Hybrid EU Regulatory Affairs Manager

Posted 20 minutes ago

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About the role

  • 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

Job title

EU Regulatory Affairs Manager

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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