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- Tasks: Review and rate AI-generated outputs for medical device criteria.
- Company: Join Medcase, a leader in healthcare AI research.
- Benefits: Fully remote work with flexible hours and a clear project scope.
- Why this job: Shape the future of AI in healthcare and make a real impact.
- Qualifications: UK-based regulatory professional with SaMD experience and strong knowledge of UK/EU frameworks.
- Other info: Collaborate with global experts in a structured, research-driven environment.
The predicted salary is between 13 - 16 £ per hour.
Medcase is partnering with a leading client on a high-impact research initiative focused on generative AI and Software as a Medical Device (SaMD)—and we're looking for UK-based health regulatory specialists to contribute their expertise.
About the Project
- Goal: Evaluate and classify AI-generated outputs to assess whether they meet medical device criteria, supporting the responsible development of healthcare AI.
- Scope: Structured review of model-generated responses following established regulatory evaluation guidelines.
- Time commitment: Approximately 24–32 total hours, including onboarding, calibration, and evaluation work.
- Start date: Upcoming start (onboarding begins once selected).
- Location: Fully remote with flexible, asynchronous participation.
What You'll Do
- Review and rate AI-generated responses using health regulatory criteria.
- Apply SaMD and AI regulatory frameworks to diverse scenarios.
- Ensure consistency and quality across evaluations.
- Participate in calibration and feedback discussions as needed.
Who You Are
- UK-based health regulatory professional with SaMD experience.
- Background in Regulatory Affairs, Health Sciences, Medicine, or a related field.
- Strong knowledge of UK and/or EU regulatory frameworks (MHRA experience is a plus).
- Comfortable working independently in a structured, research-driven environment.
Why Join Medcase?
- Contribute to the responsible development of AI in healthcare.
- Apply your regulatory expertise beyond traditional submissions.
- Collaborate with a global network of health and technology experts.
- Flexible, remote work with a clearly defined scope.
Interested? Apply now and help shape how AI-powered medical technologies are evaluated and regulated for the future.
UK Health Regulatory Specialist – AI & Software as a Medical Device (SaMD) in Newcastle upon Tyne employer: Medcase
Contact Detail:
Medcase Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land UK Health Regulatory Specialist – AI & Software as a Medical Device (SaMD) in Newcastle upon Tyne
✨Tip Number 1
Network like a pro! Reach out to professionals in the health regulatory field, especially those with SaMD experience. Use platforms like LinkedIn to connect and engage with them—ask questions, share insights, and show your enthusiasm for the industry.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK and EU regulatory frameworks. Be ready to discuss how you would apply these frameworks to AI-generated outputs. We want to see your expertise shine through!
✨Tip Number 3
Showcase your skills through practical examples. When discussing your experience, highlight specific projects where you evaluated medical devices or worked with AI in healthcare. This will help us see how you can contribute to our mission.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our team and contributing to the responsible development of AI in healthcare.
We think you need these skills to ace UK Health Regulatory Specialist – AI & Software as a Medical Device (SaMD) in Newcastle upon Tyne
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience with SaMD and regulatory frameworks. We want to see how your background aligns with the role, so don’t hold back on showcasing your relevant skills!
Showcase Your Expertise: In your application, emphasise your knowledge of UK and EU regulatory frameworks. We’re looking for someone who can navigate these guidelines effortlessly, so let us know about any specific experiences you have in this area.
Be Clear and Concise: When writing your application, keep it straightforward and to the point. We appreciate clarity, so avoid jargon and make sure your key points stand out. This will help us understand your qualifications quickly!
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Medcase
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of UK and EU regulatory frameworks, especially around SaMD. Be ready to discuss specific examples from your experience that demonstrate your understanding of these regulations.
✨Familiarise Yourself with AI in Healthcare
Since the role focuses on generative AI, it’s crucial to understand how AI impacts medical devices. Research recent developments in AI and be prepared to talk about how they relate to regulatory practices.
✨Prepare for Scenario-Based Questions
Expect to face questions that require you to apply regulatory frameworks to hypothetical situations. Practise articulating your thought process clearly and logically, as this will showcase your analytical skills.
✨Show Your Collaborative Spirit
This role involves calibration and feedback discussions, so highlight your ability to work well in a team. Share examples of past collaborations where you contributed to achieving a common goal, especially in a remote setting.
