statistical-analysis jobs in San Diego

As an AI and Data Science Engineer III, you will translate business goals into machine learning use cases and develop predictive models for marketing and advertising applications. You'll perform exploratory data analysis, apply clustering and feature transformation techniques, build proofs of concept, and validate solutions.…See more The role requires 5+ years of industry experience applying data science or machine learning methods, with a strong foundation in translating business requirements into model design approaches and collaborating across analytics and data engineering teams.

This role supports neuroimaging research by performing manual image review and quality assurance on MRI data, conducting statistical analyses using MATLAB and Python, and maintaining data integrity across multiple acquisition sites. The analyst will design and implement data analysis tools, configure pipelines, write shell scripts and standard operating procedures, and troubleshoot data quality issues in coordination with partner institutions.…See more The position requires proficiency in Linux, shell scripting, MATLAB, and Python, along with hands-on experience analyzing structural and functional MRI neuroanatomic data and applying bioinformatics QC methods.

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.

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.

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.

Lead a team of data scientists at Insulet's Analytics Center of Excellence, managing the execution of global analytics and AI initiatives while maintaining hands-on expertise in data science work. You will mentor scientists, guide development of cloud-based analytics pipelines and automated machine learning solutions, and coordinate with cross-functional stakeholders across R&D, clinical, quality, and manufacturing to identify and deliver high-value data science opportunities.…See more The role requires a Master's degree with 5+ years in data science (or PhD with 3+), 2+ years in machine learning/AI, direct team management experience, and proficiency in Python/R, SQL, cloud platforms (Azure/AWS/GCP), and big data technologies like Spark/Databricks. You'll perform statistical analysis, predictive modeling, and communicate insights to executives while owning the data products portfolio and managing annual budgets.

This role supports the full product lifecycle for complex integrated systems, focusing on requirements management, system integration, verification & validation, and risk management. The Systems Engineer will conduct FMEA and hazard analysis, collaborate across software, electrical, mechanical, quality, and regulatory teams, and drive activities from concept through launch.…See more The position requires 3+ years of systems engineering experience, a bachelor's degree in engineering, and expertise in requirements traceability and risk assessment.

Quality Assurance Engineer responsible for implementing, maintaining, and improving quality management systems (ISO 9001, ISO 14001, ISO 13485, AS9100, Nadcap) in a manufacturing environment. The role involves developing work instructions, managing compliance documentation, conducting customer audits, and driving corrective action initiatives.…See more Requires 2+ years manufacturing experience (or 6+ years without a degree), proficiency with statistical analysis software, SAP, and the ability to interpret engineering drawings and GD&T. May supervise QA technicians and must be eligible to work in an ITAR environment.

As a Senior Software QA Engineer at Dexcom, you will investigate postmarket software and device issues in collaboration with Regulatory, Quality, R&D, and Clinical teams, applying structured problem-solving and statistical analysis to identify root causes and drive corrective actions. You will develop and improve complaint investigation processes aligned with software risk management activities (hazard analysis, DFMEA, PFMEA, risk assessments) and ensure compliance with FDA 21 CFR Part 820, IEC 62304, ISO 13485, ISO 14971, and other medical device regulations.…See more You will analyze product performance anomalies, cybersecurity vulnerabilities, and postmarket trends to conduct software-focused risk assessments, then communicate findings and recommendations to technical and non-technical stakeholders to inform decision-making. You will translate postmarket insights into actionable product improvements that enhance safety, reliability, user experience, and regulatory compliance.

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.

Software Engineer at Leidos' Undersea Systems Division developing and testing uncrewed underwater vehicles (UUVs) for Naval Information Warfare Center, Pacific. Responsibilities include UUV operations software, sensor integration and control, behavior optimization, and platform-independent data processing tools.…See more Requires strong systems programming in Linux, Python, and C/C++; practical TCP networking and socket-level data transport; ROS2, CAN bus, UDP, and telemetry analysis experience. Role includes hands-on hardware/software bring-up, benchtop troubleshooting, sea-based testing, and occasional travel.

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 Product Surveillance Engineer responsible for investigating postmarket software and device issues, driving complaint investigation processes, and ensuring regulatory compliance for medical devices. The role requires deep understanding of Dexcom's software architecture to evaluate product performance, apply structured problem-solving and statistical analysis to root-cause investigations, and communicate findings to technical and non-technical stakeholders.…See more You will support quality system activities (CAPA, HHEs), conduct software risk assessments, and partner with product and quality teams to translate postmarket insights into product improvements. Success requires demonstrated knowledge of FDA 21 CFR Part 820, IEC 62304, ISO 13485, ISO 14971, and medical device quality systems.

