Quality Assurance Engineer
פורסם אתמול · 37 מועמדים
- BSc in Engineering
- 2+ years of experience in quality assurance, engineering, or a related role
- Experience with design controls, DHF, DMR, ECO/configuration management, and document control
- Strong organizational skills and attention to detail
- High ownership and ability to work effectively across multidisciplinary teams
- Quality management system (QMS) experience
חולץ מתיאור המשרה · מתעדכן אוטומטית
תיאור המשרה המלא
המשרה המקורית · נשמר לעיוןAbout the Role:
Discure Technologies is seeking a highly motivated, hands-on QA Engineer to join our team as we advance our implantable bioelectronic device toward a pivotal clinical study. This is a full-time, office-based position in Petah Tikva, BSR City, reporting to the QA Manager. The QA Engineer will implement and manage the quality system in a multidisciplinary development environment, with ownership of design controls, configuration and document control, quality records, suppliers, and equipment documentation. In addition to core quality responsibilities, the role will include hands-on involvement in selected engineering, product development, and manufacturing activities.
The role requires close collaboration with R&D, regulatory, manufacturing, and external partners.
Key Responsibilities
· Help implement and maintain the quality system within a multidisciplinary R&D environment
· Maintain the Design History File (DHF), ensuring complete, controlled, and traceable design records
· Manage product configuration, Device Master Records (DMR), Engineering Change Orders (ECOs), and manufacturing documentation
· Support select product development and manufacturing engineering activities, working closely with R&D and operations on design implementation, testing, and production-related tasks
· Manage document control for procedures, specifications, forms, and related documentation
· Manage quality records and ensure appropriate retention, traceability, and accessibility
· Maintain the Approved Supplier List (ASL) and related supplier quality documentation
· Maintain equipment logs and associated calibration and maintenance records
· Collaborate with R&D, regulatory, manufacturing, and suppliers to integrate quality requirements into development activities and support the transition of designs into controlled manufacturing
Qualifications and Requirements
· BSc in Engineering
· 2+ years of experience in quality assurance, engineering, or a related role in a regulated medical device development environment
· Experience with design controls, DHF, DMR, ECO/configuration management, and document control
· Strong organizational skills and attention to detail
· High ownership and ability to work effectively across multidisciplinary teams
· Medical device and quality management system experience - advantage
About Discure Technologies
Discure Technologies is a clinical-stage medical device company developing a minimally invasive, bioelectronic implantable device for degenerative disc disease. The Discure System is designed to reduce pain, restore function, and modify the disease process, with the goal of reducing the need for opioids and invasive back surgery. The company has received FDA Breakthrough Device Designation and was named “Best New Technology in Spine Care” by the North American Spine Society. Discure is backed by leading medtech, venture, and strategic investors, including Johnson & Johnson, BOLD Capital, Supernova Invest, and Sanara Capital.
שאלות על המשרה
- המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.
- BSc in Engineering, 2+ years of experience in quality assurance, engineering, or a related role, Experience with design controls, DHF, DMR, ECO/configuration management, and document control, Strong organizational skills and attention to detail, High ownership and ability to work effectively across multidisciplinary teams