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iRhythm Technologies is hiring a Supervisor, Post Market Complaints

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Job Description

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

iRhythm Technologies, Inc. is looking for a Supervisor, Quality Assurance to join the Quality team. The Supervisor will oversee the Post Market Complaints and Document Management team to ensure compliance, accuracy, and efficiency. The Supervisor will provide instruction and feedback to the team as needed. The position will also provide data and analysis to support Quality department as needed.

Our work environment is a fast-paced atmosphere, fostering excellent cross-functional collaboration. Most of all, we are passionate about delivering innovations that improve the quality of health care and the patient experience. We are looking for like-minded individuals who are quality driven and patient focused to join our team!

Responsibilities

  • Provide supervision and leadership to team of Complaint Investigators
  • Manage and balance assignment of work to team to meet goals.
  • Provide guidance, development and performance feedback and opportunities for growth through regular one-one-one and team meetings.
  • Annual Performance reviews with quarterly check-ins
  • Review investigated complaints to ensure procedural and regulatory compliance.
  • Manages and responds to regulatory body inquiries relating to reported complaints.
  • Ensures documents are managed in a timely manner, ensuring all procedural requirements are met.
  • Ensures complaints are closed in a timely manner, ensures all global medical device reports are submitted within regulatory timeframes.
  • Participates in process improvements to improve compliance, effectiveness, and efficiency.
  • Perform other quality and regulatory-related duties as assigned.

Required Qualifications:

  • Bachelor’s Degree or Associate Degree in science, technology, or medical fields
  • 5+ years of experience in Quality Assurance and / or a complaint processing role, experience with Medical Device Reporting.
  • Supervisory or Lead experience in a medical device company
  • Strong working knowledge of ISO 13485, FDA 21 CFR 820, European Union MDD /MDR
  • Strong interpersonal and organizational skills to enable working cross-functionally within the organization,
  • Strong problem-solving skills, critical-thinker, and experience at investigating and resolving complex issues.
  • Understand basic principles of good technical writing skills and be able to articulate findings and formulate conclusions.
  • Identify problems and lead projects to improve processes, procedures and/or practices; recommend and resolve solutions.
  • Excellent communication (verbal and written) and interpersonal skills required.
  • Demonstrated experience with MS Word, Excel, Adobe Acrobat, and other commonly used software systems.
  • Must be able to work under minimum supervision and in a team environment.

What's In It For You

iRhythm GBS Philippines is committed to providing an exciting career path for every team member, with unlimited learning opportunities for you. Our key focus is to ensure a healthy and well-balanced work life, which is why we provide you with comprehensive health and life insurance benefits, with eligible dependent coverage. We offer a competitive compensation package and above industry standard paid leave benefits. 

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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.

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Salary Information

Salary: $40,000 - $60,000

🤖 This salary estimate is calculated by AI based on the job title, location, company, and market data. Use this as a guide for salary expectations or negotiations. The actual salary may vary based on your experience, qualifications, and company policies.

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