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- Tasks: Maintain technical files and prepare regulatory documentation for medical devices.
- Company: Leading medical device manufacturer with a focus on safety and innovation.
- Benefits: Career advancement opportunities within a collaborative team environment.
- Why this job: Join a mission-driven team ensuring safe medical devices are delivered globally.
- Qualifications: 3-5 years of experience in regulatory affairs and a degree in science or engineering.
- Other info: Dynamic role with a chance to make a real impact in healthcare.
The predicted salary is between 36000 - 60000 £ per year.
A leading medical device manufacturer is seeking a Regulatory Specialist to join its Regulatory Affairs team. This role involves maintaining technical files, preparing regulatory documentation, and supporting EU MDR and UKCA submissions.
The ideal candidate will have 3-5 years of relevant experience and a degree in a scientific or engineering discipline.
This position offers the opportunity to advance your regulatory career within a collaborative team focused on delivering safe medical devices globally.
Global Medical Device Regulatory Specialist in Cardiff employer: Walker Cole International
Contact Detail:
Walker Cole International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Medical Device Regulatory Specialist in Cardiff
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device industry on LinkedIn or at events. We can’t stress enough how valuable connections can be in landing that Regulatory Specialist role.
✨Tip Number 2
Prepare for interviews by brushing up on EU MDR and UKCA regulations. We recommend creating a cheat sheet of key points to discuss, so you can impress your interviewers with your knowledge and confidence.
✨Tip Number 3
Showcase your experience with technical files and regulatory documentation during interviews. We suggest using specific examples from your past roles to demonstrate your expertise and how you can contribute to the 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 are proactive about their job search.
We think you need these skills to ace Global Medical Device Regulatory Specialist in Cardiff
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in regulatory affairs, especially with EU MDR and UKCA submissions. We want to see how your background aligns with the role, so don’t be shy about showcasing your achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory affairs and how your skills can contribute to our mission of delivering safe medical devices globally. Keep it concise but impactful!
Showcase Your Technical Knowledge: Since this role involves maintaining technical files and preparing regulatory documentation, make sure to mention any specific tools or methodologies you’ve used. We love candidates who can demonstrate their expertise in a practical way!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Walker Cole International
✨Know Your Regulations
Make sure you brush up on the EU MDR and UKCA regulations before your interview. Being able to discuss these in detail will show that you’re not just familiar with the requirements but also passionate about compliance in the medical device industry.
✨Showcase Your Experience
Prepare specific examples from your past roles where you successfully maintained technical files or prepared regulatory documentation. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your achievements.
✨Ask Insightful Questions
Come prepared with questions that demonstrate your interest in the company and the role. Inquire about their current projects related to regulatory submissions or how they ensure collaboration within the team. This shows you’re engaged and eager to contribute.
✨Emphasise Teamwork
Since this role is within a collaborative team, be ready to discuss how you’ve worked effectively with others in the past. Highlight any experiences where you’ve contributed to a team’s success, especially in a regulatory context.
