Quality Technician 3 Back End Nights

We 𝐡𝐚𝐯𝐞 𝐞𝐱𝐜𝐢𝐭𝐢𝐧𝐠 𝐨𝐩𝐩𝐨𝐫𝐭𝐮𝐧𝐢𝐭𝐢𝐞𝐬 𝐟𝐨𝐫 𝐐𝐮𝐚𝐥𝐢𝐭𝐲 𝐓𝐞𝐜𝐡𝐧𝐢𝐜𝐢𝐚𝐧 3'𝐬 𝐨𝐧 𝐁𝐚𝐜𝐤 𝐄𝐧𝐝 𝐍𝐢𝐠𝐡𝐭 𝐒𝐡𝐢𝐟𝐭 🔔

🌙 𝐀 𝐬𝐡𝐢𝐟𝐭 𝐛𝐮𝐢𝐥𝐭 𝐚𝐫𝐨𝐮𝐧𝐝 𝐲𝐨𝐮𝐫 𝐥𝐢𝐟𝐞 \- 𝐰𝐡𝐚𝐭'𝐬 𝐢𝐧 𝐢𝐭 𝐟𝐨𝐫 𝐲𝐨𝐮?

➡️ 𝐘𝐨𝐮 𝐜𝐚𝐧 𝐩𝐥𝐚𝐧 𝐲𝐨𝐮𝐫 𝐥𝐢𝐟𝐞, 𝐧𝐨𝐭 𝐣𝐮𝐬𝐭 𝐲𝐨𝐮𝐫 𝐫𝐨𝐬𝐭𝐞𝐫 \- These roles are on a permanent non-rotational night shift (Friday to Sunday, and alternate Thursdays 7pm to 7am).

🗓️ 𝐖𝐨𝐫𝐤 𝐥𝐞𝐬𝐬 𝐭𝐡𝐚𝐧 𝐡𝐚𝐥𝐟 𝐭𝐡𝐞 𝐲𝐞𝐚𝐫 \- Imagine working only 14 days in every 28!

☕𝐏𝐚𝐢𝐝 𝐛𝐫𝐞𝐚𝐤𝐬 𝐛𝐮𝐢𝐥𝐭 𝐢𝐧 \- Because we know 12-hour shifts should come with proper downtime.

👨‍👩‍👧𝐑𝐞𝐚𝐥 𝐰𝐨𝐫𝐤-𝐥𝐢𝐟𝐞 𝐛𝐚𝐥𝐚𝐧𝐜𝐞 -For many of our team, nights actually enable life: Quality daytime with family and friends, Flexibility for school runs and family routines and the freedom to manage appointments, fitness, and wellbeing while others work

📚𝐓𝐢𝐦𝐞 𝐭𝐨 𝐩𝐮𝐫𝐬𝐮𝐞 𝐟𝐮𝐫𝐭𝐡𝐞𝐫 𝐞𝐝𝐮𝐜𝐚𝐭𝐢𝐨𝐧

This shift has enabled many of our employees to pursue further education they wouldn’t have access to if working a daytime or rotational shift pattern

🕰️Night shift isn’t just different...for the right person, it’s better! It’s engaging, life-enabling and purposeful. Most importantly, it gives you more time for what matters to you, outside of work.

💡 𝐖𝐡𝐚𝐭 𝐦𝐚𝐤𝐞𝐬 𝐭𝐡𝐢𝐬 𝐫𝐨𝐥𝐞 𝐞𝐱𝐜𝐢𝐭𝐢𝐧𝐠?

✔️ Take ownership as a Subject Matter Expert in your area

✔️ With 4–6 years’ experience working in a fast paced manufacturing environment, you won’t just support quality at Dexcom, you’ll help define it.

✔️ You’ll play a key role in decision-making on the manufacturing floor, driving compliance, continuous improvement, and process excellence.

Meet the team:

The Quality Technician at Dexcom Ireland provides hands‑on quality support within a regulated medical device manufacturing environment, ensuring compliance with internal procedures, GMP, and applicable regulatory standards. The role supports day‑to‑day manufacturing operations through execution of routine quality activities, monitoring of in‑process and environmental controls, and assistance with quality documentation and investigations. Working closely with Manufacturing, Engineering, and Quality teams, the Quality Technician contributes to maintaining high standards of product quality, compliance, and continuous improvement across the site.

Where you come in:

You will support Quality Control and Quality Assurance operations, playing a key role in ensuring the quality, compliance, and integrity of manufacturing processes. This role involves processing and analysing nonconformance events, supporting internal and external audits, reviewing and managing quality documentation, and working collaboratively with cross‑functional teams to ensure ongoing product quality. You may also contribute to the development and continuous improvement of quality assurance and quality control methods and procedures.

Essential Duties and Responsibilities (performance expectations vary by level):

• You will support Quality Engineering activities, including Change Order processing, Nonconformance Events (NCEs), Nonconforming Material Reports (NCMRs), and CAPA investigations.
• You will collect manufacturing and inspection data and perform inspections to support investigations led by Quality Engineers.
• You will support production through regular presence on the manufacturing floor and assist the inspection team with questions related to inspection methods, processes, and specifications.
• You will support Quality Engineering in ensuring compliance with internal procedures and external standards and regulations, including GMP, GLP, ISO, and Six Sigma requirements.
• You will update and maintain quality assurance procedures, protocols, and methods for processing materials into partially finished and finished products.
• You must ensure manufacturing and production processes comply with internal quality systems and applicable safety, quality, and regulatory requirements to enable worldwide product distribution.
• You will support the investigation, assessment, verification, and disposition of nonconforming materials in collaboration with cross‑functional teams.
• You will perform routine line audits to verify that systems are compliant, effective, and operating as intended.
• You will provide day‑to‑day quality support to Quality Engineering and Operations by addressing production quality issues and supporting the implementation of corrective and corrective actions.
• You must identify opportunities for quality and process improvement and contribute to continuous improvement initiatives that enhance product quality and process efficiency.
• You must communicate any concerns related to work processes, environmental impact, health, or safety to your manager in a timely manner.
• You must read and interpret specifications, inspection criteria, and engineering drawings, applying requirements using appropriate and properly configured inspection tools.
• You will demonstrate sound decision‑making skills and the ability to work independently with minimal supervision.
• You may assist in the training and mentoring of junior technicians, as required.
• You must apply intermediate computer skills, including effective use of Microsoft Office applications.
• You must demonstrate excellent attention to detail and strong documentation practices. You will perform additional duties as assigned in support of Quality and Operations objectives.

What makes you successful: role specific?

• You will demonstrate 2–4 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 Continuous Glucose Monitoring (CGM) technology, with the opportunity to make a meaningful impact for our global #DexcomWarriors community.
• A competitive and comprehensive benefits package designed to support your health, wellbeing, and financial security.
• Career growth opportunities on a global scale, within a rapidly growing and innovative organization.
• Access to ongoing career development, including in‑house learning programs and qualified tuition reimbursement.
• The opportunity to work with an exciting, industry‑leading organisation that is committed to its employees, customers, and the communities it serves.

Experience and Education Requirements:

• Level 6 in Quality or a related discipline.
• Minimum of 2 years of experience in a regulated industry.
• Knowledge of ISO 13485, 21 CFR Part 11, 21 CFR 820,
• Experience working on cross site or global system projects. Audit experience with FDA, BSI, or MDSAP. Experience with manufacturing systems, MES, ERP, or QMS applications.