Dexcom-posted 3 months ago
$75,200 - $125,300/Yr
Full-time
Hybrid • San Diego, CA
Computer and Electronic Product Manufacturing

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.

  • Provide technical guidance with respect to equipment, software, product, process requirements and driving risk management deliverables like SHA, design and process FMEA.
  • Analyze risk and apply effective risk management and/or risk-based quality guidance controlling risk, verifying risk controls, and maintaining risk management throughout the product lifecycle.
  • Coordinate with team members to update Risk Management File and other risk artifacts.
  • Perform risk evaluations associated with post market data, give guidance to risk evaluations for product development.
  • Support in finding quality improvements related to Risk Management processes.
  • Support post market activities related to Software anomalies, risk assessments and CAPA activities (if applicable).
  • Experience working with medical device software.
  • Medical Device experience in compliance with the requirements of FDA 21 CFR Part 820, IEC 62304, ISO 13485 and ISO 14971.
  • Experience with EU MDR.
  • Ability to understand complex tasks and goals.
  • Drive projects to completion with limited supervision.
  • Ability to communicate and present to all levels of management.
  • Cyber Security experience.
  • ASQ Certified Software Quality Engineer (CSQE) certification.
  • 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.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service