verification-and-validation jobs in San Diego

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.

Senior Systems Engineer responsible for leading system integration planning, verification and validation strategy, and reliability engineering for complex medical devices or integrated systems at BD. Own cross-functional coordination across Reliability, Software, Electrical, Mechanical, Quality, Regulatory, Manufacturing, and Clinical teams while investigating system-level issues, managing technical risks (FMEA, hazard analysis), and mentoring junior engineers.…See more Develop requirements, drive design reviews, and apply Design for Six Sigma (DFSS) methodologies to enhance product quality and development efficiency from concept through commercialization.

The Senior Systems Engineer leads the full lifecycle of compute, camera, and radio systems—from requirements development through design, integration, testing, and qualification. You'll develop system architecture, define interfaces, conduct trade studies, and oversee verification and validation across hardware and software.…See more The role requires 8+ years of systems engineering experience, deep expertise in embedded systems (ARM, PowerPC, x86 processors), flight and ground software, RTOSes, and embedded protocols (SpaceWire, CameraLink, CAN, etc.), plus proficiency in C/C++, Python, and requirements management tools.

Staff Systems Engineer at BD will lead systems engineering efforts across complex medical device programs, driving reliability planning, product quality improvements, and cross-functional technical collaboration. The role requires deep expertise in requirements management, system architecture development, verification/validation, and risk management, with responsibility for mentoring junior systems engineers and championing MBSE and design methodologies.…See more The ideal candidate has 6–8+ years of systems engineering experience, preferably in regulated medical device development, and demonstrates exceptional ability to influence technical strategy across multiple disciplines without direct authority.

Director-level role leading a software engineering team at a life sciences company building multi-omic analysis platforms. Requires hands-on full-stack expertise (React, Go, AWS, Temporal) alongside team management, architecture ownership, and end-to-end product delivery.…See more Must drive regulated software compliance (IEC 62304, ISO 13485, FDA 21 CFR Part 820), design controls, and V&V documentation while prototyping with AI tools and scaling agentic workflows within the team.

Director of Software Engineering leading end-to-end delivery across customer-facing products and internal tooling at a life-sciences company. This role combines hands-on full-stack development (React, Go, AWS, Temporal) with team leadership, architecture ownership, and regulated software compliance (IEC 62304, ISO 13485, FDA 21 CFR Part 820).…See more Candidates should have 10+ years of software engineering with 3+ years managing teams, fluency with modern AI coding assistants, and experience shipping instrumentation, cloud SaaS, and ML/AI features.

This Systems Engineer role at a medical device company requires decomposing regulatory and stakeholder requirements into testable system specifications, leading design reviews and verification/validation activities, and supporting risk management under FDA and ISO frameworks. The position demands 2+ years in a regulated medical device environment, with responsibility for traceability documentation, design history files, failure investigation, and CAPA activities.…See more Key competencies include FDA design controls, ISO 14971 risk management, human factors/usability per FDA guidance, and cross-functional communication of complex system interfaces to diverse audiences.

Associate Test Engineer supporting the Blue Swordfish maritime autonomous platform project. Responsibilities include developing test plans, methods, cases, and procedures; conducting walk-throughs; executing tests on autonomous maritime systems; documenting and analyzing test results; and supporting at-sea testing and demonstrations.…See more Requires a bachelor's degree in computer science, engineering, or related field, U.S. citizenship, ability to obtain a Secret clearance, and hands-on experience with Linux, Java, C++, Python, Agile methodologies, and test/evaluation of complex systems.

Senior Systems Engineer responsible for leading complex space-based systems and payload development, including formal verification and validation activities. The role requires designing, integrating, and testing defense systems while collaborating across engineering disciplines and customer interfaces.…See more You will apply systems engineering principles (V-model, MBSE), develop AI&T plans, manage configuration and change control, and generate technical documentation using digital engineering tools. The position requires 12+ years of engineering experience (or equivalent with advanced degrees), an active Top Secret/SCI clearance, and proven ability to lead integrated product teams on space-qualified hardware programs.

Senior Test Engineer supporting complex Department of Defense systems, responsible for developing, reviewing, and maintaining Test and Evaluation Master Plans, test strategies, procedures, and technical documentation. Coordinate with multiple agencies (OPTEVFOR, JITC, OPNAV) and support laboratory, platform, flight, and operational test events.…See more Lead development of test deliverables, data collection plans, and analysis of test deficiencies, anomalies, and risks. Requires 8+ years of engineering experience on DoD systems with 4+ years in developmental or operational test and evaluation.

