I

iRhythm Technologies

Wearable cardiac monitoring with data analysis

Post Market Complaint Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeManila, Metro Manila, PhilippinesNo salary listed

About the Job

Requirements

  • A bachelor's degree or associate degree in a science, technology, or medical field.
  • Three to five years of experience in Quality Assurance and/or complaint processing.
  • Strong problem-solving and critical-thinking abilities, with experience investigating and resolving complex issues.
  • Understanding of basic technical-writing principles and the ability to articulate findings and formulate conclusions.
  • Ability to work across functional teams and seek input from Product Quality, Product Development Engineers, and other departments for complaint investigations.
  • Ability to work under minimum supervision and in a team environment.
  • Excellent verbal and written communication and interpersonal skills.
  • Demonstrated experience with Microsoft Word, Excel, Adobe Acrobat, and other commonly used software systems.
  • Ability to work at the office initially, shifting to hybrid once 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 closely with other departments to complete investigation reports.
  • Evaluate 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.
  • Identify problems and lead projects to improve processes, procedures, and/or practices; recommend and resolve solutions.
  • Perform other quality- and regulatory-related duties as assigned.

Desired Qualifications

  • Previous medical-device experience with working knowledge of ISO 13485, FDA 21 CFR 820, and European Union MDD/MDR.
  • Basic knowledge of Quality Systems (CAPA/non-conformances/SCARS).
  • Experience with software/firmware complaints.

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

Recently Posted Jobs

Explore more opportunities at iRhythm Technologies

See more jobs