EU Regulatory Affairs Manager

The opportunity

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

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