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 Staff QA Engineer at Dexcom leading Design Quality Engineering for material characterization, formulation science, and material-related risk management across product lifecycle. Responsibilities include establishing traceability between material attributes and device performance, leading qualification strategies for polymers, enzymes, reagents, adhesives, coatings, and membranes, applying ISO 14971 risk management, and partnering with R&D, Materials Science, Analytical Chemistry, Process Development, Manufacturing, and Regulatory Affairs.…See more Requires 8+ years in medical device, pharmaceutical, biotechnology, or combination product development with deep expertise in material characterization, analytical chemistry, and formulation development.

Associate Systems Engineer supporting the development and enhancement of in-vitro diagnostic (IVD) instruments within a regulated medical device environment. The role involves system integration testing, verification and validation (V&V) activities, troubleshooting, failure investigations, and risk assessments across multiple R&D projects.…See more Responsibilities include executing statistical analyses, performing root cause analysis, contributing to design control documentation and regulatory submissions, and collaborating with cross-functional teams (software, hardware, assay development, quality, manufacturing). Requires a Bachelor's degree in Systems Engineering, Bioengineering, Mechanical Engineering, Electrical Engineering, or related field with 0–3 years of relevant experience; Master's preferred.

Support system-level verification planning, coordination, and execution for medical device product development and sustaining engineering projects. Translate customer needs into testable requirements, participate in risk assessments and design reviews, and collaborate across engineering disciplines to resolve technical issues.…See more Apply Design for Six Sigma (DFSS) principles and quality engineering practices throughout the product lifecycle. Requires a bachelor's degree in engineering or related field and 1–2+ years of product testing, design verification, systems engineering, or quality engineering experience.

Systems Engineer II supporting system-level verification planning, execution, and documentation for medical device product development and sustaining engineering projects. The role requires translating customer needs into testable requirements, developing verification protocols and traceability documentation, conducting risk assessments and hazard analyses, and collaborating across engineering disciplines.…See more Requires a Bachelor's degree in Engineering or related field plus 1-2+ years of relevant engineering experience in product testing, design verification, systems engineering, or quality engineering, with strong analytical, technical writing, and cross-functional collaboration skills.

Quality Assurance Specialist II leads and supports audit activities, serves as a QA subject matter expert during inspections, and manages quality events and risk assessments for medical device products. The role involves conducting root cause analyses, managing document control and training workflows, coordinating the internal audit program, and driving quality-system improvement projects.…See more The position requires a bachelor's degree in a scientific or engineering discipline with 3–5 years of QA or regulatory affairs experience in a regulated industry, with medical device experience highly preferred. Key responsibilities include compliance with ISO 13485 and 21 CFR Part 820, partnership with senior quality engineers on risk management, and eQMS implementation and validation.

As a Senior Data Scientist on PlayStation's Decision Science team, you will lead the design, execution, and interpretation of A/B tests and quasi-experiments to evaluate PS4-to-PS5 migration initiatives, growth marketing strategies, and campaign performance. You'll apply advanced causal inference methods, develop experimentation frameworks and best practices, and independently extract and analyze data using SQL and Python.…See more The role requires deep expertise in experimental design, statistical rigor, and the ability to communicate findings to drive business decisions across product, engineering, and marketing teams.

Staff Reliability Engineer to lead reliability strategy for Qualcomm's data center products, owning reliability planning, advanced analysis (device aging, electromigration, wear-out modeling), and qualification test architecture (HTOL, bHAST/THB, ESD/LU). The role requires performing statistical failure-rate modeling, driving design-for-reliability improvements across cross-functional teams, and mentoring junior engineers to establish best practices.…See more Requires 4+ years of reliability engineering experience with expertise in JEDEC standards, silicon process technology, advanced packaging (chiplets, 2.5D/3D integration), and complex Digital SoC qualification.

Lead large-dataset analysis projects for lending clients, cleaning and analyzing millions of loan-origination records while maintaining rigorous data quality and defensible methodology. Design analyses around customer business goals, translate findings into clear ROI narratives for both technical and executive audiences, and present results directly to stakeholders.…See more Build reusable queries, templates, and documentation to improve study consistency and speed. Spend 20% of time supporting sales through discovery calls, product demos, and creating sales materials.

This Systems Integration Engineer II/III role centers on hands-on system validation, verification, and reliability testing for complex life-science instrumentation integrating hardware, software, firmware, optics, lasers, fluidics, and motion control. The engineer will conduct cross-functional troubleshooting, execute structured test protocols, analyze instrument performance data using statistical methods and Python, and document findings to drive design improvements and field support readiness.…See more Key responsibilities include evaluating workflows against real customer use cases, performing root-cause analysis on failure modes, and continuously refining integration documentation and testing practices. The role requires 2–5 years of systems integration or testing experience, proficiency in DOE/FMEA/statistical analysis, and hands-on lab work with prototypes and integrated instruments.

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.

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.