requires deep expertise in root cause analysis, Six Sigma, process validation, statistical analysis, and data-driven decision-making across global sites.

Staff QA Engineer at Dexcom leading manufacturing quality engineering and design control for high-volume medical device automation. The role requires deep expertise in FDA 21 CFR 820 and ISO 13485 compliance, design transfer strategy, process validation, and CAPA/MRB leadership across global manufacturing sites.…See more You will mentor cross-functional teams, drive systemic quality improvements, and represent the organization during regulatory inspections, with strong emphasis on data-driven decision-making and risk-based design methodologies.

Sr Software Test Engineer I leads test projects for an automated insulin delivery system, defining schedules, developing validation test plans, and overseeing test automation frameworks and CI systems. The role requires expertise in embedded or cloud-based programming (JavaScript, C, or C#), familiarity with IEC 62304 medical device standards, and the ability to identify software architecture impacts across the platform.…See more Responsibilities include managing cross-functional test reviews, conducting software audits, assisting with failure diagnosis and replication, and preparing detailed test reports for product evaluation. The position demands 7+ years of QA/test engineering experience, with proven expertise in test automation frameworks and scripting languages.

Senior D365 F&O Developer responsible for designing, developing, and supporting Microsoft Dynamics 365 Finance & Operations enhancements and extensions, with a focus on Manufacturing and Supply Chain modules in a validated life sciences environment. The role involves leading ERP implementation initiatives, AI-driven solutions (Copilot, AI Agents), system integrations with Salesforce, Azure, warehouse management systems, and eCommerce platforms, and managing D365 biannual release upgrades including testing and deployment.…See more Requires 3+ years of D365 F&O extension development experience and 5+ years managing cloud-based D365 ERP implementations, with strong expertise in X++, data entities, OData/REST APIs, and life sciences compliance (ISO 13485).

Lead end-to-end systems engineering for tactical radio products, from requirements definition through design, integration, verification, and post-release support. Decompose system requirements into hardware, FPGA, DSP, and microprocessor subsystems; architect complex communication systems across RF, PHY, MAC, networking, and application layers.…See more Collaborate with subsystem leads, coordinate integration and validation strategies, and oversee software product validation. Provide hands-on technical support at user and developer levels, support system-level debug, and lead technical customer presentations and demonstrations.

This Staff QA Engineer role leads the design, development, validation, and deployment of Quality Assurance metric dashboards for manufacturing operations, with expertise in medical device quality management systems (QMS), regulatory compliance (FDA 21 CFR Part 11, ISO 13485), and non-conforming event management. The position coordinates site and corporate management reviews, participates in internal and external audits, and supports cross-functional teams in CAPA, risk management, and validation activities.…See more The engineer applies statistical analysis and dashboard tools (Power BI, Tableau, SQL, BigQuery) to drive quality decisions and operational excellence. Success requires direct experience with QMS, nonconforming materials, auditing, medical device regulations, and the ability to lead diverse functional groups in a fast-paced environment.