QA Inspector ( Dobson; Sun- Tues

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.

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

• You have strong attention to detail and a commitment to accuracy in documentation, inspections, and quality processes.
• You are able to effectively manage multiple priorities while maintaining compliance and meeting deadlines.
• You have strong organizational, communication, and problem-solving skills.
• You work well both independently and collaboratively with cross-functional teams.
• You are adaptable and willing to learn new processes, systems, and responsibilities.
• You have experience working within a regulated environment such as medical device, manufacturing, pharmaceutical, or a related industry.
• You bring a quality-focused mindset and a commitment to continuous improvement.
• You have proficiency with Microsoft Office applications and electronic quality systems.
• Your experience with Agile/PLM, Oracle, Camstar, or similar systems is preferred.
• You understand the importance of Good Documentation Practices (GDP), compliance, and maintaining high-quality standards in a regulated environment.

• 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.

• 0-5%

• Typically requires a minimum of 2-4 years of related experience and a High School diploma/certificate or equivalent.

The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list…