Senior Automation Engineer supporting development, maintenance, and operation of complex custom automation systems in a biotech environment. Responsibilities include understanding system requirements, developing scripted protocols, integrating hardware and software components, troubleshooting failures, and ensuring compliance with FDA regulations and GxP principles.…See more Requires 5+ years in hardware design, automation, or biotech, with proficiency in C#, robotics, motion control, machine vision, and electronic systems integration.

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.

Senior Automation Engineer at a biotech firm developing autologous stem-cell therapies. Responsible for developing, maintaining, and troubleshooting complex custom automation systems, including scripted protocols, hardware-software integration, and verification/validation testing.…See more Requires 5+ years in hardware design, automation, or biotech, with strong C# software integration skills, robotics and motion control expertise, and knowledge of FDA regulations (21 CFR 11, 210, 211, 820) and GxP principles.

Lead a systems engineering team responsible for avionics integration, verification, and validation activities for satellite communication systems. Direct technical problem-solving during integration phases, oversee certification and compliance (DO-160 frameworks), manage system architecture decisions across hardware and software, and ensure airworthiness of deployed solutions.…See more Manage team budget, conduct performance reviews, and serve as technical spokesperson to internal/external stakeholders. Required skills include 7+ years in avionics/aerospace systems engineering with hands-on experience in embedded Linux/Windows, avionics I/O interfaces (ARINC 429, CAN, Ethernet), IVV tooling (git, Jira, bash, Python), and lab test equipment.

The Senior Automation Engineer will develop, maintain, and troubleshoot complex custom automation systems in a biotech setting, working with hardware (robotics, motion platforms, sensors, machine vision) and software (C# codebases). Responsibilities include creating operational protocols, supporting system integration, developing verification and validation plans, and ensuring compliance with FDA regulations (21 CFR Parts 11, 210, 211, 820) and GxP principles.…See more The role requires 5+ years in hardware design, automation, or biotechnology, with strong problem-solving skills and the ability to collaborate across cross-functional teams.

The Senior Design Quality Engineer ensures digital health products comply with FDA regulations, quality standards, and user requirements through design controls and verification/validation activities. They manage digital health projects from concept to production using phase-gate approaches, lead or support CAPAs and NCRs, conduct internal/external audits, and apply risk management throughout the design lifecycle.…See more The role requires advanced knowledge of FDA design controls and IEC 62304 software standards, with hands-on experience taking products through regulatory compliance. The engineer will work independently, provide executive guidance on quality matters, and serve as a best-practice resource within their area of expertise.

Systems Engineer supporting U.S. Navy command and control programs under Naval Information Warfare Systems Command (NAVWAR), responsible for maritime surveillance and C2 capability integration for partner nations.…See more Core duties include requirements definition and traceability, system-of-systems architecture across dissimilar systems, interface definition and control, test/verification/validation planning, technical trade studies, and coordination across multiple program offices. The role demands hands-on systems engineering discipline: turning partner-nation requirements into defined interfaces, integrating capabilities never designed to interoperate, and verifying results meet specifications. Must be comfortable with computing and network environments (LAN/WAN, TCP/IP, routing, switching, Windows/Linux servers, virtualization) sufficient to troubleshoot credibly alongside network engineers.

Lead software development for an FDA-cleared blood testing platform, overseeing instrument software, application software, cloud connectivity, cybersecurity, and software quality systems. Manage the full software development lifecycle including requirements, risk management, design controls, verification and validation, and regulatory compliance.…See more Work closely with Quality and Regulatory Affairs on FDA submissions, audits, documentation, and post-market support. Direct strategy, roadmap planning, architecture, and release management for a regulated in vitro diagnostic (IVD) medical device.

Lead a team of firmware validation engineers responsible for defining and executing verification and validation strategy for Zoox's software core systems. Direct testing efforts targeting bootloaders, device drivers, networking stacks, operating systems, C++ frameworks, middleware, and system services running on POSIX and non-POSIX real-time operating systems.…See more Collaborate with firmware, software, release management, and vehicle engineering teams to develop industry-best testing methodologies with a focus on safety assurance and reliability.