Supplier Quality Technician 4, Athenry

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 and to unlock information and insights that drive better health outcomes. We are broadening our vision beyond diabetes to empower people to take control of health with personalized, actionable insights. This role contributes to improving human health on a global scale.

Meet The Team The incumbent is responsible for performing the duties of a Supplier Quality Technician, with moderate oversight from the manager and/or senior level supplier QEs.

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

6–8 years of experience in a medical device or similarly regulated manufacturing environment.

Strong shop‑floor presence and ownership of assigned quality systems, proactively engaging with Operations to support compliance and real‑time issue resolution.

Active participation in nonconformance investigations and CAPA activities through timely assessment, effective collaboration, and thorough documentation.

Audit‑ready behaviours with a clear understanding of FDA, ISO, and MDSAP requirements, and the ability to support inspections and audits confidently.

Sound judgement and confident decision‑making, taking ownership of issues while knowing when and how to appropriately elevate them.

Ability to work 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.

A full and comprehensive benefits program.

Growth opportunities on a global scale.

Access to career development through in‑house learning programs and/or tuition reimbursement.

An exciting and innovative, industry‑leading organization committed to our employees, customers, and the communities we serve.

Travel Required

15‑25% travel to the U.S. and internationally.

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