QA Engineer, Digital Systems — Growth & Impact in MedTech

Dexcom Ireland - Athenry; Athenry; On-site; EUR 55,000 - 75,000; Full time

Job summary

Dexcom Ireland is seeking a QA Engineer to ensure quality across site processes and digital manufacturing, contributing to our CGM technology leadership. You will validate manufacturing and digital systems, develop standardized validation templates, and apply risk-based validation to system implementations and changes.

The role supports CAPAs, NCMRs, and regulatory readiness within a growing team. Ideal candidates have a technical degree with 2–5 years in medical device quality, experience with

Qualifications

• Typically requires a Bachelor's degree in a technical discipline with 2–5 years of related experience.
• Experience in Quality in a medical device or related industry manufacturing environment.
• Experience with CAPA, NCMAs and problem-solving tools.
• Experience in digital systems and continuous improvement initiatives preferred.

Responsibilities

• Validate manufacturing and digital systems exposure.
• Develop and apply standardized validation templates and practices.
• Apply risk-based validation for digital manufacturing systems.
• Plan, manage and prioritize validation tasks; provide progress updates to management.
• Address OOS events, CAPAs, NCMRs and Change Orders; communicate with stakeholders.
• Support integration of new regulations or QMS standards; drive documentation revisions.
• Support ongoing improvement and maintenance of the QMS and audit readiness.

Skills

CAPA

Non-Conformance

Problem-solving

Digital systems

Continuous improvement

Microsoft Office

Excel

MiniTab

Database applications

Education

Bachelor’s degree in a technical discipline

Master’s degree (optional)

Tools

MiniTab

Database software

Job description

Dexcom Ireland is seeking a QA Engineer to ensure quality across site processes and digital manufacturing, contributing to our CGM technology leadership. You will validate manufacturing and digital systems, develop standardized validation templates, and apply risk-based validation to system implementations and changes.

The role supports CAPAs, NCMRs, and regulatory readiness within a growing team. Ideal candidates have a technical degree with 2–5 years in medical device quality, experience with