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Sr. Quality Engineer - Corrective & Preventive Actions

iRhythm Technologies, Inc.

United States

Remote

USD 96,000 - 125,000

Full time

4 days ago
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Job summary

Join iRhythm Technologies, a key player in digital healthcare, as a Senior Quality Engineer for Corrective & Preventive Actions. In this role, you'll drive compliance and continuous improvement initiatives. Be part of a dynamic team, ensuring high-quality standards are met in an innovative environment focused on cardiac health solutions.

Benefits

Medical, dental, and vision insurances
401(k) with company match
Unlimited LinkedIn Learning classes
Paid parental leave
Emotional health support

Qualifications

  • Minimum of 5 years in Quality or Regulatory roles.
  • 3 years of experience with CAPA in medical device companies.
  • Deep understanding of CAPA Regulatory requirements.

Responsibilities

  • Ensure CAPA system compliance with relevant standards.
  • Train and mentor CAPA owners on best practices.
  • Engage in continuous improvement of CAPA program.

Skills

Project Management
Problem-Solving
Investigational Skills
Attention to Detail

Education

Bachelor's Degree

Job description

Sr. Quality Engineer - Corrective & Preventive Actions

Join to apply for the Sr. Quality Engineer - Corrective & Preventive Actions role at iRhythm Technologies, Inc.

Sr. Quality Engineer - Corrective & Preventive Actions

Join to apply for the Sr. Quality Engineer - Corrective & Preventive Actions role at iRhythm Technologies, Inc.

Get AI-powered advice on this job and more exclusive features.

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

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

About This Role:

Boldly innovating to create trusted solutions that detect, predict, and prevent disease.

Discover your power to innovate while making a difference in patients' lives. iRhythm is advancing cardiac care…Join Us Now!

At iRhythm, we are dedicated, self-motivated, and driven to do the right thing for our patients, clinicians, and coworkers. Our leadership is focused and committed to iRhythm’s employees and the mission of the company. We are better together, embrace change and help one another. We are Thinking Bigger and Moving Faster.

About This Role

As the Sr Quality Engineer - Corrective & Preventive Actions (CAPA), you will be responsible for maintaining a robust global CAPA process across iRhythm. You will serve as an advocate for cross functional collaboration, continuous improvement, and compliance, with the responsibility of driving excellent quality system CAPA process performance globally. This role will work closely with cross-functional CAPA owners to provide training, guidance, and review of CAPA investigations and phases. In this role you will have the opportunity to impact product and process quality and regulatory compliance at iRhythm.

Essential Duties And Responsibilities:

  • Ensure the CAPA system is compliant with U.S. and applicable international standards/regulations, including ISO 13485, ISO 14971, and EU MDR requirements.
  • Partner with CAPA owners and stakeholders on assessing issue descriptions and ensuring containment, root cause analysis, correction, corrective and preventive actions, and effectiveness checks are appropriate, robust, and timely.
  • Train and mentor CAPA owners in all required elements and best practices of CAPA, including use of the CAPA tool.
  • Represent CAPA program, system and individual CAPA records during regulatory and internal audits.
  • Maintain the quality and compliance of CAPA system records to ensure audit-readiness for internal and external quality system audits.
  • Engage in continuous improvement of the CAPA program by identifying opportunities and recommending actions.

About You

Experience and Minimum Qualifications:

  • Bachelor’s Degree or the equivalent quality/regulatory experience.
  • Minimum of 5 years of experience in a Quality or Regulatory related role.
  • Minimum of 3 years of experience with Corrective Action and Preventative Action activities, within a medical device or equivalent healthcare company.

Knowledge, Skills And Abilities:

  • Must have a deep understanding of the CAPA system and associated regulatory requirements.
  • Previous experience in a medical device with working knowledge of ISO 13485, FDA 21 CFR 820, European Union MDD/MDR.
  • Strong investigational and problem-solving skills.
  • Demonstrates Project Management abilities to lead and manage several projects, meet deadlines and use critical thinking skills to solve problems effectively.
  • Must build rapport across functional teams within the organization and have the ability to work comfortably at all levels within the organization.
  • Attention to detail and timeliness are critical
  • Basic statistical methods including trend analysis.

Work Environment / Other Requirements:

  • Work location - remote
  • This role supports various U.S. and UK iRhythm sites and may require 15% travel.

What’s In It For You:

This is a regular full-time position with competitive compensation package, excellent benefits including medical, dental, and vision insurances (all of which start on your first day), health savings account employer contributions (when enrolled in high deductible medical plan), cafeteria plan pre-taxed benefits (FSA, dependent care FSA, commute reimbursement accounts), travel reimbursement for medical care, noncontributory basic life insurance & short/ long term disability. Additionally, we offer:

  • emotional health support for you and your loved ones
  • legal / financial / identity theft/ pet and child referral assistance
  • paid parental leave, paid holidays, travel assistance for personal trips and PTO!

iRhythm also provides additional benefits including 401(k) (with company match), an Employee Stock Purchase Plan, pet insurance discount, unlimited amount of LinkedIn Learning classes and so much more!

FLSA Status: Exempt

As a part of our core values, we ensure a diverse and 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 taops@irhythmtech.com

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.

Location:

Remote - US

Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.

Estimated Pay Range

$96,000.00 - $125,000.00

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 taops@irhythmtech.com

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.

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Quality Assurance
  • Industries
    Medical Equipment Manufacturing

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