Regulatory Affairs Manager

Regulatory Affairs/Clinical Affairs London, United Kingdom Braunton, North Devon


Description

This is a great opportunity to join a successful and growing global Pharmaceutical organisation and help build the future of a diverse Regulatory Affairs function.  This medicines-focused Regulatory Affairs Manager role within our Global Regulatory Operations Team is intended to support the business in specialist technical projects.

To be successful in this role you will need to be able to demonstrate in-depth CMC knowledge plus a strong technical knowledge of medicinal products, be able to demonstrate knowledge of European Regulatory requirements and be able to apply this in a practical and creative way. Experience of preparing complex variation packages and responses to Health Authority requests is essential, along with proven project management skills and the ability to deal with a number of internal and external stake-holders. Established line management ability and leadership qualities are desired. 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.  We can support with relocation for this role.

We're proud to be an equal opportunity employer- and celebrate our employees' differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status. Different makes us better.