Biomedical Engineer and Analyst

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12012en
  1. Contract
  2. English
  3. Mid-Senior level
  4. Digital & Technology
  5. Basel
  6. Healthcare & Life Sciences

Skills

Biomedical, Data Analysis, 2D math, 3D math, Computer Vision, Virtual Reality Technologies, Python, Matlab, English

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About our client:
Our client is a global leader within the Pharmaceutical Industry. On behalf of our client, Swisslinx is currently looking for a Biomedical Engineer and Analyst to join a 1 year contract in Basel area.

Your responsibilities:
- Support the data engineering and data analysis activities around the development of new clinical endpoints for ophthalmology based on AR/VR technologies
- Formalize and plan a data analysis roadmap capturing the requirements from different stakeholders in the project (clinical, regulatory, software development, etc)
- Implement the work packages in the roadmap to deliver results
- Leverage the high quality data to develop new clinical end points and compare them to current recognized gold standard
- Interact with stakeholders from different domains and with different background to guarantee the success of the project


Your background:
- 5+ years of experience working on biomedical related data analysis topics
- University degree in physics, mathematics, engineering, natural science or informatics
- Excellent understanding of the practical applications of 2D and 3D math (linear algebra, matrix multiplication, quaternions, etc)
- Ability to understand and apply computer vision concepts (contrast, luminosity, etc.)
- Previous experience with augmented and virtual reality technologies / Previous experience with Unity of similar 3D engines
- Profound knowledge of Python or Matlab
- Fluency in English, written and verbal

Nice to have:
- Experience with C\C++
- Experience with signal processing
- Experience working with 3D content and content creation tools
- Experience with Agile Scrum environment
- Previous hands-on clinical experience with Multiple Sclerosis or in ophthalmology
- Good understanding of regulatory frameworks and compliance implications (e.g. GxP, GDPR)
- Experience with remote patient monitoring
- Experience in experimental/clinical study design

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