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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 in Edinburgh employer: Jobster
Contact Detail:
Jobster Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Regulatory Affairs Lead – Medical Devices in Edinburgh
✨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 answers. This will help you feel confident and ready to impress!
✨Tip Number 3
Showcase your technical writing skills! Bring along samples of your previous work or create a portfolio that highlights your attention to detail. We want to see how you can communicate complex regulatory information clearly.
✨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 are proactive about their job search!
We think you need these skills to ace Global Regulatory Affairs Lead – Medical Devices in Edinburgh
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 this role requires excellent technical writing, 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 product line and any recent innovations. This will help you tailor your answers and show that you’re genuinely interested in how you can contribute to their regulatory strategies.
✨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 discuss your thought process and problem-solving skills.
