QA Inspector 1 ( 2A – Sunday to Tuesday, every other Wednesday; can work anytime from 5 PM to 5 AM)

Dexcom • Mesa, AZ

11h • $19 - $28

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: Founded in 1999, Dexcom, Inc. (NASDAQ: DXCM), develops and markets Continuous Glucose Monitoring (CGM) systems for ambulatory use by people with diabetes and by healthcare providers for the treatment of people with diabetes. The company is the leader in transforming diabetes care and management by providing CGM technology to help patients and healthcare professionals better manage diabetes.Since the company's inception, Dexcom has focused on better outcomes for patients, caregivers, and clinicians by delivering solutions that are best in class - while empowering the community to take control of diabetes. Where You Come In: You perform in‑process and final product reviews of documents to ensure accurate format, signatures, dating, and full adherence to Good Documentation Practices (GDP) for commercial and clinical products. You maintain compliance with operating procedures and ensure all training is completed before performing any task. You ensure all documentation is legible, complete, and correct. You inspect labeling for finished products. You understand, review, and approve line clearance activities in manufacturing. You perform in‑process quality audits in manufacturing to verify compliance with documentation and GDP. You assist with the NCMR process during manufacturing for commercial and clinical products. You perform in‑process product inspections and testing for commercial and clinical products. You familiarize yourself with manufacturing processes. You provide training to new employees. You take on new challenges and expanded responsibilities to support growing demands within different areas of the Quality Department. You have strong organizational skills and attention to detail. You assume and perform other duties as assigned. What Makes You Successful: You are able to perform all essential duties of the role efficiently and accurately. You have strong organizational skills, attention to detail, and a commitment to quality. You bring proficiency in reviewing documentation, applying GDP, and supporting manufacturing processes. You ideally have experience with Agile/PLM, Oracle, and/or Camstar software programs. (Nice to have) You demonstrate adaptability, willingness to learn, and the ability to support multiple quality functions as needed. Your communication skills and accuracy make you a key partner in ensuring compliance and product integrity. What you'll get: 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.

Requirements

• You are able to perform all essential duties of the role efficiently and accurately.
• You have strong organizational skills, attention to detail, and a commitment to quality.
• You bring proficiency in reviewing documentation, applying GDP, and supporting manufacturing processes.
• You demonstrate adaptability, willingness to learn, and the ability to support multiple quality functions as needed.
• Your communication skills and accuracy make you a key partner in ensuring compliance and product integrity.
• Typically requires 0- 2 years of related experience and a High school diploma/certificate or equivalent.

Nice To Haves

• You ideally have experience with Agile/PLM, Oracle, and/or Camstar software programs.

Responsibilities

• You perform in‑process and final product reviews of documents to ensure accurate format, signatures, dating, and full adherence to Good Documentation Practices (GDP) for commercial and clinical products.
• You maintain compliance with operating procedures and ensure all training is completed before performing any task.
• You ensure all documentation is legible, complete, and correct.
• You inspect labeling for finished products.
• You understand, review, and approve line clearance activities in manufacturing.
• You perform in‑process quality audits in manufacturing to verify compliance with documentation and GDP.
• You assist with the NCMR process during manufacturing for commercial and clinical products.
• You perform in‑process product inspections and testing for commercial and clinical products.
• You familiarize yourself with manufacturing processes.
• You provide training to new employees.
• You take on new challenges and expanded responsibilities to support growing demands within different areas of the Quality Department.
• You have strong organizational skills and attention to detail.
• You assume and 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: Entry Level
• Education Level: High school or GED