Software QA Engineer 2

This functional department provides technical support and guidance to the Software teams to ensure conformance to software development process and applicable safety and quality system regulation and standards such as IEC 62304, ISO 13485, ISO 14971, 21 CFR 820. Weare responsible forvarious aspects of Software Design Assurance withfocuson product improvement, new productdevelopmentand defect prevention. Weinterface withdifferent cross functional groups (Software Engineering, Software Test, Regulatory Affairs, Marketing, Project management, System Engineering, Clinical and others). This team hasa great teamculturebysupporting each other in a fast-paced environment and dealing with shifting priorities with a positive attitude.

Where you come in:

• You will activelyparticipateas a core team member of the R&D Quality Assurance Engineering team

• You will provide guidance on IEC 62304, 21 CFR 820,ISO14971and other relevant regulations worldwide to the cross-functional teams

• You will lead in the effective application, compliance, and continuous improvement of policies, procedures, and practices related to software development and validation across software teams

• You willprovidetechnical guidance with respect to equipment, software, product, process requirements and driving risk management deliverables like SHA,designand process FMEA

• You will provide guidance to Software Design and Test Teams for System validations, Software design verification and traceability, Software configuration management, tool vali-dations and software integrations.

• You will support post market activities related to Software anomalies, riskassessmentsand CAPA activities (if applicable)

• Youare responsible forreviewing, authoring, revising, and approvingappropriate technicaldocumentation including design history file, standard operating procedures, protocols, reports, and software design control deliverables

• You will assess impact of change control to ensure no adverse impact to product performance and a state of compliance is maintained

• You will effectively communicate with broad Dexcom team and upper-level management on plans, status of tasks, projectprogressand challenges

• You will assume and perform other duties as assigned, To 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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• You have experience working with software mobile applications

• You bring Medical Device experience in compliance with the requirements of FDA 21 CFR Part 820, IEC 62304, ISO13485and ISO 14971

• Your knowledge and experience with SDLC processes along with software development methodologies such as Agile Software Development, Waterfall Model

• Your Software Quality or Engineering experience in Requirements Analysis, Design/Development, Product Integration and Test

• Yourproficiencyto interpret software design and code to verify implementation of requirements

• You have Software development and/or Software test experience.

• Your ability to understand complex tasks and goals.Drive projects to completion with limited supervision.

• Your ability to communicate and present to all levels of management

• Nice to haveknowledge ofCyber Security

• Nice to have ASQ Certified Software Quality Engineer (CSQE) certificationor equivalent

• Nice to have Jama, Jira,Kettryx,and/orTest Railsexperience, * Typically requires a Bachelor’s degree in a technical discipline, and a minimum of 2 - 5 years related experience or Master’s degree and 0-2 years’ equivalent experience.

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.