Company Overview
Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Founded 25 years ago with the mission to transform diabetes management, Dexcom now aims to broaden its vision to empower individuals to take control of their health through personalized, actionable insights. Our goal is to continue improving human health on a global scale.
Driven by passionate and ambitious individuals worldwide, we strive to earn customer trust through integrity, innovation, and dependability. Our future ambitions include becoming a leading consumer health technology company, developing innovative biosensing technologies, and expanding our impact in serious health conditions.
Meet The Team
The role involves performing duties as a Supplier Quality Engineer II, with moderate oversight. You will assist senior engineers, support quality system improvements, and work collaboratively with external suppliers and internal teams. Proficiency in Microsoft Office and database applications like Oracle and Agile is required. Effective communication and a positive attitude are essential in our fast-paced environment.
Responsibilities
* Maintain the supplier quality management system and contribute to process improvements.
* Provide quality guidance across departments.
* Participate in Supplier Review Committee meetings, ensuring transparency and communication.
* Conduct global supplier audits, monitor performance, and manage corrective actions.
* Maintain the Supplier Audit Schedule and ensure compliance.
* Represent quality during internal audits and for designated suppliers.
* Establish Quality Agreements and review supplier documentation.
* Assist in design activities, including defining inputs and verifying outputs.
Qualifications
* Bachelor’s degree in a technical discipline with 2-5 years of experience, or a Master’s degree with 0-2 years of experience.
* Experience in stamping, grinding, electro-polishing, molding, plastics.
* Knowledge of Six Sigma, lean manufacturing, sampling plans, and statistics.
* Ability to develop systems that improve safety, consistency, efficiency, and reduce costs.
* Understanding of specifications, schematics, and mechanical drawings.
* Knowledge of FMEA methodologies and medical device quality standards (ISO 9001, ISO 13485, 21 CFR Part 820).
* Previous training or certification in quality audits is preferred.
* Support training of junior staff and work effectively in a team.
Benefits
* Access to life-changing CGM technology and community.
* Comprehensive benefits and global growth opportunities.
* In-house learning and tuition reimbursement programs.
* Work in an innovative organization committed to its employees and communities.
Travel Requirements
15-25% travel, domestically and internationally.
Note: Our careers site is exclusively for individuals seeking employment at Dexcom. Unsolicited resumes from staffing agencies will not be accepted, and Dexcom is not responsible for fees related to such resumes.
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