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iRhythm Technologies

Wearable cardiac monitoring with data analysis

Complaints Specialist

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeManila, Metro Manila, PhilippinesNo salary listed

About the Job

Requirements

  • A bachelor's or associate degree in a science, technology, or medical field is required.
  • Three to five years of experience in Quality Assurance and/or complaint processing is required.
  • Strong problem-solving and critical-thinking skills, including experience investigating and resolving complex issues, are required.
  • The role requires basic technical-writing skills and the ability to articulate findings and formulate conclusions.
  • The role requires working across functional teams and seeking input from Product Quality, Product Development Engineers, and other departments during complaint investigations.
  • The role requires identifying problems, leading projects to improve processes, procedures, or practices, and recommending and resolving solutions.
  • Excellent verbal and written communication and interpersonal skills are required.
  • Demonstrated experience with Microsoft Word, Microsoft Excel, Adobe Acrobat, and other commonly used software systems is required.
  • The role requires working with minimal supervision and in a team environment.
  • The role requires working in the office initially, with a shift to hybrid work after onboarding is complete.

Responsibilities

  • Evaluate complaints to determine reportability in accordance with 21 CFR Part 803 Medical Device Reporting, European Vigilance Reporting, and other applicable requirements.
  • Perform and/or coordinate complaint investigations and gather additional information, working with other departments to complete investigation reports.
  • Evaluate all information from a technical perspective to ensure appropriate analysis and investigation are complete.
  • Ensure issues are addressed and escalated in a timely manner.
  • Maintain the complaints log.
  • Participate in process improvements.
  • Perform other quality- and regulatory-related duties as assigned.

Desired Qualifications

  • Previous medical-device experience and working knowledge of ISO 13485, FDA 21 CFR 820, and European Union MDD/MDR are an asset.
  • Basic knowledge of Quality Systems, including CAPA, non-conformances, and SCARS, is a plus.
  • Experience with software/firmware complaints is a plus.

About the Company

iRhythm Technologies

Wearable cardiac monitoring with data analysis

iRhythm Technologies develops cardiac monitoring technology, led by the Zio Patch wearable for up to 14 days of continuous heart-rhythm tracking. The patch is worn by a patient to collect long-term data, which is then analyzed by iRhythm’s services to provide diagnostic insights to healthcare providers without requiring frequent in-person visits. Compared with competitors, it combines extended, non-intrusive monitoring with integrated data analysis to streamline clinician workflows and support telehealth, selling both devices and analysis services to providers. The goal is to improve detection of arrhythmias, enhance diagnostic accuracy, and make patient care and clinician workflows more efficient through scalable wearable monitoring and interpretation of the collected data.

Company size
1,001-5,000
Company stage
IPO
Headquarters
San Francisco, CA
Founded
2006

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