Hinge Health logo

Senior Design Quality Engineer

Hinge Health

San Francisco, CA · HybridFull-time$156–215K/yrPosted 5 days agoStill listed 4 days ago

Most applications go out cold — see where you stand first. No sign-up to start.

Watch jobs like this.

Don't just apply. Show up ready.

Olive works from this exact posting.

At a glance

Compensation
$156–215K/yr
Location
San Francisco, CAHybrid
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Senior Design Quality Engineer will guide design quality across Hinge Health hardware product development, from early concept through commercialization and design transfer. The role partners with cross-functional teams to apply design controls, risk management, verification and validation, reliability, and process validation while supporting patient safety, product quality, and compliance. It also drives quality readiness, supports regulatory activities, and improves quality practices as the medical-device organization scales.

Skills & qualifications

RequiredNice to have

Skills

Design ControlsRisk ManagementElectromechanical SystemsISO 13485ISO 14971IEC 60601IEC 6230421 CFR Part 820Software as a Medical DeviceSoftware in a Medical DeviceQuality Management SystemsConsensus BuildingData AnalysisProtocol DevelopmentReliabilityDesign for QualityExecutive Communication

Qualifications

Bachelor's in Engineering or Related6+ Years Quality Engineering Experience4+ Years Medical Device Design Experience3+ Years Design Controls and Risk Management ExperienceAdvanced Engineering DegreeSaMD or SiMD ExperienceQuality Management System ExperienceCoaching or Mentoring Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Tuition Assistance

Full job description

About the role Join Hinge Health’s Hardware organization and help build safe, reliable, scalable healthcare products that improve how people move beyond pain. As a Sr Design Quality Engineer, you’ll be a core member of cross-functional product development teams, guiding design quality from early concept through commercialization and design transfer.

You’ll bring practical expertise in design controls, risk management, verification and validation, reliability, manufacturability, product development lifecycle activities, and process validation. You’ll partner closely with engineering, product, manufacturing, purchasing, test, supplier engineering, and Regulatory Affairs to help teams move quickly without compromising patient safety, product quality, or compliance.

What You’ll Accomplish In your first 3 months

  • Build working knowledge of Hinge Health’s quality management system, product development lifecycle, tools, and design-quality practices.

  • Establish trusted partnerships with hardware, software, systems, product, program management, and Regulatory Affairs stakeholders.

  • Join active product development programs and begin reviewing requirements, design records, risk documentation, and development plans for quality and compliance gaps.

In your first 6 months

  • Own or materially contribute to design-control and risk-management execution across product development programs, from user needs and design inputs through design outputs, verification, validation, and transfer.

  • Help teams create and maintain complete, accurate, traceable, and inspection-ready design history file records.

  • Develop and review risk-based verification and validation strategies, including protocols, reports, acceptance criteria, traceability, and objective evidence.

  • Provide actionable quality feedback on design architectures, component selections, requirements, drawings, interfaces, usability and human-factors considerations, and risk controls.

In your first year

  • Drive quality readiness for design transfer and commercialization by partnering with manufacturing, purchasing, test, and supplier engineering on scalable designs, process validation, production readiness, and configuration control.

  • Lead or support product risk-management activities covering user, design, process, supplier, and software-enabled product risks, and help teams make balanced decisions that protect patient safety.

  • Support Regulatory Affairs with submissions, responses to regulatory questions, and audit preparation, participation, response development, and follow-up.

  • Coach and influence engineering teams on design quality, design controls, risk management, data analysis, protocol development, reliability, and design-for-quality methods.

  • Identify and implement practical improvements to quality workflows, templates, instructions, and cross-functional ways of working as Hinge Health scales its medical-device product organization.

Who You Are

  • A quality engineering subject matter expert who can guide cross-functional teams through complex, regulated product development and commercialization activities.

  • A risk-based decision maker who protects patient safety and product quality while thoughtfully balancing schedule, cost, technical, and business constraints.

  • An owner who solves complex problems with minimal oversight, follows issues through to resolution, and escalates risks that could affect safety, compliance, or launch readiness.

  • A clear communicator who can translate complex technical, quality, and regulatory information for engineers, cross-functional partners, and executive stakeholders.

  • A collaborative coach who makes design quality practical and relevant, helping teams adopt strong practices without relying solely on authority or procedure.

