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- Tasks: Manage compliance with FDA, Health Canada, and EU regulations for medical products.
- Company: Leading medical technology company based in Bedford, UK.
- Benefits: Engage directly with regulatory agencies and enhance your professional skills.
- Why this job: Make a real impact in the medical field while ensuring product safety and compliance.
- Qualifications: Experience in regulatory affairs and strong communication skills.
The predicted salary is between 36000 - 60000 £ per year.
A leading medical technology company based in Bedford, UK is looking for a regulatory affairs professional to manage compliance with US FDA, Health Canada, and EU regulations. The role involves preparing regulatory submissions and reviewing product labeling for compliance.
Ideal candidates will have experience in overseeing regulatory activities related to medical products and excellent communication skills. This position offers an opportunity to engage with regulatory agencies directly.
Strategic Regulatory Lead — FDA/EC IVD Submissions in Bedford employer: Werfen
Contact Detail:
Werfen Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Strategic Regulatory Lead — FDA/EC IVD Submissions in Bedford
✨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 when it comes to landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of FDA and EU regulations. We recommend creating a cheat sheet of key points to discuss, so you can impress your interviewers with your expertise and confidence.
✨Tip Number 3
Showcase your communication skills! During interviews, be ready to explain complex regulatory concepts in simple terms. We want to see how well you can engage with others, especially when dealing with regulatory agencies.
✨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 Strategic Regulatory Lead — FDA/EC IVD Submissions in Bedford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with FDA, Health Canada, and EU regulations. We want to see how your background aligns with the role of Strategic Regulatory Lead, 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 skills can help us navigate compliance challenges. Keep it concise but impactful!
Showcase Communication Skills: Since this role involves direct engagement with regulatory agencies, we need to see your communication prowess. Highlight any experiences where you’ve successfully communicated complex information to diverse audiences.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and get to know you better!
How to prepare for a job interview at Werfen
✨Know Your Regulations
Make sure you brush up on the latest US FDA, Health Canada, and EU regulations related to IVD submissions. Being able to discuss specific compliance requirements will show that you're not just familiar with the rules but also passionate about ensuring adherence.
✨Prepare Your Success Stories
Think of concrete examples from your past experience where you've successfully managed regulatory submissions or navigated complex compliance issues. This will help you demonstrate your expertise and problem-solving skills during the interview.
✨Practice Your Communication Skills
Since excellent communication is key for this role, practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing technical topics in an accessible way.
✨Engage with Regulatory Agencies
Show your enthusiasm for direct engagement with regulatory agencies by preparing questions about their processes. This not only demonstrates your interest in the role but also your proactive approach to building relationships in the regulatory landscape.
