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

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

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.

Please note: 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 View email address on aiapply.co.

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 View email address on aiapply.co.

Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided:

To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

AI in Hiring Notice: We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people.

Salary:

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