QA Inspector 2 ( RDC ) - 1A Sun- Tues, every other Wednesday, Can work anytime from 5am-5pm

Dexcom • Mesa, AZ

6d • $20 - $31 • Onsite

About The Position

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.
Meet the Team
At Dexcom, we are driven by a shared mission to improve the lives of people living with diabetes through innovative Continuous Glucose Monitoring (CGM) technology. As part of the Quality team, you will play a critical role in ensuring our products meet the highest standards of quality, safety, and compliance before they reach our customers. This is an excellent opportunity to work in a collaborative, fast-paced environment where attention to detail, continuous learning, and a commitment to excellence directly impact patient outcomes.

Requirements

• Strong attention to detail and a commitment to accuracy in documentation, inspections, and quality processes.
• Able to effectively manage multiple priorities while maintaining compliance and meeting deadlines.
• Strong organizational, communication, and problem-solving skills.
• Work well both independently and collaboratively with cross-functional teams.
• Adaptable and willing to learn new processes, systems, and responsibilities.
• Experience working within a regulated environment such as medical device, manufacturing, pharmaceutical, or a related industry.
• Quality-focused mindset and a commitment to continuous improvement.
• Proficiency with Microsoft Office applications and electronic quality systems.
• Understand the importance of Good Documentation Practices (GDP), compliance, and maintaining high-quality standards in a regulated environment.
• Typically requires a minimum of 2-4 years of related experience and a High School diploma/certificate or equivalent.

Nice To Haves

• Experience with Agile/PLM, Oracle, Camstar, or similar systems is preferred.

Responsibilities

• Perform in-process and final document reviews to ensure accuracy, completeness, proper formatting, signatures, dates, and compliance with Good Documentation Practices (GDP).
• Maintain compliance with operating procedures and complete all required training before performing assigned tasks.
• Ensure documentation is legible, complete, and accurate.
• Inspect labels and packaging to verify compliance with established quality standards.
• Review and approve manufacturing line clearance activities to support product quality and compliance.
• Conduct in-process quality audits within manufacturing to ensure adherence to manufacturing documentation and GDP requirements.
• Assist with the Nonconforming Material Report (NCMR) process for commercial and clinical products.
• Perform in-process product inspections and testing activities for commercial and clinical products.
• Develop an understanding of manufacturing processes and quality requirements to effectively support production operations.
• Provide training and guidance to new employees on quality processes and procedures.
• Proactively take on new challenges and support additional responsibilities within the Quality department as business needs evolve.
• Maintain strong organizational practices while managing multiple priorities in a fast-paced environment.
• Perform other duties and projects as assigned.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED