Medical Device Algorithm Engineer – Patient Monitoring

MS0275 GE Healthcare Finland Oy

Helsinki

On-site

EUR 60,000 - 90,000

Full time

5 days ago
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Job summary

GE HealthCare Helsinki is seeking an enthusiastic Algorithm Developer to advance patient monitoring software by designing, implementing, and maintaining algorithms for vital signs monitoring, data analytics, and AI/ML applications.

You will collaborate with clinicians, algorithm and software developers, system engineers and product managers across the full lifecycle, ensuring regulatory documentation and rigorous testing.

Qualifications

  • MSc degree in a related discipline.
  • Experience in algorithm development, data analysis, signal processing or AI/ML.
  • Experience with Python and/or Matlab for development and analysis.
  • Programming skills in C/C++.
  • Hands-on experience using AI development tools for data analysis, software development and testing.
  • Strong analytical and problem-solving skills.
  • Ability to work effectively in a multidisciplinary team.
  • Strong communication skills in English, both verbal and written.

Responsibilities

  • Develop and maintain algorithms for vital signs monitoring.
  • Perform data analysis and algorithm performance testing.
  • Support physiological data collection, dataset validation, and clinical study analysis.
  • Collaborate with algorithm & software developers, system engineers, clinicians, and product managers.
  • Contribute to product verification, validation, and regulatory documentation.
  • Ensure compliance with applicable medical device standards and quality processes.

Skills

Python
Matlab
C/C++
Data analysis
Signal processing
AI/ML applications
English communication

Education

MSc in Biomedical Engineering

Tools

AI development tools

Job description

GE HealthCare Helsinki is seeking an enthusiastic Algorithm Developer to advance patient monitoring software by designing, implementing, and maintaining algorithms for vital signs monitoring, data analytics, and AI/ML applications.

You will collaborate with clinicians, algorithm and software developers, system engineers and product managers across the full lifecycle, ensuring regulatory documentation and rigorous testing.

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