Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead regulatory affairs for innovative medical devices and manage a dynamic team.
- Company: Join a transformative device company with a global reach.
- Benefits: Fast-paced environment, leadership opportunities, and career growth.
- Why this job: Make a significant impact in a growing company focused on innovation.
- Qualifications: Regulatory experience in devices, line management skills, and relevant degree.
- Other info: Collaborate with senior leadership and work across global regions.
The predicted salary is between 36000 - 60000 £ per year.
At BioTalent, we are working with a client to fill their newly created RA manager position. They are a transformative Device company focused on a large range of products with a large customer base.
This role will offer you:
- To work in a fast-paced environment and the ability to take a huge impact.
- Work closely with senior leadership.
- A chance to lead an established team.
- Work across global regions within both NPD and NPI.
You will be responsible for:
- Both new product registrations and maintenance of existing portfolio.
- Manage a team of individual performers.
- Manage all labelling activities.
You will bring the following:
- Hands-on Regulatory experience within a device or IVD products in an ISO13485.
- Hands-on CE marking and maintenance experience.
- Ideal candidates will have US, MDSAP or other ROW experience.
- Must have previous line management experience.
- Experience within CAPA, Post marketing, NCR, Complaint management.
- BSc or MSc in a relevant Life Sciences subject.
If you want to be part of an innovative thinking, growing company where you can grow and expand your current knowledge, GET IN TOUCH - Please email me at michael.kakoullis@biotalent.com or on +447833626032 if you think you could be a good match.
Regulatory Affairs Manager in Leeds employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager in Leeds
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work at BioTalent or similar companies. A friendly chat can sometimes lead to job opportunities that aren't even advertised.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Show them you’re not just another candidate; you’re genuinely interested in their mission and how you can contribute to their success.
✨Tip Number 3
Practice your pitch! Be ready to explain your regulatory experience and how it aligns with the role. Highlight your hands-on experience with CE marking and team management to stand out.
✨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.
We think you need these skills to ace Regulatory Affairs Manager in Leeds
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Manager role. Highlight your hands-on regulatory experience, especially with device or IVD products, and don’t forget to mention your line management experience!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this fast-paced environment and how your experience aligns with the responsibilities of managing product registrations and labelling activities.
Showcase Your Team Leadership Skills: Since this role involves managing a team, make sure to highlight your previous line management experience. Share examples of how you've successfully led teams in the past and the impact you made!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get you one step closer to joining our innovative team!
How to prepare for a job interview at BioTalent
✨Know Your Regulatory Stuff
Make sure you brush up on your regulatory knowledge, especially around ISO13485 and CE marking. Be ready to discuss your hands-on experience with device or IVD products, as this will show that you’re not just familiar with the theory but have practical insights too.
✨Showcase Your Leadership Skills
Since this role involves managing a team, be prepared to share examples of your previous line management experience. Talk about how you've motivated your team, handled conflicts, or improved performance. This will demonstrate your capability to lead effectively.
✨Prepare for Global Discussions
Given that the role involves working across global regions, it’s essential to understand the nuances of different markets. Brush up on your knowledge of US, MDSAP, and other ROW regulations, and be ready to discuss how you’ve navigated these in past roles.
✨Be Ready for Scenario Questions
Expect questions around CAPA, post-marketing, NCR, and complaint management. Prepare specific scenarios where you successfully managed these processes. This will help you illustrate your problem-solving skills and your ability to handle real-world challenges in regulatory affairs.
