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
Apr 17, 2026
Full time
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
A pharmaceutical company based in Farnborough is looking for a Deputy in Regulatory Affairs to manage EU regulatory activities. With 3-5 years of experience in Regulatory Affairs, you will support submissions and collaborate across various teams. The role requires a proactive mindset, solid knowledge of EU regulations, and the ability to lead projects. This is a hands-on position with opportunities for growth and development in a dynamic environment where initiative is valued. Apply now to take ownership of regulatory processes.
Apr 17, 2026
Full time
A pharmaceutical company based in Farnborough is looking for a Deputy in Regulatory Affairs to manage EU regulatory activities. With 3-5 years of experience in Regulatory Affairs, you will support submissions and collaborate across various teams. The role requires a proactive mindset, solid knowledge of EU regulations, and the ability to lead projects. This is a hands-on position with opportunities for growth and development in a dynamic environment where initiative is valued. Apply now to take ownership of regulatory processes.