Careers

Who are we?

At MeMed, our mission is to translate the immune system’s complex signals into simple insights that transform how diseases are diagnosed and treated, profoundly benefiting patients and society. Our FDA-cleared technology is already in use, and we are now rapidly scaling globally, offering a unique opportunity to join us at a pivotal stage and help impact the lives of millions of patients worldwide.

The Role

We are seeking a strong Systems Engineer to join our R&D team in Haifa. This role is responsible for system-level architecture definition, requirements, interface definition, and risk management for a multidisciplinary IVD platform integrating hardware, software, and biological/chemical components. The Systems Engineer role includes cross-functional technical leadership and close collaboration with internal teams and external partners. The position reports to the Director of Systems Engineering.

Key Responsibilities

• Lead system-level requirements activities throughout the product lifecycle, including definition, decomposition, traceability, and change impact assessment.
• Own and maintain the risk management file and associated deliverables in accordance with ISO 14971.
• Develop and support system integration plans in collaboration with internal teams and external partners.
• Provide technical leadership for cross-disciplinary initiatives, including requirements definition, interface alignment, review of design outputs, and verification readiness.
• Support investigations of system issues and field complaints, including data analysis, root cause identification, and hands-on laboratory or technical work as required.
• Participate in defect management and resolution processes.
• Lead and participate in design reviews and design control activities
• Support audits and regulatory documentation as needed.
• Serve as the technical focal point for global third-party engineering partners
• Collaborate closely with R&D, QA/RA, Product Management, Operations, and external vendors to ensure timely, high-quality delivery.

Required Qualifications

• B.Sc. in one of the following fields: Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Computer Science, Physics, or a related discipline.
• 2–5 years of experience in systems engineering in multidisciplinary development environments.
• Experience in medical devices or regulated product development; IVD experience is an advantage.
• Demonstrated experience performing risk management activities in accordance with ISO 14971.
• Experience working with and coordinating external engineering partners in regulated development environments
• Strong analytical and problem-solving skills, including structured investigation and root cause analysis.
• Clear written and verbal communication skills in English; ability to work effectively across functions.

Preferred Qualifications

• M.Sc./M.E. in an engineering or science discipline.  
• Experience working with external development partners, subcontractors, or suppliers.
• Experience with point-of-care diagnostics systems.
• Experience integrating chemistry or biology within engineering systems.
• Proficiency in scripting for data analysis and automation (e.g., Python).
• Familiarity with statistical analysis techniques for verification and investigations.
• Familiarity with relevant standards and regulations (e.g. FDA, IVDR, IEC 61010, IEC 60601)

Key Competencies

• Strong ownership mindset and attention to detail.
• Systems thinking mindset.
• Self-directed, able to manage multiple priorities.
• Ability to drive alignment and execution across functions without direct authority.