Job Description
We are looking for a Senior Medical Devices Specialist with strong expertise in Medical Devices (MD), In Vitro Diagnostics (IVD), and Combination Products to join our Life Sciences Regulatory Intelligence team. The ideal candidate will have a solid background in medical device regulatory affairs, quality systems, or compliance, and a passion for delivering high quality, accurate, and actionable regulatory intelligence.
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. Your ability to apply subject matter expertise, work within AI enhanced editorial workflows, and collaborate across global teams will be essential to supporting users navigating evolving regulatory frameworks.
About You – experience, education, skills, and accomplishments
Bachelor’s degree in a relevant scientific, engineering, or technological fi...
Apply for this Position
Ready to join Clarivate? Click the button below to submit your application.
Submit Application