Quality Technician II – GMP/QA for Medical Devices

Dexcom Inc.; Ireland; Remote; EUR 37,000 - 48,000; Full time

Benefits offered by this job

CGM technology impact

Benefits package

Global career growth

In‑house learning programs

Tuition reimbursement

Job summary

Dexcom Ireland seeks a Quality Technician to provide hands-on quality support within a regulated medical device manufacturing environment, ensuring compliance with GMP and applicable regulatory standards and contributing to product quality and continuous improvement across the site.

You will support Quality Control and Quality Assurance operations, processing nonconformance events, audits, and quality documentation while collaborating with cross-functional teams; 2–4 years in a regulated setting

Qualifications

• 2–4 years of experience in a medical device or similarly regulated manufacturing environment.
• Knowledge of ISO 13485, 21 CFR Part 11, 21 CFR 820.
• Experience with cross-site or global system projects; audit experience with FDA, BSI, or MDSAP.

Responsibilities

• Support Quality Engineering activities: Change Order processing, Nonconformance Events, CAPA investigations.
• Collect manufacturing and inspection data to support investigations.
• Support production on the manufacturing floor and assist inspection teams.
• Ensure compliance with GMP, GLP, ISO, Six Sigma requirements; update QA procedures.
• Identify opportunities for quality and process improvement.

Skills

Quality awareness

Attention to detail

Analytical thinking

Communication skills

Education

Level 6 in Quality

Tools

MES

ERP

QMS

Job description

Dexcom Ireland seeks a Quality Technician to provide hands-on quality support within a regulated medical device manufacturing environment, ensuring compliance with GMP and applicable regulatory standards and contributing to product quality and continuous improvement across the site.

You will support Quality Control and Quality Assurance operations, processing nonconformance events, audits, and quality documentation while collaborating with cross-functional teams; 2–4 years in a regulated setting