Regulatory Affairs Policy and Intelligence Graduate (12-month contract)
Start Your Career in European Regulatory Affairs with Shionogi
Shape the Future of Healthcare with Shionogi
At Shionogi, we are dedicated to improving the health and well-being of people around the world. As a research-driven pharmaceutical company, we are committed to innovation, scientific excellence, and making a meaningful difference for patients globally.
Shionogi offers a collaborative, inclusive, and forward-thinking environment where early-career professionals can learn, grow, and build a strong foundation for a career in the pharmaceutical industry.
About the Role
We are offering an exciting opportunity for a Regulatory Affairs Graduate to join our European Regulatory Affairs team, with a primary focus on Regulatory Policy & Intelligence. This is a hands-on role, working closely with experienced regulatory professionals to gather, analyse, and provide accurate and timely regulatory information to the wider Regulatory Affairs team.
The role will provide practical experience, structured learning, and close mentorship, giving you exposure to the breadth of European Regulatory Affairs and its critical role across the full product lifecycle.
Key Responsibilities:
- Support the monitoring, assessment, and dissemination of European legislation and regulatory requirements
- Assist with gathering and analysing regulatory intelligence on competitor products in several therapeutic areas (Infectious Diseases, Neurosciences, Metabolism…)
- Contribute to the maintenance of digital and IT solutions supporting regulatory intelligence
- Support preparation of position papers on selected Policy priorities and responses to draft legislation
- Collaborate with European Regulatory Affairs teams on product development and portfolio activities
What We Are Looking For
We are looking for a motivated and curious graduate who is keen to build a career in Regulatory Affairs and develop a strong understanding of the European regulatory environment within a pharmaceutical company.
You will bring:
- An advanced scientific academic background in a relevant discipline such as Pharmacy, Biochemistry, Biopharmaceutical development or a related pharma/life science. General knowledge of diseases and drug development is desired.
- A genuine interest in regulatory affairs, pharma R&D, policy making and healthcare, with a desire to understand how regulation supports patient access to medicines
- Strong analytical skills, with the ability to review regulatory information, identify key points, and communicate these clearly to relevant R&D functions
- Excellent attention to detail, with a structured and methodical approach to handling data, documentation, and regulatory information. Interest in AI/ML/LLM and use of agents/bots is a plus.
- Good written and verbal communication skills in English, with confidence working with colleagues across different functions and geographies. An additional EU language is a plus.
- The ability to work collaboratively in a team environment, while also managing tasks independently and taking ownership of assigned activities
- A proactive mindset, with the confidence to ask questions, seek learning opportunities, and continuously develop new skills
Join Us
If you are curious, driven, and excited about contributing to the development and availability of medicines that improve patients’ lives, we would love to hear from you.
Apply now and take the first step in shaping the future of healthcare with Shionogi.
The closing date for applications is 30th March 2026.
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Start Your Career in European Regulatory Affairs with Shionogi
Shape the Future of Healthcare with Shionogi
At Shionogi, we are dedicated to improving the health and well-being of people around the world. As a research-driven pharmaceutical company, we are committed to innovation, scientific excellence, and making a meaningful difference for patients globally.
Shionogi offers a collaborative, inclusive, and forward-thinking environment where early-career professionals can learn, grow, and build a strong foundation for a career in the pharmaceutical industry.
About the Role
We are offering an exciting opportunity for a Regulatory Affairs Graduate to join our European Regulatory Affairs team, with a primary focus on Regulatory Policy & Intelligence. This is a hands-on role, working closely with experienced regulatory professionals to gather, analyse, and provide accurate and timely regulatory information to the wider Regulatory Affairs team.
The role will provide practical experience, structured learning, and close mentorship, giving you exposure to the breadth of European Regulatory Affairs and its critical role across the full product lifecycle.
Key Responsibilities:
- Support the monitoring, assessment, and dissemination of European legislation and regulatory requirements
- Assist with gathering and analysing regulatory intelligence on competitor products in several therapeutic areas (Infectious Diseases, Neurosciences, Metabolism…)
- Contribute to the maintenance of digital and IT solutions supporting regulatory intelligence
- Support preparation of position papers on selected Policy priorities and responses to draft legislation
- Collaborate with European Regulatory Affairs teams on product development and portfolio activities
What We Are Looking For
We are looking for a motivated and curious graduate who is keen to build a career in Regulatory Affairs and develop a strong understanding of the European regulatory environment within a pharmaceutical company.
You will bring:
- An advanced scientific academic background in a relevant discipline such as Pharmacy, Biochemistry, Biopharmaceutical development or a related pharma/life science. General knowledge of diseases and drug development is desired.
- A genuine interest in regulatory affairs, pharma R&D, policy making and healthcare, with a desire to understand how regulation supports patient access to medicines
- Strong analytical skills, with the ability to review regulatory information, identify key points, and communicate these clearly to relevant R&D functions
- Excellent attention to detail, with a structured and methodical approach to handling data, documentation, and regulatory information. Interest in AI/ML/LLM and use of agents/bots is a plus.
- Good written and verbal communication skills in English, with confidence working with colleagues across different functions and geographies. An additional EU language is a plus.
- The ability to work collaboratively in a team environment, while also managing tasks independently and taking ownership of assigned activities
- A proactive mindset, with the confidence to ask questions, seek learning opportunities, and continuously develop new skills
Join Us
If you are curious, driven, and excited about contributing to the development and availability of medicines that improve patients’ lives, we would love to hear from you.
Apply now and take the first step in shaping the future of healthcare with Shionogi.
The closing date for applications is 30th March 2026.
