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- Tasks: Manage regulatory activities for AI-enabled medical devices and ensure compliance with global regulations.
- Company: Leading medical technology company in the UK with a focus on innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Join a pioneering team and shape the future of AI in healthcare.
- Qualifications: Five years of experience in medical device regulation and strong digital skills.
- Other info: Dynamic work environment with a commitment to innovation and excellence.
The predicted salary is between 43200 - 72000 £ per year.
A leading medical technology company in the United Kingdom is seeking an AI Medical Devices Regulatory Officer to manage regulatory activities for its portfolio of AI-enabled software medical devices. This role involves authoring technical files, offering regulatory support to product development teams, and ensuring compliance with UK, EU, and US regulations.
The ideal candidate has at least five years of experience in the medical device regulatory industry and strong digital skills.
Global AI SaMD Regulatory Lead in London employer: Odin Vision Ltd
Contact Detail:
Odin Vision Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global AI SaMD Regulatory Lead in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device regulatory field on LinkedIn. Join relevant groups and engage in discussions to get your name out there and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK, EU, and US regulations. We recommend creating a cheat sheet of key points to discuss how your experience aligns with the role of AI Medical Devices Regulatory Officer.
✨Tip Number 3
Showcase your digital skills! If you’ve worked with AI-enabled software or have experience in tech-driven environments, make sure to highlight that in conversations. It’s all about demonstrating how you can add value to the team.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications!
We think you need these skills to ace Global AI SaMD Regulatory Lead in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in the medical device regulatory industry. We want to see how your skills align with the role of Global AI SaMD Regulatory Lead, so don’t be shy about showcasing your relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about AI-enabled software medical devices and how your background makes you the perfect fit for our team. Keep it engaging and personal!
Show Off Your Digital Skills: Since this role involves working with AI and software, make sure to highlight your digital skills in both your CV and cover letter. We’re looking for someone who’s not just experienced but also tech-savvy!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts!
How to prepare for a job interview at Odin Vision Ltd
✨Know Your Regulations
Make sure you brush up on the latest UK, EU, and US regulations regarding AI-enabled medical devices. Being able to discuss specific compliance requirements will show that you’re not just familiar with the industry but also ready to tackle the challenges head-on.
✨Showcase Your Experience
Prepare to discuss your past experiences in the medical device regulatory field. Highlight specific projects where you authored technical files or provided regulatory support. Use concrete examples to demonstrate how your skills align with the role.
✨Understand the Product Development Process
Familiarise yourself with the product development lifecycle for medical devices. Be ready to explain how you can integrate regulatory considerations into each stage, ensuring compliance while supporting innovation.
✨Digital Skills Matter
Since strong digital skills are a must for this role, be prepared to discuss any relevant software tools or platforms you’ve used in your previous roles. Whether it’s data analysis tools or regulatory submission software, showing your tech-savviness will give you an edge.
