Front-End Quality Technician – Day Shift (12-hr)

Dexcom Inc.; Athenry; On-site; EUR 37,000 - 48,000; Full time

Job summary

Dexcom Ireland is hiring a Quality Technician to support Quality Control and Quality Assurance in a GMP‑regulated medical device manufacturing environment. You will assist with nonconformance events, audits, and QA/QC documentation while collaborating with cross‑functional teams to ensure product quality and regulatory compliance.

The role emphasizes on‑floor presence, adherence to ISO 13485 and FDA/ISO standards, and ongoing process improvements across the site.

Qualifications

• 2–4 years of experience in a medical device or similarly regulated manufacturing environment.
• Strong shop-floor presence and ownership of quality systems.
• Experience with FDA, ISO, and MDSAP requirements and audits.
• Knowledge of ISO 13485, 21 CFR Part 11, 21 CFR 820, and related manufacturing systems.

Responsibilities

• Support Quality Engineering activities including Change Order processing, Nonconformance Events, Nonconforming Material Reports, and CAPA investigations.
• Collect manufacturing and inspection data and perform inspections to support investigations.
• Assist the inspection team with questions related to inspection methods, processes, and specifications.
• Ensure compliance with GMP, GLP, ISO, and Six Sigma requirements.
• Maintain quality assurance procedures, protocols, and methods for materials into finished products.
• Investigate, verify, and disposition nonconforming materials with cross‑functional teams.

Skills

Quality systems

Attention to detail

Documentation practices

Decision making

Independent work

Cross-functional collaboration

Education

Level 6 in Quality or related discipline

Job description

Dexcom Ireland is hiring a Quality Technician to support Quality Control and Quality Assurance in a GMP‑regulated medical device manufacturing environment. You will assist with nonconformance events, audits, and QA/QC documentation while collaborating with cross‑functional teams to ensure product quality and regulatory compliance.

The role emphasizes on‑floor presence, adherence to ISO 13485 and FDA/ISO standards, and ongoing process improvements across the site.