Regulatory Reviewer - Medical Device Software; SaMD
Listed on 2026-11-05
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Science
Medical Device Industry, Healthcare Compliance
Scarlet is seeking a regulatory software assessors to evaluate manufacturers' software lifecycle processes and documentation for medical device software, including SaMD and AI-enabled devices, under EU MDR, UK MDR, and IEC standards. The role involves raising findings and guiding manufacturers on compliance, delivering high-quality assessments aligned with Scarlet's methodology and values.
The ideal candidate will work independently with flexible scheduling, providing clear, constructive
We would love to welcome a new Regulatory Reviewer
- Medical Device Software (SaMD) to our group in United States.
This posting is for the Regulatory Reviewer
- Medical Device Software (SaMD) role at Scarlet, based in United States.
We are looking to fill the Regulatory Reviewer
- Medical Device Software (SaMD) position at Scarlet in United States.
The Regulatory Reviewer
- Medical Device Software (SaMD) role at Scarlet is now open for applications in United States.
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