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.

Embedded Software Engineer

Magenta Medical - IL, Full-time, On-site

About the Role - 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

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

Reports to:

Sr. Director of SW and HW Development

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

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Financial Controller

Magenta Medical - IL, Full-time, On-site

About the Job

We are looking for a highly skilled and motivated Financial Controller to join our finance team and support the company’s financial operations.

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.

Reports to:

Financial Controller

• 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

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Mechanical Engineer (NPI)

Magenta Medical - IL, , On-site

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.

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.

Reports to:

Director of Engineering

B.Sc. in Mechanical Engineering - must.

3-5 years of experience in the medical device industry - must

Proficiency in SolidWorks and PDM - must.

Strong analytical skills.

Excellent written and verbal communication skills

The form has been successfully submitted!

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Regulatory Affairs Associate

Magenta Medical - IL, Full-time, On-site

We are seeking an experienced Regulatory Affairs Associate to join our team.

The Regulatory Affairs Associate will support Magenta’s products from early feasibility through marketing authorization, ensuring compliance with regulatory requirements. This role will work closely with other departments to maintain regulatory adherence and facilitate successful product approvals

Provide regulatory support for Magenta’s products from early feasibility through marketing authorization.
Prepare and maintain regulatory submissions and registrations for Magenta’s products in relevant markets.
Conduct technical reviews of data and reports for regulatory submissions to ensure accuracy and clarity.
Assess changes to device design or processes to determine their impact on pending or existing registrations.
Provide guidance to project teams on premarket regulatory requirements, labeling standards, and other compliance matters.
Monitor and communicate updates on new or revised guidance, regulations, and industry initiatives to ensure regulatory compliance.

Reports to:

Vice President, Regulatory Affairs & Quality Assurance

Bachelor’s degree in a scientific, technical, or engineering discipline – must.
Minimum of five years of Regulatory Affairs experience with the US FDA and EU regulatory agencies (Class II and/or Class III medical devices) – must.
Alternatively, candidates with a strong background in Design Quality Assurance seeking to specialize in Regulatory Affairs will be considered.
Excellent writing and editing skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.
Proficiency in standard MS Office applications.
Fluency in English, both oral and written

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Technician

Magenta Medical - IL, Full-time, On-site

We are expanding our manufacturing operations and recruiting assembly technicians for our production team.

Our unique manufacturing process is conducted in a controlled environment using a variety of production technologies

Responsibilities:

Manufacturing Activities Device assembly for clinical use in the controlled environment area (clean room).
process for Magenta’s products and per Magenta’s procedures and Work Instructions including the handelling of chemical materials.
Cleaning components and equipment before entering the controlled environment area (clean room)
Cleaning and maintenance of Clean Room.
Fine assembly work under a microscope.
Perform all required manufacturing, inspection and packaging activities along the production.

Reports to:

Production Director

Experience working in a Controlled Environment Area (Clean room).
Understanding of assembly instructions and drawings.
Previous experience in a medical device company or the healthcare field is an advantage.
Attention to details.
A team worker, well orgenized.

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