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.

Assembly Technician – Clean Room

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

Magenta Medical, a fast-growing medical device startup, is expanding its manufacturing operations!

We are seeking motivated Assembly Technicians to join our production team and contribute to the development of life-saving medical technology

Responsibilities:

  • Perform device assembly for clinical use in a controlled clean room environment.
  • Work with a variety of production technologies and follow Magenta’s processes and work instructions.
  • Conduct fine assembly work under a microscope.
  • Handle and process chemical materials safely and according to procedures.
  • Clean and prepare components and equipment before entering the clean room.
  • Support cleaning and maintenance of the clean room.
  • Perform inspection and packaging activities throughout the production process


Reports to:

Production Director

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Design Assurance Engineer

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

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.

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.

Reports to:

QA Manager

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).

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Embedded Software Engineer

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

We are seeking an experienced Software Developer to join our SW/HW team and play a significant and central role in developing the software for the innovative Magenta System.  We are specifically looking for a candidate with strong systemlevel thinking and the ability to manage complex tasks and project timelines. This position combines Firmware development with a critical User Interface (UI), offering an exceptional opportunity for professional growth within a demanding medical High-Tech environment.

Key Responsibilities:  

  • Manage software versions and upgrades for existing products.
  • Design and develop all software aspects of the company’s products.
  • Oversee the entire software lifecycle, including development, testing, and documentation.
  • Manage external subcontractors for software development and validation.
  • Maintain a system-wide perspective and responsibility for all software components.
  • 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 firmware development, developing for sensors, brushless motors, and stepper motors.
  • Knowledge of communication protocols (e.g., UART, SPI, I2C) – must.
  • Software integration and development with the QT framework and QML.
  • 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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Information Systems Engineer \ Project Manger

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

We are seeking an Information Systems Engineer to support the establishment and continuous improvement of the company's Information Systems infrastructure.

As part of the Information Systems team, you will be responsible for developing, maintaining, and overseeing the day-to- day operations of the organization’s information systems, ensuring optimal functionality, data integrity, and user satisfaction. Provide support in system configuration, troubleshooting, documentation, and project execution under the guidance of senior team members.

The position involves supporting and managing cross-organizational projects in the field of information systems (ERP, MRP, QMS), while also providing daily user and system support across the company.

Responsibilities include:

  • Support all project phases, from planning and requirements definition through go-live.
  • Map, analyse, and optimize business processes.
  • Coordinate and monitor system implementation and development activities.
  • Write functional and operational specifications.
  • Prepare and execute validation protocols for electronic processes.
  • Support data optimization and migration between systems.

Reports to:

Information System Project Manager.

Education & Skills Requirements:

  • Bachelor’s degree in information systems, Industrial Engineering, or a related field.
  • 2-4 years of experience in information systems projects management, implementation, or project coordination.

Technical Skills:

  • Basic understanding of ERP/CRM systems.
  • Familiarity with databases and data analysis tools.
  • Knowledge of MS Office applications.
  • Strong problem-solving skills.
  • Good communication and interpersonal skills.
  • Ability to work collaboratively in a team.

Nice to have:

  • Basic understanding of medical device regulation and QMS systems.
  • Familiarity with the Priority ERP system.


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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.

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Purchasing Specialist

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

We are seeking a hands-on Purchasing Specialist to join our expanding Operations team.

This is a dynamic, end-to-end role that combines supplier management, full support for production and R&D, and responsibility for logistics and import/export processes.


  • Complete management and documentation of procurement and supply chain processes in the Priority ERP system – mandatory.
  • End-to-end purchasing of components, assemblies, and equipment for production (BOM) and R&D departments.
  • Responsibility for general purchasing – price quotations, purchase orders, shipment tracking, and goods receipt/inventory.
  • Handling import/export processes, working with customs brokers, and ensuring compliance with medical regulatory requirements (including AMAR approvals – a significant advantage).
  • Managing bottlenecks and coordinating with internal and external departments to ensure operational continuity.
  • Monitoring inventory, open orders, and supply planning.
  • Continuous improvement of procurement and logistics processes as part of company growth.

