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

Dexcom Inc.; Mesa (AZ); On-site; USD 28,000 - 41,000; Full time

Job summary

Dexcom Inc. is seeking a Quality team member in Mesa, AZ to ensure documentation and manufacturing quality meet GDP standards. You will review in-process and final documents, inspect labels/packaging, and support line clearance activities.

Ideal candidates have 2–4 years of related experience in regulated environments and strong organizational and problem-solving skills. The role emphasizes accuracy, cross-functional collaboration, and continuous improvement within a fast-paced setting.

Qualifications

• 2–4 years of related experience and a High School diploma/certificate or equivalent.
• Experience in a regulated environment such as medical device or manufacturing is preferred.
• Familiarity with GDP and quality documentation practices is expected.

Responsibilities

• Perform in-process and final document reviews for GDP compliance.
• Inspect labels and packaging against established quality standards.
• Review and approve manufacturing line clearance activities.
• Conduct in-process quality audits within manufacturing.
• Assist with the Nonconforming Material Report (NCMR) process.
• Perform in-process product inspections and testing for products.

Skills

Attention to detail

Documentation

Communication

Problem-solving

Organizational skills

Cross-functional collaboration

Agile/PLM experience

Education

High School diploma or equivalent

Tools

Microsoft Office

Oracle

Camstar

PLM systems

Job description

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.

Where You Come In:

• 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.

What Makes You Successful:

• 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.

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.

Travel Required:

• 0-5%

Experience and Education Requirements:

• 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 of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at [e-mail].

If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at [e-mail].

Salary: $20.48 - $30.67