Remote Senior Software QA Engineer – Medical Devices

Dexcom Inc.; San Diego (CA); On-site; USD 96,000 - 160,000; Full time

Job summary

Dexcom Inc. seeks a Senior Software QA Engineer in San Diego, CA to lead postmarket investigations and ensure software quality across the product lifecycle. This role partners with Regulatory Affairs, QA, R&D, Clinical, and Process Engineering to investigate postmarket issues and drive corrective actions.

Applicants should bring knowledge of FDA/ISO regulations, strong analytics, and excellent communication to translate data into actionable improvements for patient safety and product reliability.

Qualifications

• Bachelor’s degree in a technical discipline required.
• 5–8 years related experience or Master’s with 2–5 years or PhD with 0–2 years experience as stated in job post.
• Experience with software quality engineering across the product lifecycle.

Responsibilities

• Collaborate with Regulatory Affairs, QA, R&D, Clinical and Process Engineering to investigate postmarket issues.
• Drive development and improvement of complaint investigation processes with risk management alignment.
• Analyze product performance, investigate anomalies, and identify root causes using data.
• Communicate investigation outcomes to stakeholders to support decision-making.

Skills

Software quality engineering

Regulatory compliance

Analytical mindset

Communication skills

Data-driven decision making

Problem solving

Education

Bachelor’s degree in technical discipline

Master’s degree

PhD

Tools

Cloud platforms

Distributed systems

Cybersecurity basics

Job description

Dexcom Inc. seeks a Senior Software QA Engineer in San Diego, CA to lead postmarket investigations and ensure software quality across the product lifecycle. This role partners with Regulatory Affairs, QA, R&D, Clinical, and Process Engineering to investigate postmarket issues and drive corrective actions.

Applicants should bring knowledge of FDA/ISO regulations, strong analytics, and excellent communication to translate data into actionable improvements for patient safety and product reliability.