Staff Systems Engineer HW Platform

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 were 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 weve 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. Weve already changed millions of lives and were 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. Well get there by constantly reinventing unique biosensing-technology experiences. Though weve 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:

Join the foundational engineering team that is shaping the future of continuous sensing at Dexcom. As a Staff Systems Engineer on our Systems Engineering team you will be at the epicenter of our next-generation product strategy. Our work enables product teams to innovate faster and more reliably than ever before. If you are passionate about architecting core technology defining clean interfaces and driving a design-once use-many philosophy in a regulated medical device environment this is the team for you.

Where you come in:

• You will be the primary Systems Engineering lead for defining the architecture and requirements for reusable hardware platforms translating high-level business and user needs into a verifiable set of design inputs.

• You will create and own the golden source Platform Requirements and the Platform Architecture Document in Jama Connect establishing the technical baseline for all consuming product teams.

• You will meticulously define and document the external interfaces of the platform creating a stable and unambiguous contract for product development teams to build against.

• You will collaborate deeply with hardware (EE/ME) firmware sensor QA RA and V&V teams to decompose system-level performance targets into allocated budgets for power timing and other Key Performance Parameters (KPPs).

• You will lead the formal decomposition of system-level hazards into platform-specific technical failure modes authoring the Platform FMEA that serves as a critical reusable input for all product-level safety risk assessments.

• You will champion the platform methodology providing expert guidance to consuming product teams on how to correctly reuse requirements incorporate design evidence by reference and manage the lifecycle of a platform-based product.

• You will partner with V&V leads to create comprehensive Platform Verification Plans ensuring that test strategies are designed to produce a robust reusable Evidence Package for the Platform DHF.

• You will drive the technical trade-off analyses and design decisions that balance the competing needs of multiple product lines ensuring the platform architecture is robust and flexible enough to support the long-term product roadmap.

What makes you successful:

• You possess a deep first-principles understanding of electromechanical systems including analog/digital electronics power management RF communication (especially BLE) and mechanical design for high-volume manufacturing.

• You are an expert in top-down Systems decomposition capable of translating high-level needs into a hierarchy of verifiable requirements and architectural blocks and are proficient with tools like Jama Connect.

• You think in terms of interfaces contracts and reusable assets instinctively understanding how to create a black box subsystem that other teams can build upon with confidence.

• You have proven experience in medical device development under a formal design control process (e.g. 21 CFR 820.30) and a strong understanding of relevant standards like IEC and ISO 14971.

• You are a master of technical communication able to author clear unambiguous requirements documents and effectively articulate complex architectural concepts to cross-functional engineering and program leadership.

• You have a demonstrated ability to perform and lead technical risk assessments with experience in methodologies like FMEA.

• You thrive on collaboration and are skilled at influencing other senior engineers providing guidance and building consensus on complex technical trade-offs.

Nice to haves:

• You have direct experience with Product Line Engineering (PLE) methodologies or have worked on a platform-based development model in a regulated industry.

• You have an INCOSE Certified Systems Engineering Professional (CSEP) certification.

• You have hands-on experience with sensor technology low-power system design or wireless communication protocols.

• You have experience with the design and verification of sterile single-use medical devices.

What youll 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 in-house learning programs and/or qualified tuition reimbursement.

• An exciting and innovative industry-leading organization committed to our employees customers and the communities we serve.

Travel Required:

• 0-5%

Experience and Education Requirements:

• Typically requires a Bachelors degreein a technical discipline and a minimumof 8-12 years related experience orMasters degree and 5-7 yearsequivalent industry experience or a PhDand 2-4 years of experience.

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. Dexcoms AAP may be viewed upon request by contacting Talent Acquisition at

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

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: all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

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