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
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