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- Tasks: Develop regulatory strategies and manage global product license registrations.
- Company: Leading healthcare organisation in the UK with a focus on innovation.
- Benefits: Competitive salary, professional development, and a chance to make an impact.
- Why this job: Join a dynamic team and shape the future of medical devices.
- Qualifications: Strong knowledge of CE and FDA submissions, plus excellent technical writing skills.
- Other info: Opportunity to work in an innovative sector with career growth potential.
The predicted salary is between 36000 - 60000 £ per year.
A leading healthcare organisation in the UK is seeking a Regulatory Affairs Officer to develop regulatory strategies and manage product license registrations globally. You'll prepare documentation, advise teams, and ensure compliance with standards like ISO13485 and FDA regulations.
Strong knowledge of CE and FDA submissions is crucial, along with excellent technical writing skills and attention to detail. This role offers the chance to impact a dynamic team within an innovative sector.
Global Regulatory Affairs Lead – Medical Devices employer: Jobster
Contact Detail:
Jobster Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Regulatory Affairs Lead – Medical Devices
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of CE and FDA submissions. We recommend creating a list of common interview questions and practising your responses, especially around compliance and technical writing skills.
✨Tip Number 3
Showcase your attention to detail! During interviews, share examples of how you’ve ensured compliance with standards like ISO13485. We want to see how you can bring that meticulousness to our team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Global Regulatory Affairs Lead – Medical Devices
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with regulatory strategies and product license registrations. We want to see how your skills align with the requirements, especially your knowledge of CE and FDA submissions.
Show Off Your Technical Writing Skills: Since excellent technical writing is key for this role, include examples of documentation you've prepared in the past. We love seeing clear, concise writing that demonstrates your attention to detail.
Highlight Compliance Experience: Emphasise any experience you have with compliance standards like ISO13485 and FDA regulations. We’re looking for candidates who can navigate these complexities with ease, so don’t hold back!
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 this exciting opportunity in our dynamic team.
How to prepare for a job interview at Jobster
✨Know Your Regulations
Make sure you brush up on the latest ISO13485 and FDA regulations before your interview. Being able to discuss these standards confidently will show that you’re not just familiar with them, but that you can apply this knowledge practically.
✨Showcase Your Technical Writing Skills
Prepare examples of your technical writing from previous roles. Whether it’s documentation for product registrations or compliance reports, having tangible examples ready will demonstrate your expertise and attention to detail.
✨Understand the Company’s Products
Research the healthcare organisation’s products and their regulatory pathways. This will allow you to tailor your answers to how you can specifically contribute to their goals and challenges in regulatory affairs.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific regulatory challenges. Think through potential scenarios related to CE and FDA submissions, and be ready to articulate your thought process and problem-solving skills.
