Medtech Engineer

Teoresi Group

Indiana (PA)

On-site

USD 60,000 - 80,000

Full time

14 days+

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Job summary

Teoresi Group in Indiana is seeking engineers to support the development, integration, and validation of medical devices and healthcare systems. The role involves utilizing engineering tools for testing, collaborating on software engineering activities, and ensuring compliance with medical regulations.

Ideal candidates will have a degree in Biomedical Engineering or a related field, strong analytical skills, and experience in system validation. The position contributes significantly to healthcare innovation and quality assurance.

Qualifications

  • Support development, integration, and validation of medical devices and healthcare systems.
  • Ensure compliance with relevant medical regulations and standards (e.g., ISO 13485, IEC 62304).

Responsibilities

  • Utilize engineering tools and methodologies for testing, data analysis, and system verification.
  • Collaborate on software and/or system engineering activities, including requirements definition and documentation.
  • Contribute to system integration activities involving hardware, software, and medical devices.

Skills

Strong analytical and problem-solving skills
Experience in software and/or system validation activities

Education

Bachelor’s or Master’s degree in Biomedical Engineering, Electrical Engineering, Computer Engineering, or related field

Job description

Company Teoresi Group -> Teoresi SA | Switzerland
Job requirements
  • Support development, integration, and validation of medical devices and healthcare systems
  • Utilize engineering tools and methodologies for testing, data analysis, and system verification
  • Collaborate on software and/or system engineering activities, including requirements definition and documentation
  • Ensure compliance with relevant medical regulations and standards (e.g., ISO 13485, IEC 62304)
  • Contribute to system integration activities involving hardware, software, and medical devices
  • Maintain documentation of development activities, test procedures, and results in line with quality standards
  • Generate reports to communicate findings, support regulatory submissions, and drive continuous improvement
Preferential position requirements
  • Bachelor’s or Master’s degree in Biomedical Engineering, Electrical Engineering, Computer Engineering, or related field
  • Background in medtech or healthcare industry is a plus
  • Strong analytical and problem-solving skills
  • Experience in software and/or system validation activities
  • Familiarity with medical device regulations and quality processes is considered a plus
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