Software as Medical Device QARA Consultant (3-6 Month Contract, Remote)
A variety of soft skills and experience may be required for the following role Please ensure you check the overview below carefully.
We're seeking an experienced QARA Consultant to work on multiple SaMD and AIaMD project on quality and regulatory activities. You'll own end-to-end regulatory submissions (CE & FDA), support QMS implementation.
Key requirements:
* Proven experience with CE marked & FDA-authorised SaMD/AIaMD products
* Strong knowledge of ISO 13485, ISO 14971, IEC 62304/82304/62366
* Confident leading submissions, client engagements, and multiple projects
What's on offer:
* Possible extensions
* Flexible rate
* Remote working
Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. xsngvjr If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.
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