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Engineering field · Other engineering fields

Medical technology

Engineers for the development of medical devices, risk management and documentation for approval under the MDR.

Typical tasks

  • Development of devices and components
  • Risk management to ISO 14971
  • Technical documentation under the MDR
  • Verification and validation

Focus areas

Focus: Medical devices
Focus: Implants and instruments
Focus: Regulatory affairs

Standards and regulations

What engineers in Medical technology should know depending on the task. Enter the ones important for your project as requirements; the matching checks each one.

  • MDR (EU) 2017/745 and IVDR (EU) 2017/746
  • EN ISO 13485 quality management
  • EN ISO 14971 risk management
  • IEC 60601 electrical safety and IEC 62304 software
  • IEC 62366 usability

Frequently asked questions

Do freelancers help with technical documentation under the MDR?

Yes. Typical are risk management files to ISO 14971, verification and validation plans, software documentation to IEC 62304 and support with the technical documentation. The assessment by the notified body remains the manufacturer's responsibility.

How do I find freelance engineers for Medical technology?

Post your project for free and enter the task, tools (e.g. SolidWorks, Creo, Altium Designer) and standards. We compare it with the profiles in the pool and suggest the best matches with Match-Score and missing requirements. Your company name stays hidden.