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.

About the Job

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.

Reports to: Director of Engineering

 

Responsibilities

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.

 

Qualifications

• B.Sc in Mechanical Engineering-must.

• Recommended three years of experience in the medical device industry.

• Proficiency in Solid works (and PDM).

• Analytical skills.

• Good written/verbal communication skills.

 

    Resume*

    About the Job

    We are currently seeking a pre-clinical associate who will participate in in-vivo studies performed with the Company’s products, both locally and abroad (work-related travel up to 50% abroad).

    Reports to: Sr. Director of Pre-Clinical

     

    Responsibilities

    • Perform and monitor animal studies for both R&D and pre-submission/submission activities.

    • Document and report online information during studies.

    • Maintain accurate records of all testing data and results in the specified forms (paper and electronic) in accordance with the company’s guidelines.

    • Handle biological tissues and blood samples.

    • Provide general assistance in pre-clinical assignments.

     

    Qualifications

    • BSc or MSc in Biology, Biomedical Engineering, Veterinary Medicine, or a related field – must.

    • Ability to travel periodically for 1-2 weeks at a time – must.

    • Ability to work nights periodically for 1-2 weeks at a time – must.

    • Two years of experience with pre-clinical studies – advantage.

    • Dedication and proactiveness, with the ability to complete tasks in urgent and stressful situations.

    • Highly creative, adaptive, and flexible thinker.

    • Excellent proficiency in English (oral and written).

    • Strong ability to handle complex situations.

     

      Resume*

      About the Job

      We are looking for a dynamic and experienced Project Manager who will be part of the PMO team.

      Reports to: Engineering  & Project Manager

       

      Responsibilities

      Assist with project planning, coordination, and execution:

      • Set a timeline and monitor project deliverables.

      • Update relevant stakeholders or team members on the project’s progress.

      • Coach and support project team members with tasks you assign them.

      • Develop detailed project plans, define scope and objectives, and coordinate activities to ensure successful execution within established timelines.

      • Integration of multidisciplinary systems, including mechanics, materials, electronics, and software.

      • Collaborate with multidisciplinary teams, including R&D, engineering, QA/R ,clinical, and manufacturing.

      • Identification of bottlenecks in existing work processes and definition of appropriate solutions in collaboration with the professional team

       

      Qualifications

      • B.Sc. Engineer in mechanical/ biomedical/ materials science (or other relevant degree).

      • 4+ years of experience in a similar role in a medical device company – must.

      • Experience with the entire product lifecycle, from early development stages to complete transfer for production  must.

      • High hands-on technical skills and experience in CAD (SolidWorks – Model & Drawings) are advantages.

      • 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.

       

        Resume*

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