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- Tasks: Drive EU regulatory projects and improve internal processes in a hands-on role.
- Company: Join a dynamic team focused on innovation in regulatory affairs.
- Benefits: Real ownership, growth opportunities, and collaboration with senior leadership.
- Other info: Ideal for curious individuals eager to make an impact.
- Why this job: Shape the future of regulatory practices while working across diverse projects.
- Qualifications: 3-5 years in Regulatory Affairs with a proactive mindset and versatility.
The predicted salary is between 55000 - 65000 £ per year.
A hands-on EU Regulatory Affairs role for someone who wants more than just execution – a chance to take ownership, work broadly across regulatory and pharma projects, and help build how regulatory is done internally.
The opportunity:
- You will join a growing regulatory set up where parts of the work are currently handled externally, and where there is a clear ambition to strengthen internal ownership.
- As a Deputy to the Head of Regulatory Affairs, you will work across the full regulatory lifecycle – from submissions to lifecycle management – while taking a proactive role in driving projects, improving processes, and shaping the function going forward.
This role is ideal for someone who is hands-on, curious, and not limited to a narrow regulatory scope.
We Would Like You to:
- Support and execute EU regulatory activities across assigned products.
- Act as internal owner toward external regulatory partners, ensuring quality and progress.
- Work with EU procedures (centralised, DCP/MRP, national) and support submissions and lifecycle activities.
- Collaborate cross-functionally with Clinical, CMC, QA, PV, and Commercial teams.
- Take initiative in projects and contribute to building and improving regulatory processes.
What We Need You To Have:
- Around 3–5 years of Regulatory Affairs experience within the EU.
- Solid knowledge of EU regulatory framework and procedures.
- A hands-on and proactive mindset – you take ownership and move things forward.
- Ability to work across functions and manage multiple priorities.
- A background that shows versatility (e.g. exposure beyond a narrow RA scope or experience from different types of companies).
What We Offer:
- A role with real ownership and the opportunity to grow in responsibility.
- Close collaboration with senior regulatory leadership as a trusted deputy.
- Exposure to the full regulatory lifecycle and cross-functional projects.
- The opportunity to help build and shape how regulatory is handled internally.
- A dynamic environment where initiative and curiosity are valued.
EU Regulatory Affairs Manager in Farnborough employer: Abacus Medicine Group
Contact Detail:
Abacus Medicine Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land EU Regulatory Affairs Manager in Farnborough
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend relevant events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory processes. Be ready to discuss how your hands-on experience aligns with their needs. Show them you’re not just about execution but also about taking ownership and driving projects forward.
✨Tip Number 3
Practice your pitch! You want to convey your passion for regulatory affairs and how you can contribute to building and improving processes. Keep it concise and engaging – think of it as your personal brand statement.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive and take the initiative to engage with us directly.
We think you need these skills to ace EU Regulatory Affairs Manager in Farnborough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that match the EU Regulatory Affairs role. Highlight your hands-on experience and any projects where you've taken ownership, as this is what we’re looking for!
Craft a Compelling Cover Letter: Use your cover letter to tell us why you’re passionate about regulatory affairs and how your background aligns with our needs. Show us your proactive mindset and curiosity – we love candidates who take initiative!
Showcase Your Versatility: We want to see that you have a broad understanding of the regulatory landscape. Mention any diverse experiences or roles you've had that demonstrate your ability to work across functions and manage multiple priorities.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at Abacus Medicine Group
✨Know Your Regulatory Stuff
Make sure you brush up on the EU regulatory framework and procedures. Be ready to discuss your experience with submissions and lifecycle management, as this will show that you’re not just familiar with the basics but can also handle the complexities of the role.
✨Show Your Hands-On Approach
This role is all about taking ownership, so come prepared with examples of how you've proactively driven projects in the past. Highlight situations where you’ve improved processes or taken initiative, as this will demonstrate your hands-on mindset.
✨Cross-Functional Collaboration is Key
Since the job involves working with various teams like Clinical, CMC, QA, and Commercial, be ready to talk about your experience collaborating across functions. Share specific examples of how you’ve successfully worked with different departments to achieve a common goal.
✨Be Curious and Versatile
The company values curiosity and versatility, so don’t hesitate to showcase your diverse background. Discuss any experiences that go beyond a narrow regulatory scope, as this will illustrate your adaptability and eagerness to learn and grow within the role.