Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.

The Position

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.

Creating a world where we all have more time with the people we love.

That’s what makes us Roche.

The Opportunity

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 regulatory professionals, driving innovative regulatory strategies and produce high-quality CMC dossiers in agile and digital space

Be part of a global  self-managed teams as per the agile concepts implemented throughout the organization

Get hands-on experience by working on various quality-related regulatory activities across the whole development value chain from clinical trial applications through to license applications and maintenance

Contribute to operational and business excellence aspects of regulatory, including document management, data/insights generation and business systems to support the organization effort into digital solutions. 

The projects you will work on are real, and you will be generating genuine added value ,  by supporting teams in their daily tasks and gradually assume responsibility for agreed individual projects

Benefits for you:

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

Acquire meaningful professional experience in the field of Technical Regulatory Affairs and operation activities, including digital solutions in the regulatory landscape. 

Develop a deep understanding of the regulatory requirements for delivering transformative medicines (products and devices) to patients

Gain cross-functional insight into a global pharma organization and experience working in matrix environment, collaborating with stakeholders 

Access learning and training opportunities to improve your personal and professional development

Become a member of our Interns’ Network and immerse yourself in the inspiring culture of Basel in the heart of Europe

Who You Are

To seek this challenging opportunity, you are currently enrolled in a life sciences or pharmaceutical sciences Master’s (or you have graduated on or after 1 September 2024). If you have graduated, please include your graduation date in your motivation letter or CV.

Your qualifications include, but are not limited to, the following:

Previous experience or knowledge in regulatory affairs is an advantage

Ability to drive activities, work under time pressure to deliver within  tight timelines

Good coordination and communication skills

Strong organizational and analytical skills

Proficient English language skills

Applications need to include a CV and a motivation letter answering these 3 questions:

Why do you want to do an internship in Technical Regulatory Affairs at Roche Basel?

What relevant skills and experience will you bring to this position?

What challenges do you see in the field of Technical Regulatory Affairs?

The internship will take place in the Roche Basel office.

The start date of the internship is 1 September 2025 for 12 months.

Due to regulations, non-EU/non-EFTA citizens need to provide a certificate of enrolment, as well as a certificate from the university stating that the internship is mandatory and stating the length of it. This restriction does not apply for non-EU/non-EFTA citizens with a family reunion B-Permit with working allowance, C-Permit or S-Permit.

What do we stand for? Roche embraces diversity and equal opportunity in a serious way. We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.

Who we are

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10,700 employees from over 100 countries come together at our Basel/Kaiseraugst site, which is one of Roche`s largest sites. Read more.

Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees also benefit from multiple services on site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events.

We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche.

Roche is an Equal Opportunity Employer.