QA Ops Platform Lead

Description:

Biosense Webster R&D Haifa Technology Center (HTC) is located in Yokneam, Israel. The HTC teams partner with leading physicians from around the globe to develop innovative MedTech solutions that improve the quality of care for patients worldwide.

The company's work is built on a proud legacy of leadership in electrophysiology. What began in the 1990’s with the founding of Biosense has evolved to present-day expertise driving best-in-class solutions in cardiac ablation, stroke care, intracardiac imaging and navigated ENT surgery.

Innovation is at the forefront at the Haifa Technology Center. HTC has been the top patent applicant in Israel for a decade. To fuel its innovation, experts in systems engineering, software integration, image integration, ultrasound capabilities, 3D printing and miniature sensors work collaboratively to create solutions that improve physician workflow and patient outcomes. HTC is also embracing the future of patient care by pioneering next-generation digital solutions, such as cloud-based applications that are powered by artificial intelligence.

A culture of continuous learning gives HTC employees fresh perspective to fuel continuous innovation and growth. The company embraces the unique perspectives, backgrounds and ideas of its employees, and provides them a fascinating career path and an opportunity to impact patients' lives.

We are looking for an experienced QA Ops Platform Lead

The QA Ops Platform Lead is responsible for end-to-end quality management per product families, Starting from Supplier selection and qualification, through design transfer activities and maintaining supplier and process control during the product lifecycle.

The QA Ops Platform Lead is mainly responsible for:

• Support activities related to testers development /update through production.
• Manage process validation, including supplier guidance.
• Review and approve supplier nonconformance, Investigations and lead improvement plans with the suppliers
• Operations Production stabilization, trend analysis and process improvements.
  
  

• BSc in Engineering or Practical Engineering with Qualification in Quality Assurance (CQE, CQM or CQA).
• Experience in medical systems or medical device companies – advantage.
• Demonstrated knowledge of manufacturing principles, practices, and procedures.
• Experience with validations (IQ/OQ/PQ/TMV) and supplier management
• Leading multidisciplinary project and processes
• Good communication skills, both verbal and written in English.