Regulatory Affairs Graduate - 12 months

Description

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 leading pharmaceutical company, we are committed to innovation, excellence, and making a positive impact on global healthcare. Join us in our mission to shape the future of healthcare and make a difference in the lives of millions.

Why Choose Shionogi?

Shionogi offers a dynamic, collaborative work environment where you can grow your career and contribute to groundbreaking healthcare advancements. We value diversity, inclusion, and the unique perspectives that each team member brings. At Shionogi, you will have the opportunity to work with talented professionals, engage in meaningful projects, and be part of a company that is at the forefront of medical innovation.

About the Role

This graduate programme aims to give the successful applicant first-hand experience and a learning opportunity in European Regulatory Affairs (Strategy, Submission, Operations and Intelligence). Exposure to the Shionogi Regulatory Affairs team will facilitate your understanding of the breadth and importance of regulatory affairs to the success of a pharmaceutical company during drug development and throughout product’s lifecycle.

Working with the Shionogi Regulatory department, you will receive extensive mentorship and training in all aspects of the job and can expect to gain valuable knowledge of regulatory procedures, systems and processes. You will develop essential skills that are relevant for future strategic and operational roles in regulatory affairs or other related disciplines in drug development.

Responsibilities and Duties

1. Collaborate with the European Regulatory Team on various projects and activities.
2. Define project scope, goals, and deliverables, and manage project timelines and milestones.
3. Support the Regulatory Department in achieving internal and external deliverables and compliance.
4. Monitor and interpret changes in regulatory requirements and regulations.
5. Act as the regional point of contact for regulatory information and document management system enhancements.
6. Oversee project timelines for regulatory deliverables and ensure timely completion.
7. Liaise with project stakeholders to track milestones and deliverables.
8. Prepare progress reports and presentations on regulatory topics.

Requirements

1. A university degree or currently enrolled in a life science degree course (i.e., Pharmacy, Biology, Chemistry, Development, or manufacturing of medicinal products).
2. An interest in regulatory affairs and drug development and wanting to learn more.
3. Ability to work collaboratively in a team setting.
4. Ability to communicate effectively in English, both verbally and in writing.
5. Demonstrated you are a high-performance individual with a strong work ethic.

Join Us

If you are driven to make a tangible difference, please apply. Together, we can forge a path to a healthier world.

The application process will close on 18th February .

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