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 looking for a highly skilled and motivated Assistant Controller to join our finance team and support the company’s financial operations.
Reports to: Financial Controller
Responsibilities• Oversee payroll controllers in Israel and the US, as well as the overall payroll process.
• Support the bookkeeper and provide guidance on accounting matters.
• Ensure compliance with company policies and processes, including travel expenses and expense reimbursements.
• Assist in the preparation of quarterly and annual financial statements.
• Prepare the annual tax report and fulfill other statutory reporting requirements.
Qualifications
• CPA post-internship with a minimum of 2 years of experience as an assistant controller – must.
• Fluency in English (both spoken and written) – must.
• Strong proficiency in Excel and the ability to quickly learn new software and systems – must.
• Familiarity with Priority and QuickBooks – preferred.
• Excellent communication skills and a team-oriented mindset.
• Strong analytical abilities, detail-oriented.
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 to hire a Quality Assurance Assistant.
The assistant will implement and provide ongoing support for document control and other general QMS activities as necessary, in line with our unwavering commitment to quality.
Reports to: QA Manager
ResponsibilitiesDocument Control Activities:
• Operation and maintenance of the eQMS (Electronic Quality Management System) – Dot Compliance.
• Implementation and ongoing support of all Document Control activities.
• Process Document and Engineering Change Orders (DCO and ECO).
• Support and maintain all company Device History Files (DHF) and Device Master Record (DMR).
Qualifications
• Bachelor’s degree in a relevant field.
• At least 3 years of experience in a similar or relevant role.
• Excellent written and verbal communication skills.
• Ability to manage time effectively to ensure timely completion of tasks.
• Proficiency in PC usage, including Microsoft Word, Excel, PowerPoint, and other Office applications.
• Capability to work independently and collaboratively in a cross-functional team environment.
• Highly detail oriented.
• Fluency in English, both written and spoken.
We are seeking to hire a Quality Design Assurance Engineer to join our QA team.
As a Design Assurance Engineer, you will lead all quality elements of Design Controls and product DHF for new product introductions and sustaining/design projects.
Reports to: QA Manager
Responsibilities• Quality responsibility to verify that the design and development process follows the procedures and design and development plans.
• Work closely with R&D and test teams to support regulatory requirements by creating, reviewing, and providing quality and compliance input to the design and development process, deliverables, and requirements.
• Participation in project meetings to review and help update clear and concise user requirements, product specifications, plans, verification and validation studies, risk management files, and other relevant design control deliverables.
• Quality responsibility for transferring new products and sustaining projects to manufacturing and operations quality and supplier quality teams.
• Support the Regulatory Affairs department for submissions and respond to submission questions, implementation of new or revised standards and support internal and external audits.
Qualifications
• At least 2-3 years of experience working in a quality function in the medical device industry – must.
• At least 1 year of experience as a design control engineer (preferred).
• A Bachelor of Science in Engineering, Sciences, or a related field – must.
• Familiar with statistical techniques used in verification and validation processes – must.
• Experience with ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards – must.
• Strong analytical and problem-solving skills, with keen attention to detail.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.
• Proficient use of standard MS Office applications.
• Fluent in English (oral and written).
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!