Additional Information
The Company
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 an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.
We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.
Reports to: Production Supervisor
Start Date: August 2026
Shift Details: 12-hour shifts | 4-on / 3-off - 3-on / 4-off pattern
Friday to Sunday + alternate Thursdays
As a Manufacturing Associate 2 (MA2), you play a critical role in producing Dexcom's life‑changing Continuous Glucose Monitoring (CGM) products. Operating within a cleanroom environment, you will work with semi‑automated and fully automated equipment to ensure our products meet the highest standards of quality, safety, and compliance.
This role suits individuals with medical device or regulated manufacturing experience, excellent attention to detail, and comfort working in a fast‑paced, high‑volume production environment.
Where you come in (essential duties & responsibilities):
Operate and monitor semi‑automated and automated equipment.
Carry out routine manual tasks such as handling components, loading materials, and supporting assembly processes as required.
Perform precise, dexterity‑based assembly tasks and maintain consistent output.
Perform in‑process checks to ensure product quality.
Complete packaging, labelling, material movement, and required data entry.
Follow all GMP, SOPs, batch records, and cleanroom protocols, completing documentation accurately.
Report any deviations, defects, or safety concerns immediately and support quality and yield targets.
Work closely with supervisors and team members, ensuring clear communication and smooth shift handovers.
Support a culture of safety, quality, and continuous improvement.
Achieve competency within training timelines and consistently meet output and quality KPIs.
Demonstrate reliability, accuracy, and adherence to standardised processes.
What makes you successful:
Leaving Certificate (or Level 5 equivalent).
2+ years in medical device or regulated manufacturing.
Strong attention to detail and ability to follow structured procedures.
Comfort with repetitive, hands‑on assembly tasks.
Good computer literacy and mechanical aptitude.
Reliable, adaptable, and team oriented.
Excellent communication skills
Dexcom · Athenry, Ireland