QA Engineer 2

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. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered the industry, and we are just getting started. We are broadening our vision beyond diabetes to empower people to take control of health with personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.

Our Quality Assurance team is looking for the right teammate to support the start‑up of our first European manufacturing site in Athenry. As a QA Engineer, you will play an integral part in the validation and quality assurance of site equipment, utilities and processes in compliance with Dexcom procedures. This crucial role supports Dexcom’s thrilling growth trajectory in delivering essential, life‑changing products to our valued customers. As part of this dynamic and highly effective team, you will collaborate closely across multiple functions, gaining broad exposure to our entire product life cycle.

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• You will coordinate and actively participate in the validation and quality assurance of site equipment, utilities and processes in compliance with Dexcom procedures, including equipment with a high degree of automation.
  
• You will review validation protocols and final reports, ensuring they meet cGMP standards.
  
• You will manage validation investigations and implement corrective actions as needed.
  
• You will communicate regularly with peers and management regarding activities, escalating issues or concerns as necessary.
  
• You will design methods and procedures for inspecting, testing and evaluating the precision and accuracy of production processes, production equipment and finished products.
  
• You will apply concepts, principles and techniques of statistics to datasets, identifying patterns and drawing actionable insights.
  
• You will participate in continuous improvement programs to enhance manufacturing, quality, safety and training systems.
  
• You will review, update and maintain existing quality management processes and procedures.
  
• You will initiate non‑conformances/CAPAs and complete investigations as required.
  
• You will perform risk management activities (e.g., FMEA, risk assessments) to ensure the safety and effectiveness of products.
  
• You will be responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards for worldwide distribution.
  
• You will monitor and report on quality metrics, such as defect rates and process capability.
  
• Assume and perform other duties as assigned.
  

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• You will have QA experience in process and equipment validation, with hands‑on experience in end‑to‑end process validation.
  
• Experience in automation validation is highly desirable.
  
• You will be proficient in Microsoft Office and database applications (e.g., Excel and MiniTab or similar).
  
• You will have critical thinking, solid decision‑making and problem‑solving skills.
  
• You will have strong written and oral communication and presentation skills.
  

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• A front‑row seat to life‑changing CGM technology. Learn about our brave #dexcomwarriors community.
  
• A full and comprehensive benefits program.
  
• Growth opportunities on a global scale.
  
• Access to career development through in‑house learning programs and/or qualified tuition reimbursement.
  
• An exciting and innovative, industry‑leading organization committed to our employees, customers and the communities we serve. xcfaprz
  

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• 5‑15%
  

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• Typically requires a Bachelor’s degree in a technical discipline and a minimum of 2‑5 years related experience, or a Master’s degree and 0‑2 years’ equivalent experience.