Reports to:

Sr. Director of Operations

  • 3+ years of procurement experience (medical device/pharma/biotech industry – an advantage).
  • Relevant academic degree in Logistics, Business Administration, Industrial Engineering & Management, or Supply Chain Management.
  • Strong understanding of development and production processes – start-up experience is an advantage.
  • Proven experience in global import/export processes, including working with customs brokers (AMAR approvals – significant advantage).
  • Familiarity with materials, components, and suppliers specific to the medical device industry.
  • Experience working with global suppliers, including China, Europe, and the USA.
  • Strong commercial and professional negotiation skills, with the ability to lead complex supplier processes.
  • Proficiency in ERP systems – mandatory.
  • High-level English – mandatory.
  • Ability to lead end-to-end processes in a dynamic start-up environment.
  • Proactive mindset, flexibility, and problem-solving skills in real time.
  • Excellent negotiation and interpersonal skills, with ability to collaborate across diverse teams.
  • Entrepreneurial approach, “Can-Do Attitude”, and motivation to be part of a small but impactful team.


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Research and Development Mechanical Engineer

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

We’re looking for a talented and hands-on Mechanical Engineer to join our growing R&D team. This is an exciting opportunity to play a key role in developing life-saving medical technology in a fast-paced and innovative startup environment.

• Participate in design and development activities for all aspects of the company’s products.

• Lead mechanical development tasks and sub-projects within the R&D team.

• 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

Reports to:

R&D Team Leader.

  • B.Sc. in Mechanical Engineering is required; candidates with degrees in Biomedical Engineering or Materials Engineering will also be considered.
  • M.Sc. in Mechanical Engineering – an advantage.
  • 3–5 years of hands-on experience in mechanical development roles – required.
  • Demonstrated experience working on complex, high-precision systems (e.g., medical devices, aerospace, robotics) – highly desirable.
  • Proven ability to take end-to-end ownership of mechanical components or sub-systems – from concept or design modifications to transfer to manufacturing.
  • Previous experience in startup environments – an advantage.
  • Strong hands-on lab skills and familiarity with mechanical testing – must.
  • Proficiency in CAD tools (SolidWorks preferred); knowledge of LabView and MATLAB – a plus.
  • Strong analytical thinking, problem-solving skills, and attention to detail.
  • Excellent written and verbal communication skills in English.


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Warehouse & Cleanroom Logistics Specialist

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

We are seeking a highly motivated and detail-oriented Warehouse & Cleanroom Logistics Specialist to join our Supply Chain team.

In this key role, you will be responsible for managing daily warehouse operations while ensuring that all preparation and logistics activities are executed in a controlled Cleanroom environment. Your responsibilities will include overseeing sterilization cycles and preparing production kits to support the Production Department

Responsibilities:

  • Manage daily warehouse activities, including goods receipt, inventory management, warehouse organization, work order preparation, equipment organization for clinical trials, and sterilization logistics.
  • Oversee goods receipt, ensuring accurate recording and handling of all incoming items.
  • Monitor inventory levels and notify relevant personnel when stock falls below the minimum threshold.
  • Prepare work orders and assembly kits for the production team, ensuring timely completion and adherence to required standards.
  • Warehouse Maintenance – ensure warehouses are consistently clean, organized, and well-maintained
  • Equipment organization for clinical trials, ensuring all the equipment is sterilized and is ready for use.
  • Manage sterilization logistics cycles to meet operational requirements





Reports to:

Supply Chain Manager.

  • 2–5 years of experience in warehouse and logistics operations, preferably from manufacturing companies in the medical device, biotech, or pharmaceutical industries – must.
  • Experience working in a Cleanroom environment – strong advantage.
  • Experience in logistics roles supporting production – advantage.
  • Previous experience as an assembly technician in a Cleanroom may also be suitable.
  • Experience with ERP systems (Priority – advantage).
  • Fluency in English – must.
  • Strong organizational skills, attention to detail, and ability to thrive in a fast-paced environment


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