Careers

We are hiring!

Position 1: Algorithm Developer

Qualifications

  • MSc / PhD in Exact Sciences
  • At least 3 years of experience at machine learning algorithms, in computer vision context

Skills

  • High proficiency in MATLAB
    Advantage: C++/C# proficiency
    Familiarity with: Graph Theory; Optimization; Deep learning; 3D reconstruction;
  • Excellent communication,Likes to be challenged,Independent and capable of leading projects

Position 2: Software Developer

Qualifications

  • Degree in SW Engineering or Computer Sciences
  • At least 3 years of experience in SW development of complex systems, preferably in medical imaging

Skills

  • High proficiency in C++/C#
  • Excellent communication skills
  • Independent with real hands-on drive
  • Advantage: familiarity with MATLAB
    Advantage: experience in 3D rendering

Position 3: Application/Clinical Engineer

Job Responsibilities

  • Be part of a R&D team in the field ofcardiovascular imaging
  • Use software and mathematical models to design, develop and test new algorithms
  • Support regular testing activities
  • Coordinate software updates with developers team
  • Prepare reports and manuscripts for publication

 

Education & Experience

  • Degree in bio-medical engineering or medical sciences or health related field
  • At least 2 years’ experience in biomedical engineering or clinical science
  • Prior clinical specialist experience in the field of Cardiac CT – highly preferred
  • Experience working directly on product development
  • Previous system V&V experience
  • Experience utilizing Matlab for analysis

Skills 

  • Experience with cardiovascular medical devices
  • Strong computer and technological skills
  • Ability to write reports and effectively present information
  • Ability to prioritize multiple tasks and achieve project timelines
  • Able to take initiative and work independently

Position 4: CRA

Responsibilities

  • Being involved in all stages of a clinical trial, including identifying an investigational site and setting up, initiating, monitoring and closing down the trial; Supervising the conduct of clinical studies: act as liaison between site personnel and the sponsor; performs monitoring in the field; ensures compliance with protocols, regulatory requirements, and GCP.
  • Designing CRFs
  • Managing regulatory authority and EC/IRB applications and approvals;

 

Work experience

  • A minimum of 2 years as a CTA or CTA in a medical device company or working on medical device trials is a must

Skills

  • excellent communication skills (both written and oral) in English and Hebrew.
  • and the ability to build effective relationships with trial study staff;
  • numeracy and an eye for detail;
  • the ability to multi-task;
  • good organizational, IT and administrative skills;
  • Understand the importance of GCP;

Position 5: SQA

Responsibilities

  • entire software testing – currently manual and in the future partly automatic. (not an automation developer position)
  • STD and ATP maintenance.

 

Required skills/experience

  • 3+ years at a QA position

Skills

  • Bio-engineering degree, or other background in medical, familiarity with coronary anatomy
  • Advantage: familiarity with CE/FDA regulatory requirements.
  • Excellent communication
  • Likes to be challenged

If you think either of these positions is right for you