Come Work With Us!
Magenta Medical is a medical device company developing the world’s smallest heart pump, meant to provide minimally-invasive support to the heart during acute episodes of dysfunction. The Elevate™ System is multi-disciplinary, involving mechanical engineering, material science, electrical engineering, software, algorithms, and state-of-the-art catheter fabrication techniques.
We are seeking exceptional individuals to help drive the Elevate™ System forward and potentially save more lives.
We are seeking a talented Clinical Specialist to join our Clinical team.
Reports To: Senior Manager, Clinical Specialist team.
Responsibilities
• Coordinate and provide case support to the physicians in clinical trial procedures in compliance with Good Clinical Practice (GCP), regulatory guidelines, and protocols.
• Responsible for training the clinical site personnel and investigators on the proper use of the Elevate System via education sessions and case support.
• Monitoring trial progress and ensuring compliance with regulations.
• Liaising with the clinical sites and Clinical Trial Management (CTM) team to enhance the clinical trial process.
• Logistics coordination for cases, clinical trial device inventory.
• Ability to travel up to 80% within the region required.
Qualifications
• A bachelor’s degree in life sciences, nursing, or a related field – must.
• Familiarity with clinical trial phases and processes – must
• Experience in interventional cardiology and invasive cardiac therapies – must.
• Vast knowledge of hemodynamic monitoring and support – must.
• Experience with Mechanical Circulatory Support (MCS) – must.
• Ability to adapt appropriately in stressful situations.
• Excellent organizational and intrapersonal skills.
• Strong execution and ability to work collaboratively in a cross-functional team environment.
• Advanced self-learning and problem-solving abilities.
• Capable of identifying and addressing operational challenges proactively.
We are seeking a Software Developer who will have the opportunity to grow and learn while playing a key role in developing software for the innovative Magenta System.
Reports to: Sr. Director of SW and HW Development
Responsibilities
• Design and develop all software aspects of the company’s products.
• Manage software versions and upgrades for existing products.
• Oversee the entire software lifecycle, including development, testing, and documentation.
• Manage external sub-contractors for software development and validation.
• Maintain a system-wide perspective and responsibility for all software components.
• Design, implement, and integrate firmware and user interface (UI).
• Manage software lifecycle development, generate software requirements and specifications, and create all relevant software lifecycle deliverables.
• Conduct design reviews in accordance with company policies.
• Provide input on software usability.
Qualifications- B.Sc. or higher in Computer Science or another Engineering degree – must.
• 3+ years of experience in SW software development – must.
• Proficiency in mixed C/C++ programming – must.
• Proven experience with STM32 microcontroller firmware development, developing for sensors, brushless motors, and stepper motors – must.
• Knowledge of communication protocols (e.g., UART, SPI, I2C) – must.
• Software integration and development with the QT framework and QML – must.
• Knowledge of AWS and Docker architecture, Python, and React – advantageous.
• Experience in the medical device industry – advantageous.
• Strong problem-solving skills & interpersonal skills.
• Excellent written and verbal communication skills.
We are looking for a highly motivated engineer with experience in both software validation and lab work to join our dedicated team.
Reports To: Project Manager
Responsibilities
• Participate in testing activities of the mechanical and clinical aspects of the company’s products, with a focus on V&V bench tests of products and R&D prototypes.
• Conduct and coordinate product testing under defined conditions to verify or reject product specifications using scientific methodologies.
• Perform product testing on components and systems during the R&D phase.
• Develop test methods to support the testing process throughout prototype development and assembly.
• Write protocols and reports detailing testing procedures and results.
• Support animal studies and experiments, including handling biological tissues and blood samples.
Qualifications
• B.Sc. in Biomedical, Biotechnology, Electrical, and Electronics or another engineering degree – must.
• Hands-on laboratory experience – must.
• Software testing experience – an advantage.
• Understanding of test protocols – an advantage.
• Experience in data analysis – an advantage.
• Experience with CAD software, especially SolidWorks – an advantage.
• Strong ability to follow written and verbal instructions in both English and Hebrew.
• Precise data collection, recording, and reporting capabilities.
• Strong attention to detail.
Don’t see the position you’re looking for? We would still love to hear from you!