risk-analysis jobs in San Diego

Senior Systems Engineer responsible for defining and maintaining system-level architectures for complex medical devices, including interface control documentation across fluidic, mechanical, electronics, software, and human factors subsystems. The role involves modeling system behavior using functional modeling techniques (SysML, functional block diagrams, state machines), conducting trade studies, and validating architectural assumptions through testing and characterization.…See more Requires partnering with cross-functional engineering teams to ensure subsystem alignment, supporting design controls per 21 CFR 820.30 and ISO 13485, and mentoring engineers on systems thinking and interface definition. This is a hands-on role grounded in bench-top testing, data analysis, and evidence-based architectural decisions rather than paper-only work.

Principal Technical Program Manager at Intuit responsible for transforming program management through AI-driven predictive insights, continuous visibility, and proactive risk identification. The role requires leading complex, large-scale technical programs across matrixed organizations, translating business and technology strategy into executable plans, and establishing repeatable frameworks that scale impact across the organization.…See more You will leverage AI tools as strategic thought partners to accelerate decision-making, surface emerging risks, and enhance execution while maintaining accountability through sound judgment and stakeholder context. Success demands systems-thinking, the ability to influence at all levels, and demonstrated expertise in building scalable operating mechanisms that improve organizational effectiveness.

The Sr. Beacon Application Analyst designs, builds, tests, and implements Epic's Beacon oncology/infusion module and related clinical systems at UC San Diego Health.…See more The role requires expert knowledge of Epic Beacon and infusion workflows, with responsibility for adapting software to meet clinical needs, creating protocols, writing detailed specifications, and providing technical leadership on medium-to-large projects. This is a hybrid position requiring 9 years of related experience or a Bachelor's degree plus 5 years of experience, with advanced skills in problem-solving, clinical process knowledge, project management, and cross-functional collaboration.

Systems Engineer responsible for translating market and user needs into clear requirements across biology, hardware, and software subsystems at an early-stage cell-therapy manufacturing startup. Owns requirements management, interface control documentation, and system block diagrams to keep multiple engineering teams aligned during prototype development.…See more Leads verification, validation, and risk analysis planning; supports design reviews and regulatory compliance through design history file maintenance. Expects hands-on involvement in prototype assembly, testing, and cross-disciplinary problem-solving in a research-to-product transition environment.

This Systems Engineer role owns the requirements, interfaces, and risk management for an early-stage cell-therapy manufacturing platform spanning hardware, software, and biology. You will maintain requirements in dedicated tools, define and document interfaces between mechanical, electrical, fluidic, software, and cell-biology subsystems, support verification and validation planning, and coordinate across multiple engineering teams.…See more The role requires 5+ years at the intersection of biology, chemistry, and instrumentation, with hands-on lab experience and proven ability to run design reviews and resolve cross-team conflicts.

The Systems Engineer applies systems engineering discipline to define, develop, integrate, and test complex in vitro diagnostic medical devices. Responsibilities include capturing user requirements, authoring system and subsystem requirements documentation, conducting hazard and risk analysis, managing configuration and change control, driving system integration and root-cause analysis, and coordinating with development, testing, clinical, and cross-functional teams.…See more The role requires a BS in engineering, 10+ years of industry experience, proven medical device development background, and proficiency in systems engineering methodologies including requirements decomposition, architecture, design reviews, and risk management.

Lead the full system development lifecycle for government programs, from requirements analysis and design through verification, validation, and sustainment. Manage requirements decomposition, allocation, and traceability; define system architecture and CONOPS using Model Based Systems Engineering (MBSE) methodologies; identify and mitigate technical risks associated with secure hardware; and produce comprehensive technical documentation.…See more Participate in customer meetings and technical interchanges; requires 12+ years of systems engineering experience, a Bachelor's degree in Systems Engineering or related field, and demonstrated expertise in requirements management, MBSE, the V-model, and Risk Management Framework (RMF) on medium-to-large DoD programs.

Sr. Systems Engineer at Globus Medical responsible for complex medical device system development, leading cross-functional coordination across software, hardware, clinical, regulatory, and manufacturing teams.…See more The role requires decomposing intricate systems, troubleshooting subsystem interactions, conducting risk analysis per ISO 14971, and driving continuous improvement through design of experiments and root cause analysis. Requires 5+ years in complex system development (medical devices, robotics, or similar) with strong systems engineering principles, FDA-regulated product development experience, and ability to translate technical concepts across multidisciplinary disciplines.

Senior Manager leading systems engineering for complex Point-of-Care diagnostic instruments, overseeing hardware, software, consumable, and assay integration. Responsible for system architecture, cross-functional integration with external partners, regulatory compliance (ISO 13485, IEC 62366, IEC 60601, ISO 14971), and risk analysis.…See more Will mentor junior engineers, drive technical decision-making across R&D, Quality, Manufacturing, and Regulatory teams, and manage the full product lifecycle from concept through commercial launch in a regulated environment.

The Systems Engineer applies interdisciplinary expertise to define, develop, integrate, and test complex In Vitro Diagnostic systems for medical device applications. Responsibilities include documenting user and system requirements, decomposing system architecture into subsystems with defined interfaces, conducting hazard and risk analysis, managing configuration and change control, driving system integration and root-cause analysis, and supporting clinical validation.…See more The role requires 10+ years of industry experience with demonstrated mastery of the full product development lifecycle in medical device or regulated environments, including risk management, design reviews, and cross-functional collaboration with development, testing, and clinical teams.