Supplier Quality Engineer 2

The incumbent is responsible for performing the duties of a Supplier Quality Engineer 2, with tasks performed 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. Proficient computer skills in the use of Microsoft Office and database applications (such as Oracle and Agile).

• 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.

• You will require 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.

• 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.

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

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