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At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.<h3></h3><h3>The Position</h3>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.<h3>The Opportunity</h3>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.<h3>During the internship, what will you do: </h3><ul><li>Support regulatory professionals, driving innovative regulatory strategies and produce high-quality CMC dossiers in agile and digital space</li><li>Operate as a member of global, self-managed squad teams, aligning with the organization's agile implementation.</li><li>Gain practical experience by working on various quality-related regulatory activities across the whole development lifecycle from clinical trial applications through to license applications and maintenance</li><li>Contribute to operational and business excellence aspects of regulatory, including document management, data/insights generation and business systems to advance digital and data solutions. </li><li>Work on genuine, impactful projects, providing real added value by assisting teams with their daily tasks and progressively taking ownership of defined individual projects.</li></ul><h3>Benefits for you:</h3>We will provide you with an excellent learning experience in a global matrix organization:<ul><li>Professional Experience - Acquire significant hands-on experience in Technical Regulatory Affairs, including operational activities and the application of digital solutions in the regulatory landscape. </li><li>Regulatory Expertise - Develop a comprehensive understanding of the regulatory requirements for delivering transformative medicines (products and devices) to patients</li><li>Global Insight - Gain cross-functional insight into a global pharma organization and experience collaborating with diverse stakeholders within a matrix environment. </li><li>Personal and Professional Growth - Access learning and training opportunities to improve your personal and professional development</li><li>Cultural Immersion - Become an active member of our Interns’ Network and immerse yourself in the inspiring culture of Basel in the heart of Europe:</li></ul><h3>Your Profile & Qualifications</h3>To be considered for this challenging opportunity, you must meet the following educational requirements:<ul><li>You are currently enrolled in a life sciences or pharmaceutical sciences Master’s (or you have graduated on or after 1 September 2025). If you have graduated, please include your graduation date in your motivation letter or CV.</li></ul><h3>Your qualifications include, but are not limited to, the following:</h3><ul><li>Prior experience or knowledge in regulatory affairs is an advantage</li><li>Ability to drive activities, work under time pressure to deliver within tight timelines</li><li>Good coordination and communication skills</li><li>Strong organizational and analytical skills</li><li>Proficient English language skills</li></ul><h3>Applications requirements</h3><ul><li>Your application must include a CV and a motivation letter that specifically addresses the following three question? Why are you specifically interested in Technical Regulatory Affairs (CMC) at Roche, and how does this internship align with your career goals</li><li>What relevant skills and experience will you bring to this position and provide a specific example of their application?</li><li>""What do you consider the most significant regulatory challenge currently facing a global healthcare company like Roche, and why?"</li></ul>The internship will take place in the Roche Basel office.The start date of the internship is 1 September 2026 for 12 months.We will accept your application until 11:59 pm (CET) on Friday, 10th April 2026.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.Student Internship in Technical Regulatory Affairs (12 Months, Starting September 2026) <h3>Who we are</h3>A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together.Roche is an Equal Opportunity Employer.

Student Internship in Technical Regulatory Affairs (starting in September 2026, 12 Months, in Basel)

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Roche

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