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.
Our team is part of a newly assembled central GMP-Support Organization (Operations Support & Compliance, PTDC-T) at the Basel location. With state-of-the-art tools, including AI-supported software systems, we ensure the reliable and efficient flow of all GMP and related business processes. Our responsibilities include areas such as the Quality Management System (QMS), Quality Risk Management (QRM), training, document management, data trending, and inspection management.
The support of our team focuses on the Drug Product Clinical Supply Center in Basel (DP CSC (Parenterals) BS), where sterile dosage forms are manufactured and filled. In addition to the rare opportunity to accompany this operation during the restart of production activities and the associated inspections, the internship also offers a special opportunity to witness the merging of the GMP-Support Organization and the associated process harmonizations and optimizations.
Start of internship: March 2026
Duration: 6-12 months
Location: Basel
The position is not suitable for writing a thesis.
The application requirement for non-EU/EFTA citizens is that the study takes place at a Swiss educational institution.
Have we piqued your interest? Then please upload your resume and a compelling cover letter, as well as the mandatory letter and your enrollment certificate.
Please indicate the possible start and end dates for your internship in your cover letter.
Apply now – we are looking forward to it!