Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Drive EU regulatory projects and improve processes across the full regulatory lifecycle.
- Company: Dynamic pharma company focused on innovation and collaboration.
- Benefits: Ownership of projects, growth opportunities, and close collaboration with senior leaders.
- Other info: Valuable exposure to diverse projects in a fast-paced environment.
- Why this job: Shape the future of regulatory affairs while making a real impact.
- Qualifications: 3-5 years in Regulatory Affairs with a proactive mindset and cross-functional experience.
The predicted salary is between 55000 - 65000 £ per year.
The opportunity is 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. 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.
Responsibilities
- Support and execute EU regulatory activities across assigned products
- Act as internal owner towards 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
Qualifications
- 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)
Benefits
- 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
Contact Detail:
ABACUS MEDICINE 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 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 regulatory frameworks and procedures. We recommend practising common interview questions and scenarios related to regulatory affairs to show you’re ready to take ownership.
✨Tip Number 3
Showcase your versatility! When discussing your experience, highlight projects where you collaborated cross-functionally. We want to see how you’ve worked with different teams and driven initiatives forward.
✨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 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 took ownership, as this is what we’re looking for!
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 proactive mindset can contribute to our team. Don’t forget to mention your experience with EU procedures!
Showcase Cross-Functional Collaboration: We value teamwork here at StudySmarter, so be sure to highlight any experiences where you’ve worked with different teams like Clinical, CMC, or QA. This will show us you can thrive in a collaborative environment.
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 don’t miss out on any important updates during the process!
How to prepare for a job interview at ABACUS MEDICINE
✨Know Your Regulatory Stuff
Make sure you brush up on the EU regulatory framework and procedures. Be ready to discuss specific examples from your past experience that demonstrate your knowledge and how you've applied it in real-world scenarios.
✨Show Your Proactive Side
This role is all about taking ownership, so come prepared with examples of how you've driven projects forward in previous positions. Highlight any initiatives you've taken to improve processes or collaborate across functions.
✨Cross-Functional Collaboration
Since you'll be working with various teams like Clinical, CMC, QA, and Commercial, think of instances where you've successfully collaborated with different departments. Be ready to explain how you navigated challenges and achieved common goals.
✨Ask Insightful Questions
Prepare thoughtful questions that show your interest in the role and the company. Inquire about their current regulatory challenges or how they envision the future of their regulatory processes. This will demonstrate your curiosity and engagement.