More jobs:
Director, Quality Audits San Diego, California + 1 more Posted a day ago
Job in
San Diego, San Diego County, California, 92189, USA
Listed on 2026-08-07
Listing for:
Dexcom Inc.
Full Time
position Listed on 2026-08-07
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Job Description & How to Apply Below
120298
** 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:
** The Quality Compliance team at Dexcom plays a critical role in ensuring the integrity, effectiveness, and scalability of our global Quality Management System (QMS). As a key function within Global Quality, we are responsible for ensuring our products remain safe, effective, and compliant with global regulatory requirements while supporting Dexcom's mission to empower people to take control of health through innovative glucose biosensing technology.
We partner across the organization to enable innovation, drive operational excellence, and maintain the highest standards of quality and compliance. As Dexcom continues to expand globally, the Quality Compliance team leads the evolution of our quality systems and processes to meet increasingly complex regulatory requirements while ensuring agility, efficiency, and scalability.
** Where you come in:
** You will:
* Provide strategic leadership for Dexcom's global Quality Audit program, ensuring a risk-based approach that drives compliance, operational excellence, and continuous improvement.
* Establish and lead a Corporate Audit program that proactively identifies, assesses, and mitigates quality and compliance risks across the enterprise.
* Drive global standardization and effectiveness of the Internal Audit program while partnering closely with sites and functional teams to ensure consistent execution.
* Ensure ongoing inspection readiness across the organization by strengthening audit capabilities, monitoring compliance trends, and partnering with key stakeholders.
* Build, develop, and lead a high-performing global audit organization, fostering a culture of accountability, collaboration, and continuous development.
* Leverage audit insights, metrics, and leading indicators to identify systemic risks, drive proactive improvements, and enhance the effectiveness of the Quality Management System.
* Serve as a trusted partner to cross-functional leaders, influencing strategic decisions and driving sustainable solutions to complex compliance and quality challenges.
* Champion a culture of quality, compliance, and continuous improvement throughout the organization.
* Provide executive leadership with clear, data-driven reporting on audit performance, emerging risks, inspection readiness, and strategic improvement opportunities.
** What makes you successful:
*** You are a strategic Quality Compliance leader who combines deep regulatory expertise with strong business acumen, enabling you to assess complex risks, influence stakeholders, and drive meaningful organizational changes.
* Deep knowledge of global medical device quality and regulatory requirements, including FDA QMSR, ISO 13485, EU MDR, MDSAP, and other applicable international regulations and standards.
* Proven track record leading audit programs with successful outcomes and sustained compliance results.
* Extensive experience designing, implementing, and continuously improving risk-based audit programs in a global regulated environment.
* Demonstrated expertise as a Lead Auditor, with the ability to evaluate complex quality systems and identify opportunities for systemic improvement.
* Strong analytical mindset with the ability to leverage data, trends, and leading indicators to drive proactive risk management and quality system enhancements.
* Ability to anticipate evolving regulatory expectations and translate them into scalable, business-focused compliance strategies.
* Exceptional communication and influencing skills, with the ability to effectively engage and align stakeholders from frontline teams to executive leadership.
*…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×