Quality Engineer II – Medical Devices Impact

1 DexCom Inc

Colorado

On-site

USD 72,000 - 119,000

Full time

4 days ago
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Benefits offered by this job

Comprehensive benefits program
Career development opportunities
Global growth opportunities

Job summary

Dexcom is seeking a Quality Engineer II to join our Quality organization, driving quality across the product lifecycle for life-changing CGM technology. You will lead investigations, strengthen quality systems, influence product and process design, and enable data‑driven decisions while mentoring engineers and elevating risk‑based thinking.

You will collaborate with cross‑functional teams in Operations, R&D, Regulatory, and Manufacturing to deliver safe, effective medical devices that meet

Qualifications

  • Bachelor’s degree in a technical discipline with 2–5 years of related experience, or a Master’s degree with 0–2 years of equivalent industry experience.
  • Proficiency with statistical tools, root cause analysis, validation, and risk-based problem solving.
  • Strong communication skills for both technical and non-technical audiences.
  • Ability to thrive in a fast-paced environment and manage multiple priorities.

Responsibilities

  • Implement and maintain quality assurance protocols for processing materials into finished or semi-finished products.
  • Ensure compliance to in-house and external specifications and standards (GLP, GMP, ISO, Six Sigma).
  • Complete investigations into nonconformances.
  • Assist in high-visibility quality engineering projects with cross-functional teams.
  • Identify systemic issues and drive long-term corrective and preventive actions.

Job description

Dexcom is seeking a Quality Engineer II to join our Quality organization, driving quality across the product lifecycle for life-changing CGM technology. You will lead investigations, strengthen quality systems, influence product and process design, and enable data‑driven decisions while mentoring engineers and elevating risk‑based thinking.

You will collaborate with cross‑functional teams in Operations, R&D, Regulatory, and Manufacturing to deliver safe, effective medical devices that meet

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