EU Regulatory Affairs Manager overseeing regulatory activities across assigned products in pharmaceuticals. Ensuring compliance and collaboration within a dynamic team environment in Farnborough.
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
Requirements
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
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