Quality Engineering Specialist; On SIte

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.

Myant is a leading innovator in textile‑based technology, leveraging advanced materials, smart fabrics, wearable technology and software platforms to transform how people monitor and manage their health and wellness. As Myant continues to scale its medical device manufacturing and expand across North American and European markets, we are seeking a Quality Engineering Specialist to strengthen manufacturing processes, supplier quality and quality systems within a regulated medical device environment.

• Manufacturing Quality & Process Control
• Review, investigate and support the disposition of non‑conforming materials, components and devices identified through incoming inspection or active production
• Support quarantine, containment and disposition activities in accordance with established procedures and QMS requirements
• Lead or support root cause analysis and Corrective and Preventive Action (CAPA) investigations related to recurring assembly, material or manufacturing defects
• Develop, implement and maintain appropriate inspection criteria, sampling plans and acceptance criteria for incoming materials, work‑in‑process and finished products
• Apply appropriate statistical sampling methodologies, including ANSI/ASQ Z1.4, where applicable
• Develop and maintain specialized inspection and testing methods for raw materials, components and finished goods
• Monitor manufacturing data, process capability, yields and quality metrics to identify adverse trends before they result in product failures, increased scrap or batch rejection
• Support the implementation of Statistical Process Control (SPC) and other data‑driven process control methodologies
• Partner with Manufacturing and Operations teams to identify opportunities to improve process capability, yield, reliability and consistency
• Provide technical quality support for manufacturing issues and process improvements
• Validation, Verification & Risk Management
• Review, oversee and approve validation protocols and reports for manufacturing equipment, processes, assembly lines and applicable software systems
• Support and/or lead Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) activities
• Develop and maintain quality engineering documentation supporting manufacturing validation and process changes
• Lead and facilitate cross‑functional…