Supplier Quality Technician 4

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:

The incumbent is responsible for performing the duties of a Supplier Quality Technician, as stated in this job description. Performs tasks with moderate oversight from the manager and/or designated senior level supplier QEs.

Will assist supplier quality engineers in the performance of their duties and will support, evaluate, revise and implement specific aspects of the quality system, as assigned.

The incumbent will be systematic, highly organized and articulate, and work well in a team environment. Also to be proficient computer skills in the use of Microsoft Office and database applications (such as Oracle and Agile).

 Job tasks require interfacing with external suppliers, internal manufacturing, engineering, regulatory, quality, materials, operations personnel and senior management.

A positive attitude is important while working in a fast-paced manufacturing environment and dealing with shifting priorities.

Where you come in:

• You will support Supplier Quality Engineering activities including Change Orders, NCEs, NCMRs, SCAR, CAPA investigations, and the assessment and disposition of nonconforming materials with cross‑functional teams.
• You will collect manufacturing and inspection data, perform inspections, and support quality investigations led by Engineers.
• You will Provide day‑to‑day quality support on the manufacturing floor, assisting production and inspection teams with methods, processes, specifications, and quality issues.
• You will ensure compliance with internal quality systems and external regulations and standards (GMP, GLP, ISO, Six Sigma) to enable safe, compliant global product distribution.
• You will Maintain and update quality procedures, protocols, and methods; perform routine line audits to verify systems are effective and operating as intended.
• You will identify and contribute to quality and process improvement initiatives, support corrective actions, and communicate concerns related to quality, safety, health, or environmental impact.
• You will demonstrate strong documentation practices, attention to detail, sound decision‑making, and independent working ability; interpret drawings and specifications, use inspection tools and Microsoft Office effectively, and support training of junior staff as needed.

What makes you successful:

• You will demonstrate 6–8 years of experience working effectively in a medical device or similarly regulated manufacturing environment, applying quality systems with confidence and consistency.
• You will show strong shop‑floor presence and ownership of assigned quality systems, proactively engaging with Operations to support compliance and real‑time issue resolution.
• You will actively contribute to nonconformance investigations and CAPA activities through timely assessment, effective collaboration, and thorough documentation.
• You will maintain audit‑ready behaviours at all times, with a clear understanding of FDA, ISO, and MDSAP requirements and the ability to support inspections and audits confidently.
• You will demonstrate sound judgement and confident decision‑making, taking ownership of issues while knowing when and how to escalate appropriately.
• You will work effectively both independently with minimal supervision and collaboratively within cross‑functional teams to achieve quality and operational objectives.

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:

• 15-25% - Ability to travel to the U.S. and internationally.

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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