Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

CathWorks, recently acquired by Medtronic, is the leader in digital health innovations that improve the lives of patients globally. The CathWorks FFRangio® System combines AI and computational science to obtain physiologic information from routine angiograms (X-rays), eliminating the need for drug stimulation and invasive pressure wires. It provides physicians with a quick and reliable intraprocedural physiologic assessment for the entire coronary tree, making it practical for every patient.

As a Quality Engineer based in Kfar Saba, you will play a key role in supporting day-to-day quality activities while helping harmonize quality and regulatory processes across the organization. This position focuses on design controls, CAPA, complaint handling, software development lifecycle activities, and regulatory compliance within a regulated medical device environment. You will collaborate with cross-functional teams to ensure quality system requirements are effectively implemented, maintained, and continuously improved, supporting the delivery of innovative technologies that advance patient care.

• Assist in aligning and implementing design control processes, including requirements management, design reviews, verification/validation, and traceability.
• Support the mapping, migration, and harmonization of quality system processes, including document control, training, audits, and related quality activities; support internal and external audits as applicable.
• Participate in the integration and standardization of CAPA and complaints handling processes, ensuring effective root cause analysis, corrective and preventive actions.
• Support software development lifecycle processes, including requirements management, design reviews, validation, and testing.
• Ensure all integrated processes meet applicable regulatory requirements (FDA, MDR, ISO 13485, 21 CFR Part 11, etc.), including electronic records and signatures, risk analysis, and audit readiness.
• Assist in updating and maintaining quality documentation, provide training to stakeholders on new or revised processes, identify process gaps, and support continuous improvement initiatives.

Required Knowledge and Experience:

• Bachelor’s degree in Engineering, Life Sciences, or a related field.
• 3+ years of experience in medical device quality engineering, including QMS, design controls, CAPA, complaints management, and software validation.
• Working knowledge of FDA regulations, MDR, ISO 13485, and 21 CFR Part 11 requirements.
• Experience with software development lifecycle processes in regulated environments is an advantage.
• Strong analytical, communication, and teamwork skills, with the ability to work effectively in cross-functional environments.

Experience with QMS integration or harmonization projects and electronic QMS platforms would be considered an advantage.

Physical Job Requirements

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Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. 

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If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected].

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Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).