Sr Director, QMS

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 Management Systems (QMS) team at Dexcom plays a critical role in ensuring the integrity, compliance, and scalability of our global quality framework. As a strategic function within Global Quality, the teamis responsible formaintaininga robust, compliant, and continuously improving QMS that supports product development, manufacturing, and post-market activities across all regions.

We partner cross-functionally with R&D, Regulatory Affairs, Manufacturing, Supply Chain, and Commercial teams to embed quality into every stage of the product lifecycle. Our mission is to enable innovation whilemaintainingthe highest standards of safety, compliance, and patient impact. As Dexcom continues to grow globally, the QMS team ensures our processes evolve to meet increasingly complex regulatory requirements while staying efficient and scalable.

Where you come in:

As the Sr. Director of Quality Management Systems, you will provide strategic leadership and oversight for Dexcom’s global QMS, ensuring it meets all applicable regulatory requirements (FDA, ISO 13485, MDR, and other international standards) while supporting business growth and innovation.

You will:

• Own and evolve the global QMS strategy, ensuring alignment with corporateobjectivesand regulatory expectations
• Lead the design, implementation, and/orcontinuous improvement of key QMS processes, including document control, CAPA,metrics and analytics,partnershipmanagement,audit management,amongothers.
• Own thecorporateCAPA program,ensuring world class execution andperformance.
• Drive harmonization and standardization of quality processes across global sites and regions
• EstablishaQualityIntelligence program that focuses onrisks and developments across the medical device industry.
• OwnProjectManagementfor the Qualityorganization, focusing on continuous improvement opportunities.
• Ensure inspection readiness at all timesandassistwithenterprise-level responses to regulatory inspections and audits
• Partner closely with Regulatory Affairs to interpret evolving global regulations and proactively integrate requirements into the QMS
• Build, develop, and lead a high-performing,globalQMS team
• Champion a culture of quality, compliance, and continuous improvement across the organization
• Leverage digital tools and data analytics to modernize and scale the QMS, improving efficiency and visibility
• Provide executive-level reporting on QMS performance, risks, and improvement initiatives

What makes you successful:

You are a strategic, forward-thinking quality leader who can balance compliance with agility in a fast-paced,innovation-driven environment.

Leadership & Influence

• Proven ability to lead and scale global teams, driving alignment across functions and geographies
• Strong executive presence with the ability to influence senior leadership and cross-functional stakeholders

Quality & Regulatory Expertise

• Deep knowledge of global QMS requirements, including FDA 21 CFR Part 820, ISO 13485, EU MDR, and other international standards
• Demonstrated success leading regulatory inspections and audits with positive outcomes
• Experience building or transforming QMS frameworks inacomplex, global organization

Operational Excellence

• Track recordof implementing scalable, efficient quality processes that support rapid business growth
• Strong systems mindset with experience driving digital transformation within QMS platforms (e.g.,eQMSsystems)
• Data-driven decision-maker who uses metrics to drive continuous improvement

Strategic Mindset

• Ability toanticipateregulatory trendsandcorporate needs,and proactively adapt systems and processes
• Strong business acumen with an understanding of howQuality enables innovation and market success

Collaboration & Communication

• Excellent cross-functional collaboration skills, with the ability to translate complex regulatory requirements into practical, business-friendly solutions
• Clear and compelling communicator, capable of engaging audiences from frontline teams to executive leadership

What you’llget:

• A front row seat tolife changingCGM technology.[_Learn about our brave #dexcomwarriors community_](https://www.dexcom.com/warriors).
• A full andcomprehensive benefitsprogram.
• Growth opportunities on a global scale.
• Access tocareer development through in-house learning programs and/orqualifiedtuition reimbursement.
• Anexcitingandinnovative,industry-leading organizationcommitted to our employees,customers, and the communities we serve.

Travel Required:

• 15-25%

Experience and Education Requirements:

• Typically requires a Bachelor’s degree with 17+ years of industry experience
• 13+ years of years of successful leadership experience in relevant industry

Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com.

If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at talentacquisition@dexcom.com.

Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided: [https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true](https://protect-us.mimecast.com/s/fufTCyPOPqFWlgBzhMXJ2t?domain=health1.meritain.com)

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