QA Inspector ( Dobson ) Shift: Sun-Tues, Sat

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.

Join Dexcom's Quality team and play a critical role in ensuring the integrity, safety, and quality of life-changing Continuous Glucose Monitoring (CGM) products. As a Quality Inspector, you will work closely with cross-functional teams to support manufacturing operations, maintain compliance standards, and help ensure that every product meets the highest quality expectations. If you are passionate about accuracy, continuous improvement, and making a meaningful impact on the lives of people with diabetes, this is an exciting opportunity to grow your career with an industry leader.

• You will perform in-process and final product reviews of documentation to ensure accuracy, completeness, proper formatting, signatures, dates, and compliance with Good Documentation Practices (GDP).
• You will maintain compliance with operating procedures and complete all required training before performing assigned tasks.
• You will ensure manufacturing documentation is legible, complete, accurate, and compliant with quality requirements.
• You will inspect finished product labeling to verify compliance with specifications and regulatory requirements.
• You will review and approve line clearance activities to support manufacturing readiness.
  
  You will perform in-process quality audits within manufacturing areas to ensure compliance with manufacturing procedures and GDP standards.
• You will assist with Non-Conforming Material Report (NCMR) activities during the manufacturing of commercial and clinical products.
• You will conduct in-process product inspections and testing to verify quality requirements are met.
• You will develop a strong understanding of manufacturing processes to effectively support quality operations.
• You will provide training and guidance to new team members as needed.
• You will embrace new challenges and support evolving business needs across various areas within the Quality Department.
• You will maintain strong organizational skills and attention to detail while managing multiple priorities.
• You will perform additional duties and responsibilities as assigned.

• You are detail-oriented and committed to maintaining high standards of quality and compliance.
• You have the ability to review documentation accurately and identify inconsistencies or errors.
• You are highly organized and can effectively manage competing priorities in a fast-paced environment.
• You have strong communication and collaboration skills and work well within cross-functional teams.
• You bring a proactive mindset and a willingness to learn new processes, systems, and responsibilities.
• You have experience working in a regulated manufacturing, quality, or medical device environment, preferred.
• You have familiarity with Good Documentation Practices (GDP), quality systems, and manufacturing processes.
• You have experience using or can quickly learn systems such as Agile/PLM, Oracle, Camstar, or similar software platforms.
• You are committed to continuous improvement and delivering high-quality results that support patient safety and product excellence.

• A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
• A full and…