Student Internship in Technical Regulatory Affairs (starting in September, 6-12 Months) in Basel

At Roche, we believe it’s urgent to deliver medical solutions right now—even as we develop innovations for the future. We are passionate about transforming patients’ lives and we are fearless in both decision and action. And we believe that good business means a better world.

That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow.

As an Intern within our team in Basel, you will gain insight into the work of Technical Regulatory Affairs professionals who are responsible for providing the regulatory input and leadership for quality-related aspects of pharmaceuticals. The activities span the whole lifecycle of the product, from clinical trials all the way to the maintenance of products at the end of their lifecycle.

During the internship you will:

• Support Technical Regulatory Managers in their daily tasks and gradually assume responsibility for agreed individual projects
• Get hands on experience by working on various quality-related regulatory activities from clinical trial applications through to license applications and maintenance
• The project you will work on is real and you will be generating genuine added value

Benefits for you:

We will provide you with an excellent learning experience in a dynamic global organization:

• Gain meaningful professional experience in the field of Technical Regulatory Affairs.
• Develop an understanding of the regulatory requirements for bringing medicines to patients.
• Gain cross-functional insight into a global research organization and learn how to work in a global company, to network and to collaborate with stakeholder groups.
• Be given learning and training opportunities to improve your personal development.
• Be a member of our Interns’ Network and experience the culture of Basel in the heart of Europe.

Who You Are

To take on this challenging opportunity you are enrolled in a Master’s or Ph.D. program in life sciences or pharmaceutical sciences and nearing the end of your studies. Your qualifications include, but are not limited to, the following:

• Passionate about the field of Technical Regulatory Affairs
• First regulatory experience is a plus
• Ability to drive activities, work under pressure and to tight timelines
• Good coordination and excellent communication skills
• Strong organizational and analytical skills
• Outstanding motivation and willingness to learn
• Excellent English language skills

Applications need to include a CV, a motivation letter and your answer to these 3 questions:

• Why do you want to do an internship in Technical Regulatory Affairs?
• What relevant skills and experience will you bring to this position?
• What challenges do you see in the field of Technical Regulatory Affairs?

The preferred start date of the internship is beginning of September 2019.

Due to regulations non-EU/EFTA citizens have to provide a certificate from the university stating that an internship is mandatory as part of the application documents.