Process Development Engineer

Position: Process Development Engineer 1
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:

Dexcom is hiring for a Process Development Engineer I to join our dynamic team in San Diego, CA. In this role within the Global Engineering organization, you will support the development and implementation of manufacturing and test processes for continuous glucose monitoring (CGM) devices. You will contribute to process characterization, experimentation, troubleshooting, and continuous improvement efforts while collaborating with cross-functional partners across Engineering, Manufacturing, Quality, and Operations.

Where you come in:

You support the development of process formulations and test methods used in the manufacture and testing of materials and products.

You assist in defining processing, handling, equipment, and test requirements with guidance from engineers and cross-functional partners.

You plan, execute, and document experiments to characterize new processes and test methods.

You compile, trend, and evaluate test data to identify process variables, material contributors, and appropriate limits or specifications.

You collaborate with Manufacturing, Quality, Automation, Software, Analytical Chemistry, and other Engineering teams to gather requirements, troubleshoot issues, and support implementation of new processes.

You prepare technical documentation including protocols, reports, procedures, study summaries, and inputs to risk documentation such as pFMEAs.You participate in design reviews, process reviews, failure investigations, root cause analyses, and continuous improvement activities for new and existing products and processes.

What makes you successful:

You have a foundational understanding of process development, manufacturing processes, test method development, engineering experimentation, and data-driven problem solving.

You demonstrate strong hands-on laboratory, manufacturing, or testing capabilities with attention to detail, safety, and documentation.

You possess the ability to analyze data and draw conclusions to support engineering decisions and process improvements.

You have exposure to Design of Experiments (DOE), statistical analysis, root cause analysis, or data visualization tools such as JMP, Minitab, Python, Excel, or similar platforms.

You can develop clear technical documentation including protocols, reports, procedures, and study summaries.

You demonstrate strong communication and collaboration skills when working with cross-functional stakeholders.

You are able to manage multiple priorities in a fast-paced environment while maintaining high-quality work.

Your curiosity, initiative, and willingness to learn enable you to contribute effectively to engineering projects and continuous improvement efforts.

Your familiarity with FDA-regulated environments, ISO 13485, or medical device manufacturing is preferred but not required.

What you’ll get:

A front row seat to life changing CGM technology.…