Internship as GMP Excellence Engineer in the field of Clinical Packaging (Kaiseraugst, 12 months)

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.
The Position
As part of Pharma Technical Development (PTD), we realize our pharma ambitions: We bring groundbreaking therapies from clinical Phase I to market maturity in order to provide reliable supply to every patient every day. The group works closely with external and internal interfaces, the Compliance Team, and Quality Assurance. It is crucial for ensuring smooth operations and the reliable supply of primary and secondary packaging for clinical trials.
The Opportunity
Are you ready to make a decisive contribution to pharmaceutical development and gain profound insights into the world of clinical packaging? Are you looking for a challenging and at the same time highly relevant internship position where you can actively participate in the design and optimization of processes?
Then we have exactly the right thing for you. We offer a unique internship opportunity in our clinical packaging area at the Kaiseraugst location. Here you will work at the interface of technology, quality, and patient safety.
As an intern in GMP document management, you will take on a central role in structuring, harmonizing, and revising our existing GMP documents. This is an essential building block for the quality, compliance, and efficiency of our clinical packaging processes. Your mission: bring structure to the GMP document landscape. Your main tasks include:
Analysis and evaluation of existing GMP documents (SOPs, technical documents, master validation plans, validation plans, operating instructions, etc.) for completeness, consistency, and currency.
Structuring and harmonizing the document landscape to minimize redundancies and create a clear, uniform system.
Revision and redrafting of documents in close cooperation with subject matter experts to ensure they meet current regulatory requirements and internal standards.
Active participation in the implementation of document management systems and processes.
Support in the preparation and execution of audits and inspections from a documentation perspective.
This internship offers you a rare opportunity to get to know a wide spectrum of pharmaceutical packaging. You will not only gain deep insights into the clinical supply chain and the specific requirements for clinical trial materials, but also into the strict GMP guidelines that shape our industry.
You will work in a dynamic team dedicated to providing vital medicines for clinical trials worldwide. You will learn from experienced engineers, quality managers, and operations experts and contribute directly to ensuring that our processes run smoothly and compliantly.
Who You Are
You are a student in the field of pharmaceutical technology, engineering (e.g., mechanical engineering, process engineering), natural sciences, or a comparable course of study, or you have already successfully completed your studies and are looking for professional experience. Furthermore, you have:
a strong interest in quality assurance, regulatory requirements (GMP), and document management.
Proficiency in MS Office (especially Word, Excel, PowerPoint) is a matter of course for you.
You are fluent in German and English (oral and written).
You work extremely structured, precise, and detail-oriented.
You possess very good analytical skills and the ability to formulate complex issues clearly and understandably.
You are motivated, independent, and proactive.
You are looking for a pure internship to gain valuable professional experience.
Additional Information
The internship is for a duration of 12 months.
The earliest start date is 1 December 2026.
Supervision of a Bachelor's or Master's thesis is not possible in this position.
We look forward to your meaningful application with CV, cover letter, and certificates.
Non-EU/EFTA citizens (m/f/d) must attach a confirmation from the university to the application stating that they must complete a mandatory internship as part of their studies.
Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity!
Who we are
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.