This is a great opportunity to join a successful and growing global Pharmaceutical organisation and help shape the future of a diverse Regulatory Affairs function.
These medicines-focused Senior Associate Regulatory Affairs roles within our Global Regulatory Operations Team are intended to support the business in specialist technical projects.
The roles are based in a stunning rural setting at our Braunton office in North Devon.
To be successful in these roles you will need to be able to demonstrate CMC knowledge plus a strong technical knowledge of medicinal products, have awareness of European Regulatory requirements and how to apply this knowledge in a practical and creative way. Experience of preparing variation packages and responses to Health Authority requests is essential along with project management skills and the ability to deal with a number of internal and external stake-holders. Knowledge of formulation development, analytical/laboratory experience and/or previous experience of manufacturing site transfers would also be an advantage.
You will provide technical regulatory expertise to multi-disciplinary teams working closely with internal and external manufacturing sites and other internal departments on complex technical projects to ensure delivery to meet the business needs.
At Perrigo we don’t just create jobs we create careers and give you the tools and support to enhance your career development. These are fantastic roles that will give you the chance to develop skills in executing complex regulatory projects.
We can support with relocation for this role.