Hardware Engineer 2

Dexcom; California (MO); Hybrid; USD 91,000 - 152,000; Full time

Benefits offered by this job

Comprehensive benefits

Global growth opportunities

Career development

Job summary

Dexcom is seeking a Postmarket Investigations professional to support the Customer Advocacy organization. You will collaborate with Regulatory Affairs, Quality Assurance, R&D, Clinical, and Process Engineering to investigate software- and device-related postmarket issues.

You will lead structured problem‑solving, perform risk assessments, and translate insights into product improvements while ensuring patient safety and regulatory compliance.

Qualifications

• Knowledge of medical device quality systems and regulatory requirements (FDA 21 CFR Part 820, ISO 13485, ISO 14971, EU MDR).
• Experience with hardware quality and reliability activities across product lifecycle.
• Strong analytical mindset with data interpretation and trend identification.

Responsibilities

• Collaborate with Regulatory Affairs, Quality Assurance, R&D, Clinical, and Process Engineering to investigate and resolve postmarket issues.
• Drive development and continuous improvement of complaint investigation processes aligned with risk management activities.
• Develop deep understanding of Dexcom’s hardware ecosystem to evaluate performance and identify improvement opportunities.
• Apply structured problem-solving and data-driven approaches to lead investigations and identify root causes.
• Communicate investigation outcomes to stakeholders and support informed decision-making across the organization.
• Contribute to postmarket quality processes (CAPA, HHEs) and risk assessments.
• Perform hardware-focused risk assessments related to product anomalies and clinical impact.
• Translate postmarket insights into actionable improvements with product development and quality teams.

Skills

Postmarket investigations

Regulatory compliance

Hardware quality

Risk management

Data analysis

Cross‑functional collaboration

Education

Bachelor’s degree in a technical discipline

Tools

Statistical analysis tools

Job description

The Company

Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.

We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing‑technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.

Meet The Team

At Dexcom, the Postmarket Investigations team serves as a critical link between real‑world product performance and continuous product improvement. As part of the Customer Advocacy organization, we assess postmarket feedback and product data to ensure learnings are integrated into future product enhancements. This role has a direct impact on patient safety, product reliability, and regulatory compliance through partnership with teams across R&D, Quality, and Commercial Operations. Our team values technical excellence, accountability, and continuous learning, while fostering a collaborative and supportive environment. Team members have the unique opportunity to drive quality improvements, influence key business processes, and contribute to technologies that empower people to take control of their health.

Where You Come In

• You will collaborate with cross‑functional partners including Regulatory Affairs, Quality Assurance, R&D, Clinical, and Process Engineering to support the investigation, documentation, and resolution of software‑ and device‑related postmarket issues.
• You will drive the development and continuous improvement of complaint investigation processes, ensuring alignment with software risk management activities such as hazard analysis, DFMEA, PFMEA, and product risk assessments.
• You will develop and maintain a deep understanding of Dexcom’s hardware ecosystem to effectively evaluate product performance, investigate anomalies, and identify opportunities for continuous improvement.
• You will apply structured problem‑solving methodologies and data‑driven approaches to conduct investigations, lead engineering studies, and identify root causes using statistical analysis and industry‑standard tools.
• You will analyze, synthesize, and communicate investigation outcomes to technical and non‑technical stakeholders, providing clear recommendations and supporting informed decision‑making across the organization.
• You will contribute to postmarket quality processes, including CAPA, Health Hazard Evaluations (HHEs), and other quality system activities, ensuring thorough assessment of product performance and risk.
• You will perform hardware‑focused risk assessments related to product anomalies, clinical impact, emerging technologies, and postmarket trends, helping to ensure product safety, reliability, and regulatory compliance.
• You will partner with product development and quality teams to translate postmarket insights into actionable improvements, driving enhancements to product performance, user experience, and patient safety.

What Makes You Successful

• You have demonstrated knowledge of medical device quality systems and regulatory requirements, including FDA 21 CFR Part 820, ISO 13485, ISO 14971, EU MDR, and other applicable global regulations, with a strong understanding of postmarket surveillance, complaint handling, CAPA, and vigilance reporting requirements.
• You have experience supporting hardware quality and reliability activities throughout the product lifecycle, including design and development, verification and validation, field performance monitoring, and postmarket surveillance.
• You have strong understanding of hardware risk management principles and methodologies, with the ability to evaluate and mitigate product risks, assess field safety signals, and apply risk‑based decision‑making in alignment with regulatory expectations and industry best practices.
• You have excellent communication and collaboration skills, with the ability to effectively convey complex technical concepts to both technical and non‑technical stakeholders across the organization.
• You have working knowledge of hardware engineering principles and technologies, including electromechanical systems, electronics, sensors, materials, reliability engineering, manufacturing processes, and failure analysis techniques used in medical device development and support.
• You have proven ability to apply engineering fundamentals and structured problem‑solving techniques to investigate complex issues, determine root causes, and drive effective corrective actions.
• You have strong analytical mindset with experience interpreting data, identifying trends, and translating findings into actionable recommendations.
• You have the ability to balance technical depth with business impact, driving decisions that support product quality, patient safety, compliance, and customer experience.
• You have experience performing postmarket surveillance activities, including complaint investigations, trending and signal detection, reliability analysis, risk assessments, CAPA support, periodic product reviews, and communication of field performance insights to internal and external stakeholders.

What You’ll Get

• A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
• A full and comprehensive benefits program.
• Growth opportunities on a global scale.
• Access to career development through in‑house learning programs and/or qualified tuition reimbursement.
• An exciting and innovative, industry‑leading organization committed to our employees, customers, and the communities we serve.

Travel Required

• 0‑5%

Experience And Education Requirements

• Typically requires a Bachelor’s degree in a technical discipline, and a minimum of 2 ‑ 5 years related experience or Master’s degree and 0‑2 years' equivalent experience.

Flex Workplace

Your primary location will be a home office. You will not have an assigned workstation and will work with your manager to determine office visit needs. You must live within commuting distance of your assigned Dexcom site (typically 75 miles/120km).

Please note: The information contained herein is not intended to be an all‑inclusive list of the duties and responsibilities of the job, nor are they intended to be an all‑inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at [e-mail].

If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at [e-mail].

Meritain, an Aetna Company, creates and publishes the Machine‑Readable Files on behalf of Dexcom. To link to the Machine‑Readable Files, please click on the URL provided: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true

To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

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Salary

$91,400.00 - $152,300.00

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