Jobs at Dexcom

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.

Sr Staff Endpoint Systems Engineer role responsible for designing, standardizing, and managing corporate, R&D, and manufacturing endpoints across Windows and macOS platforms at enterprise scale. The role owns technical direction for endpoint architecture, leads complex projects, and serves as the senior escalation point for endpoint issues and architectural decisions.…See more Key responsibilities include defining endpoint standards, designing secure and scalable solutions using Intune, MECM, and Jamf, developing automation and Infrastructure-as-Code initiatives, and mentoring senior engineers. The ideal candidate is a hands-on expert in PowerShell, Bash, and Python with proven ability to drive automation initiatives, strong endpoint security and hardening expertise, and the ability to influence without direct authority.

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.

This Business System Analyst role focuses on designing, developing, and maintaining reports, dashboards, and analytics solutions within IBM Maximo environments using tools like BIRT, Cognos, Power BI, and MAS Reporting. The analyst will partner with business stakeholders to gather requirements, support Enterprise Asset Management processes, and translate business needs into actionable reporting solutions.…See more Key responsibilities include leading Maximo 2.0 training initiatives, providing functional support and troubleshooting, validating data integrity, and collaborating on system enhancements. The role requires 3–5 years of experience supporting Maximo as a functional or reporting analyst, with strong skills in requirements gathering, SQL, and reporting tool proficiency.

Lead a team of Quality Engineers supporting high-volume manufacturing automation, product introductions, and process validation across multiple programs and sites at a regulated medical-device company. Establish strategic direction for quality engineering, Design Control, Design Transfer, Process Validation, and Manufacturing Quality activities while partnering with Engineering, Operations, and R&D to identify and mitigate risks.…See more Drive continuous improvement through quality metrics, CAPA effectiveness, and nonconformance management, and represent Quality Engineering during audits and regulatory inspections. Manage departmental resources, budgets, and staffing while building and developing high-performing teams.

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.

Sr Staff QA Engineer at Dexcom leads Design Quality Engineering for material characterization, formulation science, and material-related risk management across product development and lifecycle management. The role requires deep expertise in characterizing complex material systems (polymers, enzymes, reagents, adhesives, coatings, membranes) and establishing traceability between material attributes, manufacturing processes, and finished device safety/performance.…See more Responsibilities include driving risk-based decision making using ISO 14971, overseeing qualification strategies, partnering with R&D and regulatory teams, and representing Design Quality in design reviews, audits, and regulatory submissions. Requires 8+ years in medical device, pharmaceutical, or biotechnology quality engineering with demonstrated experience in material characterization and design control processes.

As a Sr SW Test Development Engineer, you will develop and execute test scripts and validations for Dexcom's CGM (continuous glucose monitoring) transmitters and receivers, focusing on BLE (Bluetooth Low Energy) interface testing, interoperability evaluation, and system-level use cases. You'll use Python, Android Debug Bridge (ADB), Ellisys, Selenium, and Appium to create functional and stability tests, debug customer-reported issues, and analyze results to inform next-generation device improvements.…See more The role requires 7–12 years of industry experience with at least 2–4 years in firmware/embedded testing, strong Python scripting skills, and familiarity with embedded protocols (GPIO, UART, SPI, I2C, CAN, TCP/IP, UDP). You'll work in an Agile environment, collaborating cross-functionally and using GitHub, Jira, and Confluence to manage test artifacts and defects.

As a Staff Data Engineer on Dexcom's Commercial Data Science & Revenue Operations team, you will design and operate the company's commercial data platform on AWS, building pipelines that ingest from 12+ vendor sources, transform data, and deliver analytics-ready datasets to data scientists, analysts, and 300+ field representatives. You will own AWS-native development using Lambda, Glue, CDK, Step Functions, and Redshift, with responsibility for data quality frameworks, alerting systems, warehouse schema design, and governance compliance.…See more The role requires hands-on proficiency in Python, SQL, AWS architectures, and CI/CD practices, along with experience building observability infrastructure and working with healthcare compliance requirements like HIPAA. You will also mentor team members and partner with business stakeholders to translate data capabilities into strategy.

Lead complex medical device development programs for Dexcom's Stelo wearable glucose biosensor platform, driving cross-functional teams through research, verification, validation, and commercialization. Direct R&D, commercial, operations, quality, clinical, regulatory, and legal stakeholders; manage product roadmaps, timelines, and executive governance; resolve technical and business tradeoffs while mentoring team members.…See more Requires proven experience shipping novel wearable or connected medical devices with expertise across mechanical, electrical, systems, and mobile app engineering disciplines, plus familiarity with FDA and EU MDR regulatory pathways.

