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.

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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Materials Project Engineer

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

Magenta Medical is a Class III medical device company developing the world’s smallest and most powerful heart pump. As part of our commercial manufacturing and scale-up strategy, we are expanding our Engineering teams. Join us to help build the foundation for success!

We are seeking a talented Biomedical / Materials Engineer to join our Engineering team and take ownership of material and coating-related processes, driving a complex product through the transition from development to scalable manufacturing.

Responsibilities

  • Lead material and coating-related activities within New Product Introduction (NPI), including transfer from R&D to manufacturing.
  • Optimize manufacturing processes, including material-related processes, and support the design and development of production equipment, fixtures, and jigs.
  • Prepare and maintain manufacturing documentation (e.g., work instructions, SOPs, BOMs).
  • Provide hands-on production floor support through effective troubleshooting, root cause analysis, and corrective actions.
  • Collaborate with external suppliers and subcontractors to ensure quality, efficiency, and regulatory compliance.
  • Lead equipment and process qualification activities (IQ/OQ/PQ).
  • Lead engineering change orders (ECOs) and drive implementation to improve design and manufacturing outcomes.
  • Write test protocols and generate technical reports to support verification and validation activities.

Reports to:

Director of Engineering

  • B.Sc. in Biomedical Engineering or Materials Engineering (Mechanical Engineering background/orientation is an advantage).
  • 2–5 years of experience, preferably in the medical device industry (advantage).
  • Familiarity with quality assurance and regulatory standards (e.g., ISO 13485, GMP – if relevant).
  • Proven hands-on experience in process development and optimization.
  • Proficiency in SolidWorks (advantage).
  • Strong analytical and problem-solving skills.
  • Strong interpersonal skills and the ability to collaborate effectively across multidisciplinary teams.


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Project Manager

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

Magenta Medical is a Class III medical device company developing the world’s smallest and most powerful heart pump. As we continue to scale toward commercial manufacturing, we are seeking an experienced and driven Project Manager to join our team.

As a key team member, you will play a central role in leading and coordinating cross-functional development projects, from early-stage R&D through full production transfer. This position requires strong technical understanding, project management capabilities, and the ability to integrate multidisciplinary efforts into a cohesive execution plan.


Reports to:

CTO and General Manager

  • Lead project planning, coordination, and execution across all development stages.
  • Define project scope, objectives, timelines, and deliverables.
  • Monitor progress and ensure alignment with project milestones and company goals.
  • Provide regular updates to stakeholders and senior management.
  • Support and guide team members to ensure successful task completion.
  • Coordinate and integrate multidisciplinary systems (mechanics, materials, electronics, software)
  • Collaborate closely with cross-functional teams, including R&D, Engineering, QA/RA, Clinical, and Manufacturing.
  • Identify bottlenecks and inefficiencies in processes and drive continuous improvement initiatives.
  • Ensure smooth transfer from development to production (NPI process).


Qualifications:

  • B.Sc. in Mechanical Engineering, Biomedical Engineering, Materials Science, or a related field.
  • 4+ years of experience in a similar role in a medical device company - must.
  • Proven Experience with full product lifecycle, from early development stages to full transfer for production - must.
  • High hands-on technical skills, and experience in CAD (SolidWorks - Model & Drawings) - an advantage.
  • 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.
  • High hands-on technical skills.
  • Fluent in Hebrew and English (written and verbal)

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Senior 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. As a commercial manufacturing and scale-up approach, we're expanding our Operations and Engineering teams. Join us to help build the foundation for success!We are seeking a talented Mechanical/Biomedical/Material Engineer to join our Engineering team, leading multiple processes and a complex product through the transition to manufacturability.


Responsibilities

  • Lead New Product Introduction (NPI) processes, including transfer from R&D to production.
  • Optimize manufacturing processes, including the design and development of production equipment and jigs.
  • Writing manufacturing documentation
  • Provide production floor support through effective problem-solving and root cause analysis.
  • Collaborate with external suppliers and subcontractors to ensure quality, efficiency, and compliance.
  • Lead equipment and process qualifications (IQ, OQ, PQ)
  • Lead and implement engineering changes (ECOs) to improve design and manufacturing outcomes
  • Writing test protocols and reports.




Reports to:

Team Leader

  • B.Sc. in Mechanical, Biomedical, or Materials Engineering with a strong mechanical orientation.
  • 3-5 years of experience (medical device industry- an advantage).
  • Acquittance quality assurance and regulatory standards.
  • Proven hands-on expertise in process development.
  • Proficiency in SolidWorks (and PDM).
  • Analytical skills.
  • Good written/verbal communication skills.
  • Strong interpersonal skills with the ability to collaborate effectively across multidisciplinary teams

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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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