Supplier Quality Engineer II

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:

The incumbent is responsible for performing the duties of a Supplier Quality Engineer 2, as stated in this job description. Performs tasks with moderate oversight from the manager and/or designated senior level Supplier Quality Engineers.

Will assist Senior Quality Engineers in the performance of their duties and will support, evaluate, revise and implement specific aspects of the quality system, as assigned. The incumbent will be systematic, highly organized and articulate, and work well in a team environment. Also to be proficient computer skills in the use of Microsoft Office and database applications (such as Oracle and Agile).

Job tasks require interfacing with external suppliers, internal manufacturing, engineering, regulatory, quality, materials, operations personnel and senior management. Will provide guidance and training to technical and administrative personnel, incoming new hires, as assigned.

A positive attitude is important while working in a fast-paced manufacturing environment and dealing with shifting priorities.

Where you come in:

• You will maintain the supplier quality management system in accordance with established policies and procedures, supporting compliance and continuous improvement initiatives.
• You will provide quality guidance and support to cross‑functional departments as required.
• You will participate in Supplier Review Committee (SRC) meetings, ensuring transparency and effective cross‑functional communication.
• You will conduct global supplier qualification audits, monitor supplier performance, manage corrective actions, and deliver metrics and periodic reports.
• You will maintain and oversee the Supplier Audit Schedule to ensure ongoing compliance.
• You will act as the supplier quality representative during internal audits and for designated supplier engagements.
• You will ensure Quality Agreements are established and maintained; conduct joint business reviews and approve supplier documentation per agreement requirements.
• You will contribute as a member of design teams by supporting design inputs, component and process design, and verification of design outputs against inputs.

What makes you successful:

• You will required a Bachelor’s degree in a technical discipline with 2–5 years relevant experience, or a Master’s degree with 0–2 years equivalent experience.
• You need experience or working knowledge of manufacturing processes including stamping, grinding, electro‑polishing, moulding, and plastics commodities.
• You should have a Strong knowledge of quality and process improvement methodologies such as Six Sigma, Lean Manufacturing, sampling plans, and statistics.
• You can demonstrate initiative to develop and improve systems and processes that enhance product safety, consistency, efficiency, and cost reduction.
• You have the ability to read, write, and interpret specifications, inspection criteria, schematics, and mechanical drawings, and contribute to revisions as needed.
• You have a solid understanding of Design and Process FMEA (DFMEA / PFMEA).
• You have a working knowledge of Quality System Regulations (21 CFR Part 820) and international medical device standards (ISO 9001 / ISO 13485); audit training or certification is desirable.
• You have the ability to work effectively with minimal supervision, communicate professionally in team environments, and provide training and guidance to junior engineers and new hires.

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:

• 15-25% - Ability to travel to the U.S. and internationally.

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.

#DexcomIreland