You will be responsible for monitoring global regulatory changes, interpreting complex technical requirements, and ensuring the accuracy and consistency of CRI’s Medical Device and IVD content
Job Summary
You will be responsible for monitoring global regulatory changes, interpreting complex technical requirements, and ensuring the accuracy and consistency of CRI’s Medical Device and IVD content.
Provide authoritative subject-matter expertise to guide, validate, and enhance AI-assisted content generation processes.
As part of Regulatory Market Access, the Regulatory Intelligence team consists of subject-matter experts responsible for monitoring and curating global regulatory content across the full medical product, medical device and IVD lifecycle.
Matching Summary
You will be responsible for monitoring global regulatory changes, interpreting complex technical requirements, and ensuring the accuracy and consistency of CRI’s Medical Device and IVD content.