ZipRecruiter

Log In

1

Medical Device Software Quality Engineer Jobs (NOW HIRING)

Eightelevengroup

Software Quality Engineer

Warsaw, IN · On-site

$55 - $64/hr

Software Quality Engineer Warsaw, IN Hybrid role (3 days in office) $55 - $64 per hour ABOUT THE ... Support the design, development, and testing of medical device software, including Software as a ...

Brooksource

Software Quality Engineer

Indianapolis, IN · On-site

$55 - $64/hr

Software Quality Engineer Warsaw, IN Hybrid role (3 days in office) $55 - $64 per hour ABOUT THE ... Support the design, development, and testing of medical device software, including Software as a ...

Epia Neuro

Senior Quality Engineer

Alameda, CA · On-site

$102K - $139K/yr

Experience contributing to risk management (ISO 14971) processes within the scope of medical device software. * Comfortable raising quality concerns directly with engineering teams and holding a ...

Philips

Software Design Quality Engineer

Bedford, MA · On-site

$102K - $163K/yr

Job Title Software Design Quality Engineer The Software Design Quality Engineer is responsible for ... Track and risk assess software Anomalies for pre- and post-market medical device software.

Philips

Software Design Quality Engineer

Bedford, MA · On-site

$102K - $163K/yr

Job TitleSoftware Design Quality Engineer The Software Design Quality Engineer is responsible for ... Track and risk assess software Anomalies for pre- and post-market medical device software.

Philips

Software Design Quality Engineer

Bedford, MA · On-site

$102K - $163K/yr

Job Title Software Design Quality Engineer The Software Design Quality Engineer is responsible for ... Track and risk assess software Anomalies for pre- and post-market medical device software.

Philips

Software Design Quality Engineer

Bedford, MA

$102K - $163K/yr

Job TitleSoftware Design Quality Engineer The Software Design Quality Engineer is responsible for ... Track and risk assess software Anomalies for pre- and post-market medical device software.

Heartflow

Senior Device Quality Engineer

San Francisco, CA · Hybrid

$160K - $180K/yr

... Software as a Medical Device (SaMD) and AI/ML-enabled technologies-are safe, secure, and compliant ... ASQ Certified Quality Engineer (CQE), Certified Software Quality Engineer (CSQE), or Green Belt.

next page

Showing results 1-20

All JobsMedical Device Software Quality Engineer Jobs

Medical Device Software Quality Engineer information

See salary details

$18

$48

$78

How much do medical device software quality engineer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for medical device software quality engineer in the United States is $48.54, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $55.53 per hour, depending on experience, location, and employer.

What are popular job titles related to Medical Device Software Quality Engineer jobs?

For Medical Device Software Quality Engineer jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Software Quality Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $100,970 per year, or $48.5 per hour.

Software Quality Engineer

Warsaw, IN • On-site

Eightelevengroup
See more jobs at Eightelevengroupexternal

$55 - $64/hr

Other

Posted 22 days ago

Key responsibilities

  • Support the design, development, and testing of medical device software, including Software as a Medical Device (SaMD) products

  • Review test case execution results and manage software defects

  • Facilitate software risk assessment sessions and own the development of risk documentation

Job description

Software Quality Engineer

Warsaw, IN

Hybrid role (3 days in office)

$55 - $64 per hour

ABOUT THE ROLE

Join a Fortune 50 Life Sciences company as a Software Quality Engineer, providing quality leadership for a new product project team focused on the development of medical device software systems. In this hybrid role based in Warsaw, IN, you will serve as the subject matter expert in requirements gathering, software risk assessments, test strategy definition, and guiding the team on design controls and defect analysis. You will partner closely with R&D throughout the full development lifecycle—from upstream requirements and risk through mid-stream verification to ongoing compliance and audit readiness. This is a high-visibility opportunity to own quality end-to-end, gain exposure to a full medical device software toolchain, and collaborate cross-functionally with business partners and mentors.

WHAT YOU'LL DO
  • Support the design, development, and testing of medical device software, including Software as a Medical Device (SaMD) products
  • Provide leadership, guidance, and expertise on software development processes, procedures, and practices
  • Serve as a subject matter expert in requirements gathering, test strategy definition, and design controls
  • Facilitate documentation and tracking of verification activities, including code review findings
  • Review test case execution results and manage software defects
  • Facilitate software risk assessment sessions and own the development of risk documentation
  • Support regulatory filings and registrations, including 510(k) submissions and Design History File (DHF) creation
  • Provide technical support for audits of software suppliers and consultants, including cybersecurity and threat modeling topics
  • Conduct training on medical device software development processes and quality systems; develop associated work instructions
  • Provide expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance, FDA Part 11, ISO 13485, EU MDR, ISO 14971, IEC 62366, ISO 27001, HIPAA)
  • Collaborate closely with R&D and cross-functional teams to ensure compliance with industry standards and regulatory requirements
WHAT YOU BRING
  • Bachelor's degree or university degree in Engineering, Computer Science, Information Systems, or Biomedical/Bio-engineering (required)
  • Minimum 4 years of regulated industry experience in quality, new product development, or manufacturing engineering
  • Experience in the medical device industry
  • Proficiency with quality tools, systems, and processes (e.g., Windchill, Polarion, ETQ)
  • Strong interpersonal, organizational, and verbal/written communication skills
  • Ability to work collaboratively in a team environment and demonstrate leadership
  • Ability to perform duties in accordance with company policies, procedures, and civil rights requirements
  • ASQ Certification as a Software Quality Engineer or equivalent (preferred)
  • Expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance, FDA Part 11, ISO 13485, EU MDR, ISO 14971, IEC 62366, ISO 27001, HIPAA)
  • Experience supporting regulatory filings and registrations (e.g., 510(k) submissions, DHF creation)
  • Ability to facilitate software risk assessments and develop risk documentation
WHAT'S IN IT FOR YOU
  • Opportunity to own quality end-to-end on a high-visibility project for a Fortune 50 Life Sciences company
  • Exposure to a full medical device software toolchain (Windchill, Polarion, ETQ) and hands-on involvement
  • Meaningful mentorship scope and cross-collaborative team and business partners
  • Hybrid work environment (3 days in office)
#J-18808-Ljbffr

Apply