资深软件质量保证工程师
Staff SW QA Engineer
公司德克斯康公司 (NASDAQ DXCM) 是持续葡萄糖监测 (CGM) 的先驱和全球领导者。德克斯科开始作为一个小公司,有一个巨大的梦想:永远改变糖尿病管理方式。释放信息和见解来推动更好的健康结果。这里我们25年后,已经开拓了一个行业。我们刚刚开始了。我们正在扩大我们的视野超越糖尿病以使人们能够控制健康。这意味着个性化,可行的见解旨在解决重要健康挑战。继续我们所开始的:改善人类健康。我们是由全球数千名雄心勃勃,热情的人驱动的,他们愿意像战士一样奋斗,以赢得客户信任,通过倾听,诚实地服务,大思维和可靠性。我们已经改变了数百万人的生活,我们准备更改数百万人。我们的未来目标是成为一个领先的消费者健康技术公司,同时继续开发解决方案严重的健康状况。我们将不断重新发明独特的生物传感技术体验。尽管我们从小企业时代走过很长的路,但我们的梦想比以往任何时候都更大。在全球范围内改善健康的机会都在你面前。见到团队:为软件质量保证活动提供技术专业知识,包括 ISO 14971规范下的风险管理活动。支持开发和实施可扩展的质量系统,风险管理实践以及确保产品安全,有效性和监管合规性的软件合规策略。与高级研发工程,质量,监管,临床,网络安全及企业领导合作,推动 SDLC 持续改进和产品生命周期中优化质。影响组织质量战略并担任认可的软件质量的专家。你所在地:·你将担任软件质量,风险管理和软件生命周期合规活动的技术领导者和专家。·你将负责软件开发和 V&V 过程的有效应用,合规性和持续改进,包括:风险管理,I/II 类豁免应用程序与组件的软件设计控制。·你会领导复杂的软件质量的举措,涵盖多种产品,计划和功能组织。·你还将负责风险评估。
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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:
Provides technicalexpertisefor software quality assurance activities, including risk management activities following ISO 14971.Supportsthe development and implementation of scalable quality systems, risk management practices, and software compliance strategies that ensure product safety, effectiveness, and regulatory compliance. Partners with seniorR&Dengineering, quality, regulatory, clinical, cybersecurity, and business leaders to drive continuous improvements to SDLC, and quality excellence throughout the product lifecycle. Influences organizational quality strategy and serves as a recognized subject matter expert insoftware quality.
Where you come in:
- You will serve as a technical leader and subject matter expert for software quality, risk management, software lifecycle compliance activities.
- You will lead the effective application, compliance, and continuous improvement of software development andV&Vprocesses, including:Risk Management, Software Design Controls for Class I/II Exempt Applications & Components
- You will lead complex software quality initiatives spanning multiple products, programs, and functional organizations.
- You will lead risk assessments for software anomalies, cybersecurity vulnerabilities, emerging technologies, and post-market issues.
- You will supportdigital transformation initiatives (ALM, SCM, PLM) to evolve use of electronic systems supporting SDLC as definedperIEC62304.
- You will provide technical oversight and direction for software risk management activities, including DFMEA, PFMEA, SHA, and hazard analysis.
- You will review and approve critical quality deliverables, including software development lifecycle documentation, risk artifacts,V&Vprotocols, and design history file content.
- You will drive organizational improvements related to software quality systems, development practices, automation, verification, validation, and compliance processes.
- You will evaluate emerging regulations, standards, and industry trends and assess impacttoexisting and future products.
- You will collaborate with senior leadership to define quality strategies supporting businessobjectivesand product roadmaps, implementinga right-sized QMSapplications based on Software Classification per IEC62304.
- You will mentor and provide technical leadership to software quality engineers and cross-functional development teams.
- You will influence project, product, and organizational decisions through expert risk-based quality assessments and recommendations.
- You will assume and perform other duties as assigned.
What makes you successful:
- You have extensive medical deviceexperiencedemonstratedexpertisein FDA 21 CFR Part 820, IEC 62304, ISO 13485, ISO 14971, IEC 82304, EU MDR, and applicable global regulatory requirements.
- You have advancedknowledge of software development lifecycle processes and software development methodologies including Agile, Waterfall, DevOps, Continuous Integration, Continuous Delivery(CI/CD), and Test Automation.
- You have deep experience with software quality engineering across requirements, architecture, design, development, testing, release, and post-market activities.
- You have advanced understanding of software risk management principles, methodologies, and regulatory expectations.
- You have demonstrated ability to influence organizational direction and lead cross-functional initiatives without direct authority.
- You have strong understanding of software architectures, cloud technologies, distributed systems, cybersecurity principles, and data platforms.
- You have experience supporting regulatory inspections and direct interactions with FDA, notified bodies, and external auditors.
- You have exceptional written, verbal, and executive-level communication skills.
- You have the ability to manage ambiguity, influence senior stakeholders, and drive complex programs to successful completion.
- You have demonstratedsuccessmentoring engineers and developing organizational quality capabilities.
Whatyou’llget:
- A front row seat tolife changingCGM technology.Learn about our brave #dexcomwarriors community.
- Afull 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 in a technical discipline and a minimum of 8-12 years related experience or Master’s degree and 5-7 years equivalent industry experience or a PhD and 2-4 years of experience.
RemoteWorkplace:Your location will be a home office; youare not required tolive within commuting distance of your assigned Dexcom site (typically 75 miles/120km).If youresidewithin commuting distance of a Dexcom site (typically 75 miles/120km)a hybridworking environment may be available. Ask about our Flex workplaceoption.
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 .
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:
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.
AI in Hiring Notice: We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people.
Salary:
$116,600.00 - $194,400.00
#DexcomUS
Originally posted on Himalayas