Quality Engineer
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The role in plain words
- Minimum 5 years of experience as a Quality Engineer in a medical device company or other regulated industry
- Ability to read drawings and understand technical requirements
- Strong organizational skills and good cross-functional communication abilities
- Proficient in written and verbal English
- Auditor certification
- Experience in a small or growing organization
Extracted from the job description · kept up to date automatically
Who this suits
Full job description
Original listing · kept for referencePosition Overview
Lifeward is a global leader in advanced rehabilitation and mobility technologies, pioneering solutions that restore function and independence for individuals with neurological and physical impairments. The company’s portfolio includes powered exoskeleton systems, anti-gravity rehabilitation platforms, and next-generation wearable and AI-driven technologies, serving both clinical and home-use environments.
Building on a strong foundation of innovation and clinical impact, Lifeward is expanding its product portfolio and scaling operations through global manufacturing partnerships. The company is focused on delivering high-quality, reliable products while accelerating the development of next-generation systems and entering new therapeutic and assistive applications.
The Quality Engineer will play a key role in supporting production and supplier quality activities, ensuring robust, compliant, and scalable processes that enable continued growth and product excellence.
Primary Responsibilities:
• Support production quality activities, including: Final QC, Device History Record (DHR) review and management, incoming inspection, handling of nonconforming materials
• Support supplier quality activities, including: Supplier qualification and monitoring, supplier corrective actions
• Manage and support: Calibration activities, employee qualification and training records
• Work closely with Operations, Quality, and R&D teams on: Ongoing production support, process improvements, daily quality-related activities
• Support change control activities to ensure controlled implementation of changes
• Contribute to maintaining fluent, compliant, and controlled processes across production and supply chain
Experience / Skill Requirements:
• Minimum 5 years of experience as a Quality Engineer in a medical device company or other regulated industry
• Familiarity with medical device quality standards and processes
• Ability to read drawings and understand technical requirements
• Strong organizational skills
• Good cross-functional communication abilities
• High level of personal accountability
• Auditor certification – advantage
Other Requirements:
• Highly reliable and detail-oriented
• Ability to work under pressure and prioritize tasks
• Ability to work effectively in a global team environment
• Experience in a small or growing organization – advantage
• Proficient in written and verbal English
Reporting to: Quality/Regulatory Director
Location: Yokneam, Israel
Questions about this role
- This listing did not state a salary. We only show pay when the employer publishes it.
- Minimum 5 years of experience as a Quality Engineer in a medical device company or other regulated industry, Ability to read drawings and understand technical requirements, Strong organizational skills and good cross-functional communication abilities, Proficient in written and verbal English