QA Inspector 3

DexCom • Mesa, AZ

4d • $24 - $36

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: Dexcom transforms diabetes care through world‑class Continuous Glucose Monitoring (CGM) technology. Our Lot Release organization ensures only fully compliant, safe, and high‑quality product is released to the global market. As part of this team in Mesa, AZ, you’ll support Lot Release processes for Dexcom’s G6/G7 sensors, solutions, and finished goods by applying strong documentation review, Good Documentation Practices (GDP), and a continuous improvement mindset. Where you come in: You will serve as a cross‑shift continuity resource, providing consistent Quality support across multiple days of the week and acting as a flexible, reliable resource during workload peaks. You will support internal and external audits, continuous improvement initiatives, and cross‑functional activities. You will competently perform and support QA LHR review and release processes across all applicable operations. You will perform in‑process and final product review of documents for accurate format, signatures, dating, and Good Documentation Practices (GDP) for commercial and clinical products in a timely manner. You will maintain compliance with operating procedures and ensure all required training is completed prior to performing any task. You will inspect labeling for finished products. You will assist with the NCMR process for commercial and clinical products. You will perform in‑process product inspection/testing/AQL for commercial and clinical products. You will develop a working understanding of manufacturing processes to support quality oversight. You will provide training and guidance to new employees. You will take on new challenges and responsibilities to support evolving needs within the Quality Department. You will demonstrate strong organizational skills and attention to detail. You will perform other duties as assigned.

Requirements

• Requirements listed above represent the knowledge, skills, and abilities essential for successful performance. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
• Typically requires a minimum of 4-6 years of related experience and High School diploma/certificate or equivalent.

Nice To Haves

• Experience with Agile/PLM, Oracle, Camstar systems, and other associated systems.
• Demonstrated proficiency in reviewing and approving Dexcom LHRs at the QA step for all processes supported at the Dobson Manufacturing Site.
• Ability to perform all essential duties independently, accurately, and with a strong sense of ownership.

Responsibilities

• Serve as a cross‑shift continuity resource, providing consistent Quality support across multiple days of the week and acting as a flexible, reliable resource during workload peaks.
• Support internal and external audits, continuous improvement initiatives, and cross‑functional activities.
• Competently perform and support QA LHR review and release processes across all applicable operations.
• Perform in‑process and final product review of documents for accurate format, signatures, dating, and Good Documentation Practices (GDP) for commercial and clinical products in a timely manner.
• Maintain compliance with operating procedures and ensure all required training is completed prior to performing any task.
• Inspect labeling for finished products.
• Assist with the NCMR process for commercial and clinical products.
• Perform in‑process product inspection/testing/AQL for commercial and clinical products.
• Develop a working understanding of manufacturing processes to support quality oversight.
• Provide training and guidance to new employees.
• Take on new challenges and responsibilities to support evolving needs within the Quality Department.
• Demonstrate strong organizational skills and attention to detail.
• Perform other duties 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