six-sigma jobs in San Diego

Sr QA Engineer leading complex quality investigations, root cause analysis, CAPAs, and NCMRs at a regulated medical device company (Dexcom). Drives Quality Management System excellence through continuous improvement methodologies (Six Sigma, Lean, process capability analysis), owns validation and qualification strategies for equipment/processes/software, and guides design transfer and commercialization from development to high-volume manufacturing.…See more Requires advanced quality engineering knowledge, hands-on technical aptitude, proficiency with data analysis tools (JMP, Excel), and cross-functional leadership across R&D, Regulatory, Manufacturing, and Engineering teams.

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.

This role leads quality engineering strategy and operations for a medical device design center, overseeing compliance with FDA regulations (21 CFR 820, ISO 13485, ISO 14971) and managing a team of Quality Engineers. The manager develops and sustains quality management systems, executes quality initiatives, provides statistical and design-control expertise, and drives continuous improvement.…See more The position requires ten years of progressive QA experience in FDA-regulated industries, three years of direct management experience, and deep knowledge of design controls, risk management, and quality engineering methodologies.

Staff Quality Analyst role responsible for building dashboards and analytics that surface defect signals and drive leadership decision-making at scale. The role combines hands-on data analysis (SQL, Python, statistics) with AI-native workflows to accelerate defect detection and root cause analysis, plus structured change management to land measurement and process changes across large stakeholder groups.…See more Required skills include strong SQL/Python proficiency, applied statistics, experience with defect frameworks (DPMO), contact center operations familiarity, and demonstrated ability to communicate data findings credibly to executives and manage organizational change.

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.

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.

Lead end-to-end technical program execution for TeraWave Q/V-band RFIC and phased-array antenna developments from requirements through production qualification. Coordinate internal engineering teams across development lifecycle phases, build integrated schedules and risk registers, and drive alignment between IC deliverables and system-level requirements.…See more Manage third-party IP, foundry, and supplier partnerships while fostering cross-functional accountability across RF, systems, packaging, test, and manufacturing teams. Requires 10+ years in technical program management with direct experience managing RF IC programs and ability to credibly lead highly technical semiconductor and communications teams.

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 complex quality investigations and root cause analysis for a medical device company, driving CAPAs, NCMRs, and systemic corrective actions. Provide technical leadership in quality engineering methodologies including Six Sigma, Lean Manufacturing, process capability analysis, and risk-based problem solving.…See more Own validation and qualification strategies for equipment, processes, test methods, and software V&V across the product lifecycle. Partner with R&D, Regulatory Affairs, Manufacturing, and Engineering teams on design transfer, commercialization, and compliance initiatives while representing Quality during audits and regulatory inspections.

Lead Oracle EBS Financials and Oracle Cloud ERP implementations for tax clients, with primary focus on direct tax engines, compliance, and reporting solutions. Design and implement technology solutions addressing corporate tax needs across compliance, reporting, and planning functions.…See more Manage cross-functional teams, mentor staff, and drive business development while maintaining a hybrid work model with 2–3 days per week in-person co-location and up to 50% travel.

Blue Origin seeks a Technical Program Manager to lead SoC (System-on-Chip) development programs from requirements through production. The role requires managing complex hardware and semiconductor programs across multiple lifecycle phases, coordinating with highly technical engineering teams, external suppliers, and IP providers.…See more Responsibilities include change management, build-versus-buy decisions, supplier strategy, scheduling, risk management, and translating between detailed technical execution and business objectives. The ideal candidate has 7+ years of technical program management experience, a strong background in IC/SoC development, analog/mixed-signal design, digital ASIC, RF systems, or satellite communications, plus demonstrated ability to lead through tapeout, silicon bring-up, qualification, and production ramp.

Staff QA Engineer at Dexcom leading manufacturing quality and regulatory compliance for continuous glucose monitoring devices. Responsibilities include directing Design Control and design transfer strategy, managing process validation and commercialization, leading cross-functional teams on complex technical and compliance matters, and providing expert guidance on Quality Management System governance (FMEA, CAPA, process controls).…See more Requires deep hands-on experience with FDA 21 CFR 820, ISO 13485, and related QMS requirements, plus ability to mentor teams and represent the organization during audits and regulatory inspections.

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.