
New · posted Oct 15
iRhythm · Medical Devices
Director, Design Quality
- Remote, US
- Remote
- Full-time
- Director
Open until filled
The role
Career-defining. Life-changing.
At iRhythm, you’ll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what’s possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career
The Director of Design Quality provides strategic and operational leadership for design quality across iRhythm’s hardware, firmware, software, connected-device, and AI-enabled product portfolio. The role leads Design Quality Engineering teams and partners closely with R&D, Product Management, Manufacturing, Regulatory, Clinical, and Quality functions to ensure products are developed, transferred, and maintained in compliance with global regulatory requirements. This leader serves as the organization’s design controls and risk management expert, strengthens quality systems and culture, uses post-market insights to prevent recurrence of quality issues, and ensures quality is integrated into business and product-development decisions.
Essential Duties and Responsibilities:
- Lead, develop, and resource Design Quality Engineering teams across hardware and software disciplines.
- Provide expert and leadership oversight of design controls, design transfer, risk management, verification and validation, human factors, and product lifecycle activities.
- Partner with cross-functional leaders to establish clear quality strategies, requirements, decision points, and escalation paths throughout product lifecycle.
- Improve design-related Quality Management System processes, metrics, and governance to increase both compliance and operational effectiveness.
- Apply complaint, field-performance, and post-market data to identify product risks, implement corrective improvements, and prevent recurrence in future designs.
- Represent Design Quality during FDA inspections, Notified Body audits, regulatory interactions, and executive management reviews.
- Ensure compliance with FDA requirements, including the Quality Management System Regulation (21 CFR Part 820) and applicable software and cybersecurity guidance; ISO 13485; ISO 14971; IEC 62304; IEC 82304; IEC 62366, EU MDR, and other applicable international regulations and standards.
- Build and nurture a collaborative, patient- and customer-focused quality culture while influencing organizational change.
- Recruit, coach, and develop high-performing leaders and teams, including succession planning and capability development.
- Provide clear, fact-based reporting to executive leadership on quality risks, performance, resources, and improvement priorities.
- Other assignments as directed by management.
- Other assignments as directed by management.
Experience and Minimum Qualifications:
- Minimum of 15 years of related experience with a Bachelor’s degree; Related experience includes medical/science/healthcare field; or equivalent.
- At least 5 years of experience in a management position with direct reports.
- Demonstrated expert-level knowledge of Design Controls, Critical-to-Quality strategies, Risk Management, Cybersecurity, etc.
- Demonstrated knowledge of mechanical, electrical and software engineering in the development of complex devices
- Demonstrated knowledge in Software development lifecycle, including familiarity with embedded software and firmware, applications software and analytics; knowledge of software quality for mobile device apps and remote installation is a plus
- Proven capacity to collaborate and build positive relationships and trust over time with cross-disciplinary audiences.
- Experience with AI based devices and/or SaMD and/or wearable medical devices preferred.
- Master’s or advanced degree preferred
What’s In It for You:
This is a full-time position with competitive compensation package, excellent benefits including medical, dental, and vision insurance (all of which start on your first day), paid holidays, and PTO!
iRhythm also provides additional benefits including 401K (with company match), an Employee Stock Purchase Plan, paid parental leave, pet insurance discount, Cultural Committee/Charity events, and so much more!
What you need
Pay and benefits
$182,000 – $237,000 a year
Employer providedEstimated Pay Range
$182,000.00 - $237,000.00
Medical, dental, and vision insurance from day one
Paid holidays and PTO
401(k) with company match
Employee Stock Purchase Plan
Paid parental leave
Pet insurance discount
Working conditions
Location
Remote - US
Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.
From the posting
About iRhythm
About iRhythm Technologies
iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm’s vision is to deliver better data, better insights, and better health for all.
Make iRhythm your path forward. Zio, the heart monitor that changed the game.
There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist. Please note that all open positions will always be shown here on the iRhythm Careers page, and all communications regarding the application, interview and hiring process will come from a @irhythmtech.com email address. Please check any communications to be sure they come directly from @irhythmtech.com email address. If you believe you have been the victim of an imposter or want to confirm that the person you are communicating with is legitimate, please contact [email protected]. Written offers of employment will be extended in a formal offer letter from an @irhythmtech.com email address ONLY.
For more information, see https://www.ftc.gov/business-guidance/blog/2023/01/taking-ploy-out-employment-scams and https://www.ic3.gov/Media/Y2020/PSA200121
Equal opportunity, accessibility and legal noticesiRhythm's statements, word for word
As a part of our core values, we ensure an inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws.
iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at [email protected]
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is level with the US median for Quality Assurance roles at this level.
This roleEmployer provided
Director roles in the US102 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $182,000 | — | $237,000 |
| All US (middle half) | $186,500 | $209,250 | $231,375 |
This role: iRhythm's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not iRhythm's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 24 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership9
- Quality systems and risk6
- Data and digital systems5
- GMP and compliance4
- Documentation and SOPs1
- Investigations and CAPA1
- Validation and qualification1
- Regulatory submissions1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- European UnionEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Risk management for medical devices
- IECIEC 62304(official source, opens in a new tab)Software life cycle processes for medical device software
Company hiring pulse
iRhythm on Regulatory Jobs
- 6
- Open roles
- 6
- Distinct roles
- 3
- Locations
By discipline
- Quality5 83%
- Regulatory1 17%
By level
- Manager2 33%
- Senior & Principal2 33%
- Director1 17%
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Director, Design Quality at iRhythm
Open until filled. $182K–$237K a year, employer provided.