Senior software engineer focused on building cloud-based backend services and data platforms for medical device systems at Dexcom. Design and develop end-to-end data pipelines supporting large-scale ingestion, transformation, and storage, while building and maintaining APIs that expose data to internal systems, partners, and mobile apps.…See more Collaborate with Data Engineers, AI/ML Engineers, and Platform teams to integrate AI insights into production systems, ensuring high standards for reliability, performance, scalability, and data quality. Lead through code reviews, design mentorship, and technical guidance while contributing to architecture decisions and long-term platform roadmap.

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.

This Software Design QA Engineer role focuses on ensuring software development conformance to FDA, IEC 62304, and ISO 13485 standards in a medical device company. The engineer will lead design assurance activities including risk management (SHA, design FMEA), design control reviews, configuration management, and post-market compliance support.…See more The role requires expertise in medical device software development lifecycle processes, regulatory frameworks, and cross-functional collaboration with engineering, test, and regulatory teams.

As Senior Staff Quality Engineer at Dexcom, you will drive quality compliance and inspection readiness across products, processes, and systems in a medical device environment. You'll lead complex investigations, implement corrective and preventive actions, mentor engineers, and ensure adherence to FDA 21 CFR 820 and ISO 13485 requirements.…See more The role requires hands-on expertise in QMS frameworks, design control, regulatory inspections, and the ability to influence stakeholders across engineering, operations, and global sites to maintain continuous audit readiness.

Lead the Sensor Technology workstream for Dexcom's Innovation, Ventures & Sensor Technology PMO, managing biosensing technology development from concept through product lifecycle. Own integrated program timelines, Work Breakdown Structure, and design controls compliance under 21 CFR 820 regulations.…See more Manage budget, resources, risk, documentation in the PLM system, and coordinate build/test activities while serving as the primary stakeholder liaison. This role requires significant medical device development expertise, strong project management skills across waterfall and hybrid methodologies, and preferably a technical background in Material Science or Electrochemistry.

Staff Engineer responsible for developing and implementing scalable engineering systems, processes, and operating models to improve collaboration between product development and operations. The role requires applying robust engineering methodologies (DFM, DFA, DOE, DFSS, Lean Product Development) and systems thinking to solve complex organizational challenges while driving continuous improvement and manufacturing readiness.…See more Success demands the ability to influence cross-functional teams without direct authority, use data-driven decision-making, and coach others to build organizational capability across technical and business functions.

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.

The SW Test Development Engineer 2 will design, develop, and maintain automated and manual test scripts for Dexcom's CGM software and data platform systems. You'll write API and UI tests, create verification and validation test plans, analyze failures with development teams, and contribute to release improvements.…See more The role requires 2–5 years of hands-on software or test development experience with Python or OOP languages, SQL/NoSQL databases, API testing frameworks (Robot framework), and cloud platforms (GCP/AWS); additional experience with Docker, Kubernetes, Kafka, BigQuery, and Airflow is highly valued. You'll mentor junior engineers and work cross-functionally in an Agile environment.

As a SW Test Development Engineer 2 at Dexcom, you will design, develop, and maintain automated and manual test scripts for CGM software systems, including API and UI testing. You will create verification and validation test plans, traceability matrices, and track issues while collaborating with development teams on root cause analysis.…See more The role requires 2–5 years of hands-on software test development experience with Python or other OOP languages, SQL/NoSQL databases, API testing frameworks (including Robot Framework), and cloud platforms (GCP/AWS). You will also mentor junior engineers and contribute to release process improvements.

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.

Staff Technical Program Manager leading early-stage technology development projects within Dexcom's Innovation Ventures & Sensor Technology group. Oversees complex, cross-functional projects from concept through productization, managing project schedules, regulatory compliance, and technology risks while coordinating internal and external stakeholders.…See more Requires strong technical background in biomedical engineering, chemistry, or materials science with medical device development experience, particularly in sensor and algorithm development.

The Maximo Business Analyst & Reporting Analyst supports and optimizes IBM Maximo solutions through business process analysis, reporting development, user training, and functional support. The role serves as liaison between business stakeholders and technical teams, driving Maximo 2.0 adoption through training programs while developing enterprise reporting solutions.…See more Key responsibilities include gathering business requirements, designing reports and dashboards across multiple platforms, leading end-user training initiatives, and providing functional support for Maximo-related issues. The position requires 3–5 years of experience with IBM Maximo and proficiency in reporting tools such as BIRT, Cognos, Power BI, or MAS Reporting.

As a SW Test Development Engineer 2, you will design and build automation tools and frameworks to test Dexcom's continuous glucose monitoring devices and mobile apps (iOS/Android). You will develop in Python or Java to create testing APIs, integrate tools like Jira, Testrail, Slack, and GitHub, and manage end-to-end test suites in CI/CD pipelines.…See more The role requires 2–3 years of software development experience with object-oriented languages, hands-on familiarity with cloud platforms (AWS/GCP), containerization (Docker), and embedded/mobile device automation.