Research and development | GSK

Help us maintain standards to positively impact lives 

Help us make sure our medicines and vaccines are effective, and of a high quality. That is how we can deliver what matters most to our patients across the world. 

We are looking for graduates in Regulatory affairs

Are you an analytical graduate who can help us ensure our medicines meet rigorous legal standards? This will be your challenge within our dedicated regulatory affairs department. It is here that we advise on legal and scientific requirements; collect, collate, and evaluate scientific data in order to confirm the quality and efficacy of our products – and keep track of changing global health authority requirements.

We have to meet stringent standards as part of the registration for clinical trials and marketing approvals across the world. You can be instrumental in this crucial process. Working with different areas of the function, other departments and colleagues from around the world, you will get an unparalleled insight into a critical team and the chance to provide expert guidance. 

Develop your critical skills in a global biopharma company

If you are a graduate with the talent and ambition eager to make an impact on billions of lives, we will help you develop the expertise to become one of our GSK graduates. Over two years, our graduate programme will challenge and support you to grow professionally and personally. You will have stretching rotations supporting areas such as therapeutic, chemistry, manufacturing and control (CMC), labelling or the UK and Ireland business. As you experience these varied fields of expertise, you will learn exactly what it takes to get a drug approved.

With access to first-class support and development opportunities, you will be well-equipped to start your professional career and make a meaningful impact at GSK

Learn more about a career in regulatory affairs. 

No Byline Policy

Editorial Guidelines

Corrections Policy

Source