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.
Immerse yourself in the fascinating everyday working life at Roche in Basel, where we modernize technical operations to enable the delivery of medicines to patients more quickly, efficiently, and reliably.
The Pharma Technical Operations (PT) Global MSAT & Engineering (PTT) group takes bold steps to modernize technical operations to enable Roche to deliver medicines for patients more quickly, efficiently and reliably. PTT shapes and accelerates technology innovation and product lifecycle management for tomorrow, while standardizing and driving operational excellence in PT today.
The Pharma Technical Operations Direct Materials Team drives the modernization of materials and their application to technical issues across PT. In partnership with key stakeholders, the team manages the Certifications and Filings for Biologics and Synthetic Molecules, specifically handling content and document management for Direct Materials.
Regulatory Compliance & Filing Strategy: Contribute to the design and execution of global Certification and Filing processes. You will learn to navigate complex Health Authority requirements (such as BSE/TSE, GMO)
Cross-Functional Stakeholder Management: Act as a liaison between key departments including Procurement, Quality Control, Manufacturing, and Regulatory Affairs. You will participate in the authoring and review of technical documents and help maintain a state of "inspection readiness".
Process Design & Systems Integration: Support the ASPIRE program by assisting in the design and implementation of Direct Material Management workflows. This includes gaining hands-on experience in data management and learning how technical specifications translate into global system requirements for Biologics and Synthetic molecules.
Enrolled in or completed a Master's degree or in role PhD in Science, Chemistry, Materials Science, Pharmaceutical Sciences, or an equivalent technical discipline.
You have a proven foundational knowledge of material properties and regulatory principles.
You are a quick learner with an exceptional eye for detail.
You are curious, open minded and solution-focused.
You are fluent in English, German proficiency is a plus
The start date for the internship is March or April 2026, with a duration of 12 months.
Full-time or part-time (at least 80%) employment is possible.
Writing a thesis during this internship is not permitted.
For applicants from outside the EU/EFTA without a residence permit: a mandatory letter from the university is required, including duration, and a valid enrollment certificate.
Ready to take the next step? We'd love to hear from you. Apply now to explore this exciting opportunity!
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.