At a Glance
- Tasks: Lead the EU regulatory strategy for a groundbreaking Class III medical device.
- Company: Join a global leader in healthcare innovation and technology.
- Benefits: Competitive salary, travel opportunities, and a chance to shape the future of medical devices.
- Other info: Dynamic role with opportunities for professional growth and international collaboration.
- Why this job: Make a real impact in healthcare by driving regulatory excellence for innovative products.
- Qualifications: Experience in regulatory affairs and a passion for medical technology.
The predicted salary is between 48000 - 72000 £ per year.
Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business continues to invest heavily in next-generation technologies and regulatory excellence.
We have a brand new opportunity for a Regulatory Affairs Manager to lead the EU Regulatory Strategy for a brand new Class III medical device. This is a strategically significant role within a highly experienced global regulatory function. While based in Maidenhead, you would need to travel to the Oxford site twice a week.
As the Regulatory Affairs Manager, you will define and drive the EU regulatory pathway under MDR 2017/745 for a new product programme. You will lead regulatory strategy development from early-stage development through to submission and approval, ensuring alignment with global regulatory, clinical and R.
Regulatory Affairs Manager employer: Cure Talent
As a leading global healthcare organisation, we pride ourselves on fostering a dynamic and inclusive work culture that prioritises innovation and employee development. Our Maidenhead location offers a collaborative environment where you can thrive professionally while contributing to groundbreaking medical advancements. With robust growth opportunities and a commitment to regulatory excellence, joining us as a Regulatory Affairs Manager means being part of a team that is dedicated to making a meaningful impact in the healthcare sector.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs Manager
✨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 EU regulations and the specific requirements for Class III medical devices. We recommend practising common interview questions with a friend to boost your confidence.
✨Tip Number 3
Showcase your expertise! During interviews, highlight your experience with regulatory strategy development and any successful submissions you've led. We want to see how you can bring value 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 Regulatory Affairs Manager
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Regulatory Affairs Manager role. Highlight your experience with EU regulatory pathways and any relevant medical device knowledge. We want to see how your background aligns with our needs!
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 you can contribute to our innovative projects. Keep it concise but impactful – we love a good story!
Showcase Your Achievements:Don’t just list your responsibilities; showcase your achievements in previous roles. Quantify your successes where possible, like successful submissions or approvals. We’re looking for results-driven individuals who can make a difference!
Apply Through Our Website:We encourage you to apply 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. Plus, it’s super easy!
How to prepare for a job interview at Cure Talent
✨Know Your Regulations
Make sure you brush up on the latest EU regulations, especially MDR 2017/745. Being able to discuss these in detail will show your expertise and commitment to the role.
✨Showcase Your Strategic Thinking
Prepare examples of how you've developed regulatory strategies in the past. Highlight your ability to align regulatory pathways with clinical and global strategies, as this is crucial for the position.
✨Demonstrate Your Leadership Skills
As a Regulatory Affairs Manager, you'll need to lead teams and projects. Be ready to share experiences where you've successfully led a team or influenced stakeholders to achieve regulatory goals.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's regulatory challenges and future innovations. This shows your genuine interest in the role and helps you understand how you can contribute effectively.
