Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead regulatory functions and ensure compliance with EU MDR and FDA for medical devices.
- Company: A growing medical device company based in Nottingham.
- Benefits: Full-time position with opportunities to influence the regulatory landscape.
- Why this job: Make a significant impact in the medical device industry and shape regulatory practices.
- Qualifications: Bachelor’s degree and 5+ years of experience with Class II medical devices.
- Other info: Join a dynamic team and advance your career in a vital sector.
The predicted salary is between 36000 - 60000 £ per year.
A growing medical device company in Nottingham is seeking a Regulatory Specialist to own regulatory functions and ensure compliance with EU MDR and FDA requirements. The role involves managing regulatory submissions and serving as the key contact with regulators.
Candidates should have a Bachelor’s degree and over 5 years of hands-on experience with Class II medical devices. This is a full-time position offering the chance to significantly influence the regulatory landscape within the company.
Regulatory Lead for Class II Medical Devices & EU MDR in Nottingham employer: Neupulse
Contact Detail:
Neupulse Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Lead for Class II Medical Devices & EU MDR in Nottingham
✨Tip Number 1
Network like a pro! Reach out to industry professionals on LinkedIn or attend local meetups. We can’t stress enough how personal connections can open doors for you in the regulatory field.
✨Tip Number 2
Prepare for interviews by brushing up on EU MDR and FDA regulations. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for tailored job listings that fit your skills in regulatory affairs.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm and professionalism, which is crucial in the regulatory landscape.
We think you need these skills to ace Regulatory Lead for Class II Medical Devices & EU MDR in Nottingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with Class II medical devices and compliance with EU MDR and FDA requirements. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects!
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 expertise can help us navigate the complexities of medical device regulations. Keep it engaging and personal!
Showcase Your Achievements: When detailing your experience, focus on specific achievements that demonstrate your impact in previous roles. Whether it’s successful submissions or improved compliance processes, we love to see quantifiable results!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves!
How to prepare for a job interview at Neupulse
✨Know Your Regulations
Make sure you brush up on the EU MDR and FDA requirements specific to Class II medical devices. Being able to discuss these regulations confidently will show that you’re not just familiar with them, but that you can navigate them effectively.
✨Showcase Your Experience
Prepare to share specific examples from your past roles where you successfully managed regulatory submissions or dealt with regulators. Highlighting your hands-on experience will demonstrate your capability and readiness for the role.
✨Understand the Company’s Products
Research the company’s product line and any recent news related to their regulatory activities. This knowledge will help you tailor your answers and show genuine interest in how you can contribute to their success.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s regulatory strategy and challenges they face. This not only shows your enthusiasm for the role but also your strategic thinking regarding regulatory compliance.
