Come Work With Us!
Magenta 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 looking for the best people possible who can help us propel the Elevate™ System forward and save more lives.
We are looking for a talented Mechanical Engineer to join our Engineering team and take the lead on multiple processes and a complex product – making the transfer to manufacturability.
Reports to: Director of Engineering
Responsibilities
Design and lead NPI processes such as:
• Collaborate and share data with R&D, Production, and Quality in integrating and implementing process modification.
• Early engagement with R&D activities and support design updates to be serial-production-worthy documentation.
• Design verification tests- process and fixtures
• Support production with process-based challenges
• Design fixtures and jigs to improve manufacturing processes.
• Lead ECO process and support conformity reports.
• Full control of in-scop product’s BOM, DMR, and documentation.
Qualifications
• B.Sc in Mechanical Engineering-must.
• Recommended three years of experience in the medical device industry.
• Proficiency in Solid works (and PDM).
• Analytical skills.
• Good written/verbal communication skills.
We are currently seeking a pre-clinical associate who will participate in in-vivo studies performed with the Company’s products, both locally and abroad (work-related travel up to 50% abroad).
Reports to: Sr. Director of Pre-Clinical
Responsibilities
• Perform and monitor animal studies for both R&D and pre-submission/submission activities.
• Document and report online information during studies.
• Maintain accurate records of all testing data and results in the specified forms (paper and electronic) in accordance with the company’s guidelines.
• Handle biological tissues and blood samples.
• Provide general assistance in pre-clinical assignments.
Qualifications
• BSc or MSc in Biology, Biomedical Engineering, Veterinary Medicine, or a related field – must.
• Ability to travel periodically for 1-2 weeks at a time – must.
• Ability to work nights periodically for 1-2 weeks at a time – must.
• Two years of experience with pre-clinical studies – advantage.
• Dedication and proactiveness, with the ability to complete tasks in urgent and stressful situations.
• Highly creative, adaptive, and flexible thinker.
• Excellent proficiency in English (oral and written).
• Strong ability to handle complex situations.
We are looking for a dynamic and experienced Project Manager who will be part of the PMO team.
Reports to: Engineering & Project Manager
Responsibilities
Assist with project planning, coordination, and execution:
• Set a timeline and monitor project deliverables.
• Update relevant stakeholders or team members on the project’s progress.
• Coach and support project team members with tasks you assign them.
• Develop detailed project plans, define scope and objectives, and coordinate activities to ensure successful execution within established timelines.
• Integration of multidisciplinary systems, including mechanics, materials, electronics, and software.
• Collaborate with multidisciplinary teams, including R&D, engineering, QA/R ,clinical, and manufacturing.
• Identification of bottlenecks in existing work processes and definition of appropriate solutions in collaboration with the professional team
Qualifications
• B.Sc. Engineer in mechanical/ biomedical/ materials science (or other relevant degree).
• 4+ years of experience in a similar role in a medical device company – must.
• Experience with the entire product lifecycle, from early development stages to complete transfer for production must.
• High hands-on technical skills and experience in CAD (SolidWorks – Model & Drawings) are advantages.
• Excellent communication and interpersonal skills.
• Ability to lead and motivate cross-functional teams.
• Excellent writing and verbal skills with solid proficiency in English and Hebrew.
• Ability to thrive in a fast-paced and dynamic work environment.
We are looking for an experienced mechanical Engineer who will be joining our R&D Group.
Reports to: R&D Team Leader
Responsibilities
• Participate in design and development activities for all aspects of the company’s products.
• Design mechanical parts and assemblies’ issue 2D drawings.
• Generate test methods and design fixtures to support the test during the development and assembly of prototypes.
• Conduct feasibility research.
• Interact with suppliers and manufacture R&D prototypes.
• Conducted test jigs qualifications and performed engineering verification and validation tests.
• Provide technical usability engineering input.
• Develop a mechanical User Interface.
• Provide technical engineering input for risk management activities.
• Perform the role of a Field Clinical Engineer (FCE).
Qualifications
• B.Sc in Mechanical Engineering- must.
• Master’s degree in mechanical engineering – an advantage.
• 1-3 years experience in the medical device industry.
• Hands-on experience in the laboratory- must.
• Experience with CAD software, Solidworks, LabView, and MatLab knowledge is preferred.
• Analytical skills.
• Good written/verbal communication skills.
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.
Don’t see the position you’re looking for? We would still love to hear from you!