  • A Learn-it-all who stays curious about evolving medical-device standards, software-enabled products, reliability methods, and better ways to scale quality.

Basic Qualifications

  • Bachelor’s degree in electrical engineering, mechanical engineering, systems engineering, mathematics, physics, or a related technical field.

  • 6+ years of experience in quality engineering or a related field, including at least 4 years in a medical-device design and development environment.

  • 3+ years of experience applying design controls and risk management from early design and development through commercialization, including experience with electromechanical systems and applicable medical-device standards such as ISO 13485, ISO 14971, IEC 60601, IEC 62304, and 21 CFR Part 820.

Preferred Qualifications

  • Advanced degree in engineering, mathematics, physics, or a related technical field.

  • Experience with software as a medical device (SaMD) and software in a medical device (SiMD).

  • Experience navigating a quality management system with minimal oversight across individual product development projects.

  • Demonstrated ability to make balanced risk decisions, build consensus, and work through complex technical challenges.

  • Experience coaching, mentoring, or teaching engineering teams in design quality, data analysis, protocol development, reliability, or design-for-quality methods.

  • Experience communicating complex quality, technical, and regulatory information to executive management.

Hinge Health Hybrid Model This is a hybrid role based in the San Francisco office, requiring in-person attendance three days per week, for the full 8 hours of a typical business day. The San Francisco office has a dog-friendly workplace program. About Hinge Health At Hinge Health, we’re using technology to scale and automate the delivery of healthcare, starting with musculoskeletal (MSK) conditions, which affect over 1.7 billion people worldwide.

With an AI-powered human-centered care model, Hinge Health leverages cutting-edge technology to improve outcomes, experiences, and costs to help people move beyond their pain. The platform addresses a broad spectrum of MSK care, from acute injury to chronic pain to post-surgical rehabilitation, through personalized, evidence-based care.

As the preferred partner to 60+ health plans, PBMs, and other ecosystem partners, Hinge Health is available to over 20 million people across more than 2,800 employers. The company is headquartered in San Francisco, with additional offices in Montreal and Bangalore.

Learn more at hingehealth.com. What You’ll Love About Us

  • Inclusive healthcare and benefits: On top of comprehensive medical, dental, and vision coverage, we offer employees and their family members help with gender-affirming care, tools for family and fertility planning, and travel reimbursements if healthcare isn’t available where you live.

  • Planning for the future: Start saving for the future with our traditional or Roth 401(k) retirement plan options, which include a 2% company match.

  • Modern life stipends: Manage your own learning and development.

  • Grow with us: Grow with us through discounted company stock through our ESPP with easy payroll deductions.

Culture & Engagement Hinge Health is an equal opportunity employer and prohibits discrimination and harassment of any kind.

We make employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability status, pregnancy, or any other basis protected by federal, state, or local law.

We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

We provide reasonable accommodations for candidates with disabilities. If you feel you need assistance or an accommodation due to a disability, let us know by reaching out to your recruiter.

By submitting your application, you are acknowledging that we are using your personal data as outlined in the personnel and candidate privacy policy.

Beware of Phishing Attempts: We've noticed an increase in phishing where fraudsters impersonate employees and send fake job offers to steal sensitive information. We'll never ask for financial details during the hiring process and only use "@hingehealth.com" emails. If you receive a suspicious offer, stop communication and report it to the US FBI Internet Crime Complaint Center. To verify an email from our recruiting team, forward it to [email protected].

How this job compares

Set against the 3,022 open Quality Engineer jobs on Olive Jobs, counted October 29, 2026.

Pay
  • This posting$156–215K/yr
  • California median$111–164K/yr332 salary ranges
  • US median$90–149K/yr1,915 salary ranges

This range's midpoint, $185K, is 35% above the California median midpoint ($138K) — in the top quarter of Quality Engineer salary ranges in California.

Openings
Olive Jobs lists 412 open Quality Engineer jobs in California and 3,022 across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most in California
Experience
This posting asks for at least 6 years of experience — more than three in four Quality Engineer postings that state a minimum ask for (median 5 years, across 2,472 postings).
Education
This posting asks for a bachelor's degree; 1,735 of the 3,022 open Quality Engineer jobs (57%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on October 29, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

Similar jobs, posted recently

Open roles like this one, listed in the last 30 days.

You've read the whole posting — now see how you match it.