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Regulatory Affairs Specialist San Diego, California Posted 19 hours ago
Job in
San Diego, San Diego County, California, 92189, USA
Listed on 2026-08-05
Listing for:
Dexcom Inc.
Part Time
position Listed on 2026-08-05
Job specializations:
-
Science
Data Scientist, Healthcare Compliance
Job Description & How to Apply Below
Join Talent Network# Single Position View All Jobs Hybrid## Regulatory Affairs Specialist San Diego, California Find out how well you match with this jobJob IDJR
120047
** 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:
** Regulatory Affairs is a team of more than 40 professionals located either at San Diego HQ or remotely around the globe. Our backgrounds range from biological and physical sciences to engineering, political science to biostatistics, pharmacology to law just to name a few. Our degrees include Bachelor’s, Master’s, Ph.D.’s, JD’s and more. With our various backgrounds and talents we help to navigate and align the ideas and output of most facets of the company to successfully get our home-use products to our end users.
We’re closely connected with QA, Clinical, IT, and Global Business Solutions (GBS) under the same Executive Vice President. At our quarterly onsite gatherings, some of our pastimes include story sharing, cooking and baking, social events and other team-building activities.
If you join our team you will be supporting the growth and expansion of Dexcom’s Continuous Glucose Monitoring (CGM) Systems.
** Where you come in:
*** You will support developmental activities for Dexcom software products.
* You will develop regulatory strategies and prepare submissions in various countries (US, EU, Canada).
* You will collaborate with regional regulatory teams to develop global strategies as required.
* You will review and approve product and promotional labeling for software.
* You will represent Regulatory Affairs on various cross-functional software teams.
* You will review and approve software documentation and evaluate for submission requirements.
* You will take on additional projects and responsibilities as needed.
** What makes you successful:
*** You bring knowledge of US and international regulatory requirements including design control, medical device submission requirements, labeling and promotion regulations, and medical device quality systems.
* You have Medical Device Software experience and/or knowledge, such as software development lifecycle, IEC 62304, and software classification.
* You have strong technical writing, editing, and analytical skills.
* You work well independently and with cross-functional teams.
* You thrive in a fast-paced environment and adapt quickly to changing priorities.
* You are proficient in problem solving, proactive learning, organization, and have excellent communication skills.
* Having previous experience with 510(k) submissions, Health Canada submissions, or EU Medical Device Regulation is preferred.
** 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…
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