Quality Support 2

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.

Summary

Assist with the day-to-day operations associated with Control of Nonconforming Materials. Assist management to ensure that products, procedures, and processes comply with applicable regulations and standards.

Essential Duties And Responsibilities

• Perform physically quarantine nonconforming material.
• Perform electronic inventory transactions to prevent unintended use.
• Execute activities per approved material disposition.
• Facilitate NCMR processing in the electronic system.
• Monitor NCMR trending, follow-up NCMR status, and reporting.
• Maintain inventory under Quality Control through transactions and cycle counts.
• Assist with the identification and organization of quality records associated with Nonconforming Material with cross department personnel.
• Support investigations into potential quality/compliance concerns.
• Support routine walk-through activities.
• Perform other tasks as assigned to enable organizational and quality objectives to be met.

Required Qualifications

• Minimum 3 years working in the medical device, pharmaceutical, or other regulated industry in the Quality Assurance department.
• Understanding of Quality Management Systems (QMS) as applied to medical devices.
• Proficiency with Microsoft Office, ERP System.
• Ability to communicate effectively and clearly.
• Ability to work hands-on in a fast-paced environment.
• Must be able to flex schedule to work in different shifts to support commercial run.