Regulatory Affairs Internship at Roche in Switzerland
Step into the world of pharmaceutical innovation with a Regulatory Affairs Internship at Roche in Basel, Switzerland. This Student Internship offers a 12-month, hands-on experience where life science graduates can gain practical insights into technical regulatory affairs, CMC dossier preparation, and agile regulatory strategies. Perfect for those looking to combine global exposure with impactful regulatory work, this internship is an unparalleled internship opportunity for life science graduates.
About the Company
Roche is a leading global healthcare company dedicated to advancing science and delivering transformative medicines and diagnostics. With over 100,000 employees worldwide, Roche empowers its workforce to innovate, collaborate, and make a global impact. Roche Careers provides interns with the opportunity to gain meaningful experience and contribute to life-changing healthcare solutions.
Internship Details:
- Internship Title: Student Internship in Technical Regulatory Affairs (Starting September 2026, 12 Months, in Basel)
- Location: Basel, Basel-City, Switzerland
- Category: Vocational & Development Programs
- Job ID: 202603-107794
- Start date: 1 September 2026
- Duration: 12 months
- Application deadline: 11:59 pm (CET) on Friday, 10 April 2026
The Regulatory Affairs Intern Position
The organization is driven by the vision of creating a healthier future through continuous innovation and advancement in science, ensuring access to healthcare for all.
The Opportunity
As an Intern within the team in Basel, the candidate will gain insight into the work of Technical Regulatory Affairs professionals. These professionals provide regulatory input and leadership for quality-related aspects of pharmaceuticals across the entire product lifecycle, from clinical trials to product maintenance.
Key Responsibilities:
- Support regulatory professionals by driving innovative regulatory strategies and producing high-quality CMC dossiers in an agile and digital environment.
- Operate as a member of global, self-managed squad teams, aligning with the organization’s agile implementation.
- Gain practical experience in quality-related regulatory activities across the development lifecycle, from clinical trial applications to license applications and maintenance.
- Contribute to operational and business excellence aspects, including document management, data and insights generation, and business systems to advance digital and data solutions.
- Work on impactful projects, assisting teams with daily tasks and progressively taking ownership of defined individual projects.
Profile & Qualifications
Candidates must meet the following educational requirements:
- Currently enrolled in a life sciences or pharmaceutical sciences Master’s program, or graduated on or after 1 September 2025 (graduation date must be included in the application).
Additional Qualifications:
- Prior experience or knowledge in regulatory affairs is advantageous.
- Ability to drive activities and work under time pressure to meet tight timelines.
- Strong coordination and communication skills.
- Strong organizational and analytical skills.
- Proficiency in English.
Application Requirements
Applications must include a CV and a motivation letter addressing the following questions:
- Why is the candidate specifically interested in Technical Regulatory Affairs (CMC) at Roche, and how does the internship align with their career goals?
- What relevant skills and experience will the candidate bring, including a specific example of their application?
- What does the candidate consider the most significant regulatory challenge currently facing a global healthcare company like Roche, and why?
Benefits of Regulatory Affairs Internship
The internship provides an excellent learning experience in a global matrix organization:
- Professional Experience: Hands-on experience in Technical Regulatory Affairs, including operational activities and application of digital solutions.
- Regulatory Expertise: Comprehensive understanding of regulatory requirements for delivering transformative medicines and devices.
- Global Insight: Cross-functional exposure within a global pharmaceutical organization and collaboration with diverse stakeholders.
- Personal and Professional Growth: Access to learning and training opportunities for development.
- Cultural Immersion: Participation in the Interns’ Network and immersion in the culture of Basel, located in the heart of Europe.
