Job Description

About Myant:

At Myant, our mission is to help people Live Younger, Longer by transforming healthcare from episodic, reactive care to proactive, preventive health management. Through our pioneering connected textiles and continuous monitoring technology, we bridge the gap between individuals, their families, and healthcare providers, creating a world where quality healthcare is more accessible, personalized, and preventative.

Powered by extensive, multidisciplinary R&D, Myant combines expertise in textile science and computing, biometrics, AI, and clinical research to develop technologies that seamlessly integrate into everyday life. Our innovation engine continuously expands the platform’s capabilities, addressing cardiovascular health, stress management, sleep optimization, and more.

With global ambitions, Myant is building a worldwide presence, collaborating with healthcare systems, clinics, researchers, and partners to set a new standard in connected health. Our goal is not just to improve care, but to fundamentally redefine the relationship people have with their health, shifting the focus from sick care to lifelong wellness.

By combining cutting-edge biometric sensing, AI-powered insights, and evidence-based behavioral coaching, Myant helps individuals and healthcare teams work together to prevent disease, optimize wellness, and unlock healthier, longer lives.

We are seeking a high-caliber Senior Product Quality Engineer to lead the quality lifecycle of our medical application and firmware. You will be the technical "glue" between our clinical users and our engineering team. This is not a standard "check-the-box" QA role; you will be responsible for investigating complex system failures, performing deep-dive firmware testing, and translating real-world clinical challenges into actionable engineering solutions.

Key Responsibilities:

1. Clinical Triage & Root Cause Analysis (40%)

• Act as the highest level of technical escalation for clinician-reported issues.
• Perform deep-dive forensic analysis on system logs, firmware behavior, and app performance to identify root causes.
• Conduct "Post-Market Surveillance" by identifying patterns in field failures and advocating for long-term technical debt resolution.

2. Deep-System QA & Validation (40%)

• Design and execute complex manual test suites that simulate real-world clinical environments (Hardware-in-the-loop).
• Validate firmware updates and software patches, ensuring zero regression in high-stakes medical environments.
• Develop "Edge Case" testing protocols based on observed clinician behaviors that automated tests might miss.

3. Process Leadership (20%)

• Establish a formal "Field-to-Engineering" feedback loop to ensure customer complaints directly inform the product roadmap.
• Assist in maintaining regulatory compliance (e.g., ISO 13485 or IEC 62304) by documenting anomalies and CAPA (Corrective and Preventive Actions) where necessary.
• Mentor junior engineers on the nuances of firmware/software integration.

Required Qualifications

• Experience: 5+ years in a technical QA, Systems Engineering, or Product Quality role, ideally involving both hardware and software.
• Domain: Experience in the Medical Device or Life Sciences industry is highly preferred (understanding the "criticality" of a system failure).
• Technical Depth:
  • Proficiency in reading logs and using debugging tools for embedded systems/firmware.
  • Experience with mobile/web app testing in a networked environment (clinics/hospitals).
• Soft Skills: Exceptional communication skills with the ability to remain calm and analytical when faced with "emergency" escalations from time-sensitive clinical environments.

Why This Role is Different

Unlike a traditional QA role, you have the autonomy to influence the product. You aren't just finding bugs; you are the primary advocate for the clinician’s experience. You will have the authority to "stop the line" if a release does not meet the stability standards our customers require.