design-of-experiments jobs in San Diego

As a Development Sr Engineer II, you will serve as a design owner and project manager for new medical device product design, development, and commercialization in the orthopedic/arthroplasty space. You will translate user needs from surgeons into design requirements, create CAD models and design documentation, conduct design verification/validation testing, and support regulatory and manufacturing teams through product launch.…See more The role demands expertise in parametric CAD modeling, finite element analysis, design of experiments, and medical device regulations and standards.

Senior Automation Engineer responsible for investigating equipment and process performance, optimizing designs and fixture systems, and managing capital planning for automation investments. Will lead end-to-end automation projects from requirements through FAT/SAT/deployment, specify and qualify manufacturing equipment, and drive the transfer of processes from R&D to production at scale.…See more Requires 8–12 years' experience in automated manufacturing systems, design of experiments, statistical analysis, and regulatory compliance (FDA 21 CFR Part 820, ISO 13485), with hands-on expertise in PLC/HMI, robotics, machine vision, and equipment integration.

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.

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.

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.…See more 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.

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.

Test Engineer II will design, set up, and execute fluidic and electrochemistry experiments in a hands-on laboratory setting, owning test plans from definition through data analysis. Responsibilities include programming and configuring automated test instrumentation, assembling and characterizing prototype consumables and fluidic sub-assemblies, and performing root cause investigations and design-of-experiments (DOE) to resolve hardware and process issues.…See more The role requires 2–4 years of hands-on R&D laboratory experience with fluidic-based systems, experimental design, and troubleshooting. Programming experience (MATLAB, LabVIEW, C++, Python) and familiarity with metrology, microfluidics, or molecular diagnostics platforms are preferred.