Post Market, Complaint Specialist

LocationManila, PH

Work modehybrid

Typefull-time

SeniorityMid

Experience3–5 yrs

Company size1,001–5,000 people

First seenOct 10, 2026 · 1d ago

Verified live1d ago

At a glanceSummarised by Seekless from the posting.

Bachelor's Degree or Associate Degree in science, technology, or medical fields

3-5 years of experience in Quality Assurance and/or a complaint processing role

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

Must work across functional teams within the organization

Identify problems and lead projects to improve processes, procedures and/or practices; recommend and resolve solutions

Excellent communication (verbal and written) and interpersonal skills

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

Must be a positive and energetic team player

Evaluates complaints to determine reportability in accordance with 21 CFR Part 803 Medical Device Reporting, European Vigilance Reporting, etc.

Previous experience in medical devices with working knowledge of ISO 13485, FDA 21 CFR 820, European Union MDD/MDR is an asset

Basic knowledge of Quality Systems (CAPA/non-conformances/SCARS) a plus

Experience with software/firmware complaints a plus

Must be able to work at office for near future, shifting to hybrid once onboarding is complete

Skills

MS Word

Excel

Adobe Acrobat

Career-defining. Life-changing.

About the company

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:

Responsibilities

What You’ll Be Doing:

• Duties in this role include:

• Evaluates complaints to determine reportability in accordance with 21 CFR Part 803 Medical Device Reporting, European Vigilance Reporting, etc. • Performs and/or coordinates complaint investigations and gathering of additional information, working closely with other departments to complete investigation reports

• Evaluate all information from a technical perspective to ensure appropriate analysis and investigation is complete

• Ensures issues are being addressed and escalated in a timely manner

• Maintains complaints log.

• Participates in process improvements.

• Perform other quality and regulatory-related duties as assigned.

Requirements

What You Need for this Position:

• Bachelor’s Degree or Associate Degree in science, technology, or medical fields

• 3- 5 years of experience in Quality Assurance and / or a complaint processing role.

• Previous experience in medical devices with working knowledge of ISO 13485, FDA 21 CFR 820, European Union MDD /MDR is an asset

• 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.

• Must work across functional teams within the organization and seek input from Product Quality, Product Development Engineers, and other departments for complaint investigation.

• 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.

• Basic knowledge of Quality Systems (CAPA/non-conformances/SCARS) a plus

• Must be able to work under minimum supervision and in a team environment.

• Must be a positive and energetic team player.

• Must be able to work at office for near future, shifting to hybrid once onboarding is complete.

• Experience with software/firmware complaints a plus

Location:

Manila

Legal

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]

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

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