CyOne Security AG
Steinhausen
Software in the Context of the Medical Device Regulation (MDR)
- 07 August 2026
- 100%
- Permanent position
- Steinhausen
Job summary
Explore the intersection of software and Medical Device Regulation (MDR). This is a great opportunity to understand compliance and enhance your knowledge.
Tasks
- Learn how software is classified under MDR regulations.
- Discover the evaluation process for software conformity.
- Understand requirements for software updates and maintenance.
Skills
- Knowledge of medical devices and software compliance is essential.
- Familiarity with Medical Device Regulation (MDR).
- Understanding of software evaluation processes.
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About the job
WHITEPAPER
Software in the Context of the Medical Device Regulation (MDR)
Anyone placing a medical device on the market in Switzerland or an EU contracting state, or intending to operate it without placing it on the market, must demonstrate its conformity with the Medical Device Regulation (MDR).
In an assessment procedure, the conformity of the product must be evaluated and determined.
Download the whitepaper now and get answers to the questions
- What does this mean for software?
- How is software classified and assessed in the context of the MDR?
- What are the specific requirements for software updates?
Obtain the knowledge update "Software in the Context of the Medical Device Regulation (MDR)" as a PDF
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