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


thank you

The form has been successfully submitted!

We’ll get back to you soon.

Read more

Mechanical Engineer

Magenta Medical - IL, , On-site

Magenta Medical is a Class III medical device company that develops the smallest and most powerful heart pump in the world. With commercial manufacturing and scale-up on the horizon, we're expanding our Operations and Engineering teams - join us to help build the foundation for success!

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 transition 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.

• Provide production support by addressing process-related challenges.

• Design fixtures and jigs to improve manufacturing processes.

• Lead ECO process and support conformity reports.

• Full control of the in-scope product’s BOM, DMR, and documentation.



Reports to:

Director of Engineering

• B.Sc. in Mechanical Engineering - must.

• 1-3 years of experience in the medical device industry.

• Proficiency in SolidWorks (and PDM).

• Analytical skills.

• Good written/verbal communication skills.


Why join now?

  • Be part of a startup atmosphere with the ambition for a commercial launch.
  • Play a pivotal role in building our manufacturing systems and processes from the ground up.
  • Work in a cross-functional team that values innovation, ownership, and impact.

thank you

The form has been successfully submitted!

We’ll get back to you soon.

Read more

Quality Assurance Engineer

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

We are looking for an Experienced Quality Assurance Specialist to join our QA Operations group and support the variety of activities related to QA Operations, such as:

  • Lead QA Operations activities with regards to verifications/validations for an FDA reviewed complex, multidisciplinary, active investigational device.
  • Lead and perform the Engineering Change Order (ECO) process from risk analysis through protocol approval.
  • Verification, execution, and analysis of reposts until FDA-ready.
  • Provide guidance to the R&D and Engineering teams on IQ/OQ/PV activities.

Reports to:

QA Manager


  • B.A. or B.S. degree in a technical discipline, such as Engineering or Science. 
  • 3-5  years of relevant experience in the medical device industry.
  • Previous experience with medical device verification/validations, ECOs, medical device statistics
  • Working knowledge of medical device international standards.
  • Ability to work independently with minimal work direction and in a cross-functional team environment.
  • Fluent in English with excellent writing skills, effective written and verbal communication skills. 
  • Excellent computer skills, including a working knowledge of Microsoft Office applications.
  • Strong time management abilities to ensure timely task completion. 
  • Detail-oriented.

thank you

The form has been successfully submitted!

We’ll get back to you soon.

Read more

Research and Development Mechanical Engineer

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

Magenta Medical is seeking a motivated Intermediate Research Development Mechanical Engineer to join our innovative team. The successful candidate will play a key role in the design and development of cutting-edge medical devices. You will collaborate with cross-functional teams to drive product development from concept through to production, ensuring compliance with regulatory standards and company objectives.
Responsibilities:

  • Design, develop, and prototype mechanical components and systems for medical devices.
  • Conduct experiments and tests to validate designs and improve performance, ensuring products meet quality and regulatory standards.
  • Collaborate with electrical engineers, software developers, and regulatory teams to create innovative solutions.
  • Prepare technical documentation, including design specifications, test plans, and reports.
  • Participate in design reviews and provide constructive feedback to team members.
  • Assist in troubleshooting and resolving engineering issues during product development and manufacturing.

Reports to:

R&D Team Leader.

  • Bachelor’s degree in Mechanical Engineering or a related field.
  • A minimum of 3 years of experience in mechanical design and development, preferably in the medical device industry.
  • Proficiency in CAD software (e.g., SolidWorks, AutoCAD) and simulation tools.
  • Strong understanding of material properties and manufacturing processes.
  • Familiarity with regulatory requirements for medical devices (e.g., ISO 13485, FDA guidelines).
  • Excellent problem-solving skills and the ability to work collaboratively in a team environment.

thank you

The form has been successfully submitted!

We’ll get back to you soon.

Read more

Strategic Sourcing Manager

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

We are seeking a highly skilled and motivated Strategic Sourcing Manager to lead sourcing and procurement activities for medical device components, with a focus on identifying and managing suppliers in the United States.

In this role, you will be responsible for strategic sourcing initiatives, supplier relationship management, and cross-functional collaboration to ensure optimal supply performance in compliance with regulatory and operational standards.

  • Develop and implement sourcing strategies for key medical device components, including catheter systems, nitinol subassemblies, and electromechanical modules.
  • Identification, qualification, and evaluation of potential suppliers according to regulatory and operational requirements (FDA, ISO 13485, etc.).
  • Partner with Engineering teams to translate technical specifications into supplier-ready requirements.
  • Manage supplier selection, negotiations, onboarding, and performance monitoring across the U.S. and other key markets.
  • Build strong, long-term relationships with strategic suppliers to ensure continuity, quality, and scalability.
  • Collaborate with R&D, Quality, Regulatory, and Operations teams to align sourcing strategies with product and business needs.
  • Lead cost reduction and value engineering initiatives.
  • Stay ahead of industry trends and leverage supplier capabilities to support innovation.

Reports to:

Sr. Supply Chain Manager

  • Bachelor's degree in Engineering, Industrial Management, Logistics, or a related field.
  • 5+ years in strategic sourcing or procurement within the medical device industry (Class II/III preferred) or Life Sinece industiry.
  • Proven experience sourcing complex components (e.g., catheters, nitinol, PCBs, microelectronics).
  • Strong understanding of regulatory compliance (ISO 13485, FDA , supplier audits).
  • High proficiency in English (spoken and written).
  • Hands-on experience with ERP systems and supplier management tools.
  • A proactive, detail-oriented mindset with excellent interpersonal and negotiation skills.
  • Ability to thrive in a fast-paced startup environment with cross-functional responsibilities.



thank you

The form has been successfully submitted!

We’ll get back to you soon.

Read more

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.

thank you

The form has been successfully submitted!

We’ll get back to you soon.

Read more

Don’t see the position you’re looking for?

We would still love to hear from you!