Regulatory Affairs Associate - Medicines

Regulatory Affairs/Clinical Affairs London, United Kingdom


An exciting opportunity work on one of Perrigo's established 'explode' product categories in UK and Ireland.  In this role, you will be working with the UK & Ireland Category leads to ensure delivery of all projects under the assigned portfolio. This will mean Hands-on delivery of Growth and life-cycle projects.

What is key in this role is that you have a ‘give it a go’ attitude, keen attention to detail, and the ability to work on several parallel projects.

Our ideal candidate:

  • A problem solver who likes the challenge of working with multiple priorities, who has a keen interest in the commercial side of being a regulator
  • ideally someone with 1-2 years in reg affairs EU or UKIE (medicines).Experience in publishing will be an advantage

At Perrigo, we believe happy, healthy and safe employees are more engaged and more productive employees; therefore, we view our people as a critical investment. By offering competitive wages and benefits, world-class safety programs, preventative wellness programs and wide variety of development initiatives, we strive to ensure that our employees, and the culture they live in, remain as high quality as they always have been.

Given the continued presence of COVID-19 (coronavirus), all interviews will be conducted by phone or virtual connection to protect our candidates and employees.

We are seeking a diverse applicant pool to ensure the diversity of our team reflects the end consumers we serve through our self-care mission. We are proud to be an equal opportunity employer that celebrates our team’s differences. Individuals of all races, ethnicities, nationalities, ancestries, religious creeds, sexual orientations, genders, gender identities and gender expressions, national origins, ages, mental and physical abilities, familial status,’ veterans status’, military status’ and more are encouraged to apply. TOGETHER, we make lives better.