Careers

Algorithms Manager

Job description

  • Hands on position
  • Define system and algorithm requirements
  • Draft work plans
  • Management of a algorithm engineers
  • Draft literature reviews
  • Define medical regulatory requirements
  • Algorithms implementation in Matlab
  • Work with real-time software engineers in implementation of algorithms
  • Define medical data collection methods and support clinical trials processes
  • Algorithm related clinical data analysis

 

Professional requirements

  • 5+ years of experience at relevant medical device companies – mandatory
  • Managerial experience – mandatory
  • In -depth knowledge of Matlab  – mandatory
  • Knowledge and experience in C language – mandatory
  • A graduate of a university engineering degree and/or an advanced engineering degree – required
  • Experience in the development of algorithms and/or system engineering of cardiac products  – a significant advantage
  • In-depth knowledge of signal processing – must
  • Product development experience in the field of blood pressure, vital signs, heart arrythmias – a significant advantage
  • Thorough and independent
  • Ability to work in a multidisciplinary environment
  • Thorough, effective and independent
  • Excellent people skills
  • Willingness to work hard

 

Geographical location: Northern Caesarea Industrial Park, close to the train station

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Mobile React Native developer for CardiacSense (Medical Device)

job description

  • Development of a mobile app for a medical product
  • React Native development environment
  • Development of parts of the app in Native Android / iOs
  • Development of SDK

 

Professional requirements

  • Minimum2 years experience in React Native- must
  • Extensive knowledge and experience in JavaScript– must
  • Proven experience in developing applications in React Native and native Android and iOs – must
  • Knowledge and experience in BLE communication applications – a must
  • Experience in Redux technology
  • Experience in developing medical products – an advantage
  • Knowledge of medical devices compliance requirements, such as HIPAA, FDA CFR part 11-  Advantage
  • Languages: Hebrew and English at a very good level (both speaking and writing)
  • Ability to work in a team, independent, excellent people skills
  • Fast learning ability
  • Willingness to work hard

 

Geographical location: Caesarea North Industrial Park, close to the train station

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Experienced cloud developer for CardiacSense (medical device)

job description

  • Development of cloud applications for a medical product
  • Development in JavaScript
  • AWS Cloud environment
  • API development for 3rd party cloud systems of customers and partners

 

Professional requirements

  • 3+ years experience in a similar position
  • Experience in developing infrastructure/native cloud applications (IAS) – a significant advantage
  • Knowledge and experience in data structures (relational & non-relational – must
  • Experience working in React Native – an advantage
  • Experience in developing medical products – an advantage
  • Team management experience/project management – an advantage
  • Experience in Redux technology
  • Knowledge of software compliance requirements for medical products, such as : HIPAA, FDA CFR part 11-  an advantage
  • Languages: Hebrew and English at a very good level (both speaking and writing)
  • Ability to work in a team, independent, excellent people skills
  • Fast learning ability
  • Willingness to work hard

 

Geographical location: Caesarea North Industrial Park, close to the train station

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Medical Device Regulatory Affairs assistant / Submission Officer / Clinical affairs assistant

Job description

  • Provide clerical support to the Clinical and Regulatory Affairs team.
  • Assist in medical device regulatory submissions, registration and maintenance, in multiple territories. Liaise with external consultants, registration and regulatory bodies with respect to registration needs.
  • Perform other regulatory or clinical activities assigned as appropriate.
  • Perform Ad-hoc duties with regards to clinical and regulatory affairs, as assigned.

Professional requirements

  • Diploma or above, with life science or related discipline preferred.
  • Minimum 1-year medical device regulatory/clinical clerical experience is preferred.
  • Fluency in English and Hebrew (written and spoken), additional languages are an advantage.
  • Self-motivated and responsible worker.
  • Ability to work under time constraints and stressful conditions.
  • Immediately available is preferred.
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