R

Resmed

Cloud-connected medical devices and software platforms

Compliance Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSan Diego, CA, USA$91k - $113kIn-person

About the Job

Requirements

  • A Bachelor of Science or Master of Science in any engineering discipline is required; Computer Science is preferred.
  • Working knowledge of regulations including MDSAP, ISO 13485:2016, IEC 62304, and SOC 2 controls.
  • Three years of experience delivering medical products and navigating audits such as MDR, SOC 2, MDSAP, HDS, or another regulatory framework is a plus.
  • Proficiency in report writing, analysis, and compliance procedures.
  • Thorough understanding of regulatory frameworks.
  • Solid technical knowledge and understanding of the Software Product Life Cycle (SDLC).
  • No hands-on coding experience is needed.

Responsibilities

  • Act as the subject matter expert for audits of the company's digital products and represent Engineering in audits, including HDS, MDSAP, SOC 2, and MDR.
  • Identify and evaluate technical design alternatives to achieve desired functionality in partnership with cross-functional team members and Systems Architecture Leaders.
  • Educate engineering teams on design review needs, facilitate the design review process, enhance or modify existing design review processes, and help resolve technical issues.
  • Drive the bug-triage process and help determine issues that impact patient safety.
  • Participate in product roadmaps and influence feature releases based on safety risk analysis.
  • Bridge Product Engineering and Quality/Regulatory teams, sharing knowledge of the latest safety-related standards.
  • Apply regulatory knowledge to challenging problems with implications for regulatory requirements around the world.
  • Ensure technical compliance with applicable laws and regulations.
  • Research and identify applicable regulatory and industry compliance standards and codes.
  • Collaborate with engineers and designers to deliver compliant products and services.
  • Ensure products achieve performance, functionality, and reliability as specified in marketing and systems specification documents.
  • Act as the subject matter expert for formal releases and ensure required compliance and regulatory deployment documentation is complete.
  • Prepare compliance reports by collecting, analyzing, and summarizing measurement data and trends related to post-launch market data.

Desired Qualifications

  • Computer Science is the preferred degree discipline.
  • Three years of experience delivering medical products and navigating audits such as MDR, SOC 2, MDSAP, HDS, or another regulatory framework is a plus.

About the Company

Resmed

Cloud-connected medical devices and software platforms

ResMed creates cloud-connected medical devices and software platforms to treat and manage sleep apnea, COPD, and other chronic diseases. Its devices (like sleep therapy gear) collect patient data and deliver therapy, while connected software platforms enable remote monitoring, coaching, and caregiver support. The company sells medical devices and offers software subscriptions, generating revenue from product sales and ongoing service fees. Unlike some competitors, ResMed combines hardware with cloud-based analytics and a broad ecosystem that supports patients, healthcare professionals, and caregivers across more than 120 countries. Its goal is to improve patient care and quality of life while reducing hospital visits and overall healthcare costs.

Company size
5,001-10,000
Company stage
IPO
Headquarters
San Diego, CA
Founded
1989

Recently Posted Jobs

Explore more opportunities at Resmed

See more jobs