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- Tasks: Lead regulatory activities for Class II medical devices and ensure compliance with EU MDR and FDA.
- Company: Growing medical device company based in Nottingham with a focus on innovation.
- Benefits: Competitive salary, health benefits, and the chance to make a real impact.
- Why this job: Join a meaningful role where your expertise shapes the future of healthcare.
- Qualifications: Bachelor's degree and over 5 years of experience in Regulatory Affairs.
- Other info: Collaborative environment with opportunities for professional growth.
The predicted salary is between 42000 - 60000 £ per year.
A growing medical device company based in Nottingham is seeking a Regulatory Specialist to take ownership of regulatory activities. This role involves managing submissions for Class II medical devices, ensuring compliance with EU MDR and FDA regulations, and working closely with engineering and clinical teams.
Ideal candidates will have a Bachelor's degree and over 5 years of hands-on experience in Regulatory Affairs. This is an opportunity to make a significant impact in a meaningful role.
Regulatory Lead - Class II Medical Devices (EU MDR & FDA) in Nottingham employer: Neupulse
Contact Detail:
Neupulse Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Lead - Class II Medical Devices (EU MDR & FDA) in Nottingham
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device industry on LinkedIn. Join relevant groups and engage in discussions to get your name out there and show your expertise.
✨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 how your experience aligns with the role's requirements.
✨Tip Number 3
Don’t just apply; follow up! After submitting your application through our website, send a friendly email to express your enthusiasm for the role. It shows initiative and keeps you on their radar.
✨Tip Number 4
Showcase your impact! When discussing your past roles, focus on specific achievements in regulatory affairs that demonstrate your ability to manage submissions effectively and ensure compliance.
We think you need these skills to ace Regulatory Lead - Class II Medical Devices (EU MDR & FDA) in Nottingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs, especially with Class II medical devices. We want to see how your background aligns with the EU MDR and FDA regulations, so don’t hold back on those details!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory work and how your skills can help us at StudySmarter. Be specific about your achievements and how they relate to the role.
Showcase Your Teamwork Skills: Since this role involves working closely with engineering and clinical teams, make sure to highlight any collaborative projects you've been part of. We love seeing candidates who can work well with others and drive results together!
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 shows you’re keen on joining our team!
How to prepare for a job interview at Neupulse
✨Know Your Regulations
Make sure you brush up on the EU MDR and FDA regulations relevant to Class II medical devices. Being able to discuss specific compliance requirements and how they apply to the role will show that you're not just familiar with the basics, but that you truly understand the intricacies of regulatory affairs.
✨Showcase Your Experience
Prepare to share concrete examples from your past roles where you've successfully managed submissions or navigated regulatory challenges. Highlighting your hands-on experience will demonstrate your capability and confidence in handling the responsibilities of the position.
✨Collaborate and Communicate
Since this role involves working closely with engineering and clinical teams, be ready to discuss how you've effectively collaborated with cross-functional teams in the past. Emphasise your communication skills and how you can bridge the gap between technical and regulatory aspects.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's current projects, regulatory challenges they face, or their approach to compliance. This not only shows your genuine interest in the role but also gives you a chance to assess if the company aligns with your career goals.
