Regulatory Affairs Associate
Due to the growth of the Perrigo business this is a great new opportunity to join a successful and growing global Pharmaceutical organisation and be part of the future of a diverse and further expanding Regulatory Affairs function.
These medicines-focused Senior Regulatory Affairs Associate roles, all based at our Barnsley office in South Yorkshire, are intended to support our ambitious and robust UK and Ireland business expansion plans over the next 3-5 years.
To be successful in these roles you will need to have:
A current awareness of the existing legal framework and forthcoming legislation for medicines in the UK and Ireland.
preferably with a focus on OTC medicines or ‘private-label’ products.
apply knowledge in a practical and creative way
demonstrate excellent planning abilities
effective negotiation skills
strategic thinking and being able to deal with a multitude of internal and external stakeholders.
Experience of submitting new MA applications and variations is essential as is the ability to create new regulatory submission documentation
Knowledge and experience of working with medicinal product labelling would also be an advantage.
As Regulatory Affairs Associate, you will use your hands-on regulatory expertise to contribute to delivering new marketing authorisations and to update existing authorisations to meet the business needs, working closely with the functional leadership and other internal departments as well as with external agencies, partner companies and subject matter experts.
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.