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Salary
≈ $12k – $34k per year (Estimated)
Location
In office (Johor Bahru)
Seniority
Senior · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 29, 2026. First seen by Alion on Oct 29, 2026. ResMed scores B on the Alion truth index.

Overview
Company
Impact
Profile match
ResMed is a medical device company founded in Sydney in 1989 by a physician who had helped develop the first practical treatment for obstructive sleep apnoea and could not persuade anyone else to commercialise it. It makes the masks, flow generators and ventilators used to treat sleep apnoea and chronic respiratory disease, and it has built a large software business in the cloud platforms that manage those devices and the out-of-hospital care around them. Now headquartered in San Diego and listed in New York and Sydney, it shares the sleep apnoea market largely with Philips and benefited substantially from its competitor's device recall.
Backed by Hikma Ventures

About the Role

We are seeking a highly motivated QA Engineer, Post Market Quality to support post-market quality activities and ensure the continued safety, performance, and compliance of products in the field. This role will work closely with cross-functional teams, including R&D, Regulatory Affairs, Service Operations, Manufacturing, and Customer Quality, to investigate product issues, drive corrective actions, and maintain compliance with applicable quality and regulatory requirements.

The successful candidate will play a key role in complaint handling, product failure investigations, trend analysis, quality system improvements, and post-market surveillance activities to support continuous improvement and customer satisfaction.

Key Responsibilities

Complaint Handling & Investigations

  • Review, assess, and manage customer complaints in accordance with internal procedures and regulatory requirements.
  • Lead or support investigations into product quality issues, field failures, and customer-reported concerns.
  • Perform root cause analysis and ensure timely implementation of corrective and preventive actions (CAPA).
  • Prepare investigation reports and support regulatory reporting activities where required.

Post-Market Surveillance & Trend Analysis

  • Analyze complaint, service, and field performance data to identify trends, recurring issues, and emerging risks.
  • Recommend improvements and corrective actions based on data-driven insights.
  • Monitor product performance and collaborate with stakeholders to drive continuous improvement initiatives.

Quality Systems & Compliance

  • Support the implementation, maintenance, and continuous improvement of post-market quality processes and procedures.
  • Ensure compliance with applicable quality standards, regulatory requirements, and internal policies.
  • Participate in internal and external audits and support audit readiness activities.
  • Maintain documentation in accordance with quality system requirements.

Cross-Functional Collaboration

  • Work closely with R&D teams to provide feedback on field performance and quality-related design improvements.
  • Partner with Regulatory Affairs, Manufacturing, Service, and Customer Support teams to ensure timely resolution of quality issues.
  • Support new product introductions by providing quality and post-market perspectives during product development activities.

Continuous Improvement

  • Identify opportunities to enhance complaint handling, investigation effectiveness, and overall quality system performance.
  • Participate in quality improvement projects and process optimization initiatives.
  • Support the development of service tools, manuals, and post-market service documentation where applicable.

Qualifications

Required

  • Bachelor's Degree in Engineering, Quality, Life Sciences, Manufacturing, or a related discipline.
  • Minimum 5 years of experience in Quality Engineering, Quality Assurance, Post Market Quality, Customer Quality, or a similar function.
  • Experience with complaint handling, investigations, root cause analysis, and CAPA activities.
  • Strong analytical and problem-solving skills.
  • Excellent communication and stakeholder management skills.
  • Ability to work effectively in a cross-functional and global environment.

Preferred

  • Experience in the Medical Device, Healthcare, Pharmaceutical, or other highly regulated industries.
  • Working knowledge of quality management systems and regulatory requirements.
  • Experience conducting data analysis and identifying quality trends.
  • Familiarity with ISO standards, GMP requirements, and post-market surveillance activities.
  • Experience collaborating with product development and engineering teams.
  • Exposure to AI, automation, or advanced data analytics tools used to support complaint investigations, trend analysis, root cause identification, or continuous quality improvement is considered a strong advantage.

Success in This Role

The successful candidate will:

  • Drive timely and effective resolution of customer complaints and product quality issues.
  • Ensure compliance with quality system and regulatory requirements.
  • Proactively identify trends and recommend improvements to enhance product quality and customer satisfaction.
  • Build strong partnerships with cross-functional teams and contribute to continuous improvement initiatives.
  • Serve as a trusted quality partner throughout the product lifecycle.

Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now!

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