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Director of Quality Assurance

RA/QA | Tel Aviv-Yafo, IL

About the position is the first company to successfully turn the smartphone camera into a clinical-grade medical device, enabling faster treatment and improved care for patients worldwide. Our products combine computer vision and machine learning technology with best-in-class UX design to create new clinical pathways through smartphone-powered urinalysis, digitized wound management, and beyond.

Headquartered in Tel Aviv with 240 employees across London, Boston, and Singapore we are growing fast as we serve more and more patients across ever-expanding areas of healthcare.

The Director of Quality Assurance (QA) will be responsible for leading's Quality Management System (QMS) activities that comply with EN ISO 13485:2016 standard, FDA QSR regulations, and other applicable standards for the assurance of the quality of company products.

  • 5-8 years of QA management experience in medical device companies; experience in software-based medical device companies is an advantage. 
  • Previous experience with FDA QSR regulations; past experience commercializing products in the US and FDA inspections is a plus.
  • Experience in quality systems complying with EN ISO 13485:2016 standard and the MDR, IVDR European regulations. 
  • An academic degree in exact sciences such as chemistry or biology is an advantage. 
  • Attention to detail and ability to manage multiple tasks. 
  • Ability to lead and manage independently. 
  • Full professional fluency in English. 
Role & Responsibilities

Managing and supporting company processes, with an emphasis on:

  • Management Review
  • Corrective and Preventive Actions (CAPAs)
  • Non-conforming products
  • Internal auditing 
  • Design Control and Software Development Life-Cycle (SDLC) and the creation and maintenance of products’ Design History Files (DHFs)
  • Creation and maintenance of Device Master Records (DMRs) and Device History Records (DHRs) 
  • Engineering Changes (ECOs)
  • Handling complaints
  • Employee’ Qualifications
  • Supplier and subcontractor evaluations according to the EN ISO 13485:2016 standard, FDA QSR regulations, and other applicable standards 

or send your CV to [email protected]