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Help us get ahead of disease together with our Internship Programme

Education required: You are regularly enrolled in a Master in Regulatory Affairs, Engineering, Pharmacy, Biology, Chemistry, Bioengineering or a related field in an Educational Establishment located in Europe.

Language requirement: You are proficient in English.

Other requirements: You have good interpersonal and communication skills and value honesty and transparency.

Expected start date: As soon as possible.

Duration: 3 to 6 months.

Requisite: The internship must be mandatory & done in the framework of the curriculum, for which an agreement must be signed between GSK, the student and the Educational Establishment.

Remuneration: according to Belgian legal requirements, the internship will not be paid. However, some expenses will be reimbursed.

Application deadline: We will close this vacancy when we have enough applications, so please apply as soon as you can to be considered.

Are you looking to gain valuable world work experience and help to positively impact the health of billions of people? Apply for a GSK Internship today!

A GSK internship offers you the opportunity to kickstart your career – to take on a real role with genuine impact!  You’ll take on challenging, serious work on live projects or assignments.  You’ll also get to learn from us, develop your skills and gain valuable experience for wherever the future takes you.

What will you do?

• You will get tailored on-the-job training from Regulatory Affairs experts and take part in meaningful tasks that support vaccine development and lifecycle management, for example:

• Preparation and authoring of technical regulatory documents for vaccines in compliance with the applicable regulatory & scientific standards.

• Help compile market specific requirements.

• Support the preparation of responses to regulatory authority questions.

• Assist with deployment and adoption of new IT tools (Artificial Intelligence & Digital fluency) for GSK vaccines within Global Regulatory Affairs.

• Contribute to a variety of other regulatory and cross-functional projects

What are we looking for?

• Real responsibility: work on live projects that contribute to public health

• Learn from experts: mentorship and practical training from Regulatory Affairs professionals

• Career boost: gain experience and skills highly valued by future employers

• Make an impact : help bring safe, effective vaccines to patients around the world

Let’s do this!

You’ll find hints, tips and guidance on our recruitment process on our website.

Learn more about the application process gsk.to/ECprocess.

You can learn more about GSK and our careers here https://www.gsk.com/en-gb/careers/

Apply now!

Need help with your application?

Please email us at WW.EarlyCareers@gsk.com and let us know how we can help you.

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If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

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