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- Tasks: Lead global regulatory strategy and manage international submissions for innovative medical technologies.
- Company: Forward-thinking medical device company focused on life-enhancing technologies.
- Benefits: Competitive salary up to £60k, flexible working, and ownership of projects.
- Why this job: Make a real impact on global compliance and shape the future of healthcare.
- Qualifications: Experience in regulatory affairs and strong collaboration skills required.
- Other info: Opportunity for international influence and career growth in a dynamic environment.
The predicted salary is between 43200 - 72000 £ per year.
Ready to lead global regulatory strategy? Want to shape compliance for innovative medical technologies? Looking for flexibility, ownership, and international impact?
A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals across both established and emerging markets. This is an exciting opportunity to take ownership of international regulatory submissions, collaborate with cross-functional teams, and influence strategic direction — all within a business delivering life-enhancing technologies.
Why This Role is Great
- Leading regulatory submissions and renewals across the UK, EU, US, and international markets.
- Acting as a key liaison with regulatory bodies, notified bodies, and in-country representatives.
- Supporting the creation and review of technical documentation that meets evolving global standards.
- Contributing to post-market surveillance, audits, and strategic compliance initiatives.
- Helping shape future market access plans in partnership with commercial and product teams.
Regulatory Affairs Specialist - ID45000 - Up to £60k DOE in London employer: Humand Talent
Contact Detail:
Humand Talent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Specialist - ID45000 - Up to £60k DOE in London
✨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 global regulatory standards. We recommend creating a cheat sheet of key regulations and recent changes in the medical device sector to impress your interviewers.
✨Tip Number 3
Showcase your experience with international submissions! When discussing your background, highlight specific projects where you’ve led regulatory submissions across different markets. This will demonstrate your expertise and readiness for the role.
✨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 Specialist - ID45000 - Up to £60k DOE in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Specialist role. Highlight relevant experience and skills that align with the job description, especially in regulatory submissions and compliance.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your past achievements in regulatory affairs and how they relate to the innovative medical technologies we work with.
Showcase Your Passion: Let your enthusiasm for regulatory affairs shine through! We want to see your commitment to shaping compliance and your interest in the medical device industry. A genuine passion can set you apart from other candidates.
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 this exciting opportunity to make an international impact!
How to prepare for a job interview at Humand Talent
✨Know Your Regulations
Familiarise yourself with the latest regulations and standards relevant to medical devices. This will not only show your expertise but also demonstrate your commitment to staying updated in a fast-evolving field.
✨Showcase Your Collaboration Skills
Since this role involves working with cross-functional teams, be ready to discuss examples of how you've successfully collaborated in the past. Highlight specific projects where your teamwork made a difference in achieving regulatory goals.
✨Prepare for Technical Questions
Expect questions about technical documentation and regulatory submissions. Brush up on your knowledge of the submission processes for different markets, and be prepared to explain how you ensure compliance with evolving global standards.
✨Demonstrate Strategic Thinking
Think about how you can contribute to shaping future market access plans. Be ready to share your insights on strategic compliance initiatives and how they can impact the company's growth and innovation in the medical technology space.
