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Talent Development & Executive Engagement: Coach and manage 1–2 aligned professionals; actively contribute to a Community of Practice; support QBRs and produce executive-ready readouts.

Dexcom

QA Engineer 2

Mesa, United States

$71,600.00 - $119,300.00

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Job details

Pay: $71,600.00 - $119,300.00
Apply by: May 8, 2027
Experience: Typically requires a Bachelor’s degree in a technical discipline and 2–5 years of related experience, or a Master’s degree and 0–2 years of equivalent industry experience.
Posting language: English
Posted: Nov 9, 2026

Original job description

Meet the team:

Our Quality organization is the backbone of Dexcom - ensuring that every product released to patients meets the highest standards of safety, reliability, and regulatory compliance. As a cross‑functional partner to Operations, R&D, Regulatory, and Manufacturing, the Quality team drives a culture of excellence by embedding robust processes, rigorous risk management, and continuous improvement into every stage of the product lifecycle. Their work safeguards patient outcomes, protects the integrity of the business, and reinforces trust with clinicians, regulators, and customers worldwide.

At the center of this mission, the Quality Engineer II plays a critical technical and leadership role. Operating as both a subject‑matter expert and strategic problem‑solver, the Quality Engineer leads complex investigations, develops and strengthens quality systems, influences product and process design, and drives data‑driven decision making across the organization. They mentor engineers, shape best practices, elevate risk‑based thinking, and ensure that manufacturing and design teams consistently deliver products that meet stringent regulatory and performance requirements. In essence, the Quality Engineer is a key architect of quality - bridging technical depth with cross‑functional leadership to ensure safe, effective, and compliant medical devices reach patients who depend on them.

Where you come in:

You will implement and maintain quality assurance protocols and methods for processing materials into partially finished or finished products.
You will ensure compliance to in-house and/or external specifications and standards (i.e. GLP, GMP, ISO, Six Sigma).
You will complete investigations into nonconformances
You will assist in high‑visibility quality engineering projects with cross‑functional teams
You will assist in identifying systemic issues and drive long‑term corrective and preventive actions

What makes you successful:

You will need an understanding of FDA QSR, ISO 13485, and risk‑management requirements.
Your knowledge in statistical tools, root cause analysis, validation, and problem‑solving methodologies.
Your communication skills, capable of presenting complex information clearly to technical and non‑technical audiences.
Your ability to thrive in a fast‑paced environment and manage multiple priorities.
Your passion for developing others and lifting team performance through coaching and example.

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 2–5 years of related experience, or a Master’s degree and 0–2 years of equivalent industry experience.

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 talentacquisition@dexcom.com.

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 talentacquisition@dexcom.com.

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

AI in Hiring Notice: We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people.

Salary:

$71,600.00 - $119,300.00

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More about this job

Skills

Decision making
Quality assurance
Regulatory compliance
Good laboratory practices
Good manufacturing practices
Lean manufacturing
Risk management
Root cause analysis
Problem solving
Communication skills
Coaching
Microsoft Access
Recruitment

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