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Location
In office (Basel)
Seniority
Intern
Employment
Internship

Confirmed on the employer's own hiring board on Nov 4, 2026. First seen by Alion on Nov 4, 2026. Roche scores A on the Alion truth index.

Overview
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Roche is a Swiss healthcare group founded in Basel in 1896 and is unusual in operating two large divisions of comparable importance: prescription medicines and in vitro diagnostics. The pharmaceutical business is built on oncology, neurology, immunology, ophthalmology and haemophilia, with products such as Ocrevus, Hemlibra, Perjeta and Vabysmo, while the diagnostics division supplies laboratory analysers, molecular tests and sequencing systems to hospitals worldwide. The group owns the American biotechnology company Genentech outright and the Japanese firm Chugai in majority, is controlled by a family shareholder pool, and spends among the largest research budgets in the industry.

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

The Process Validation Chapter is a part of the Basel Drug Substance Manufacturing organization and is responsible for supporting the validation of the production process during routine commercial manufacturing, technology transfers, process optimizations and for leading implementation of new technologies to drive manufacturing efficiencies.

This internship position is located in Basel, Switzerland.

The Opportunity:

  • You will contribute to process validation strategies, execution, and projects to drive operational success across manufacturing.
  • Supporting technical process technology transfers enables you to play a key role in transitioning processes from development into commercial-scale manufacturing.
  • You will manage end-to-end validation deliverables, spanning conceptual work, plan creation, training implementation, sample coordination, data interpretation, and report preparation.
  • Cross-functional troubleshooting activities will be planned and coordinated by you in close collaboration with pilot laboratories, production, and the quality department.
  • You will process deviations and changes in full compliance with GMP guidelines.
  • Active involvement in optimization projects will allow you to drive continuous improvement, efficiency, and process robustness.

Who You Are:

  • You are currently enrolled in a Bachelor’s or Master’s program, or have completed your degree within the last 12 months prior to the start date, in a scientific or technical field-preferably in Biotechnology, Bioprocess engineering, or (bio)Chemical engineering, Pharmacy, Biology.
  • Practical experience or solid knowledge of working within a regulated GMP environment will be a core foundation of your qualifications.
  • You will bring a collaborative mindset as an independent team player who thrives in a dynamic environment and enjoys partnering across diverse interfaces.
  • Adapting quickly to a fast-paced setting will enable you to manage shifting priorities effectively and respond with agility to operational requests.
  • Strong interpersonal and communication skills will allow you to articulate complex technical topics clearly and build productive working relationships.
  • Fluency in English is required to collaborate and communicate clearly within an international, cross-functional team. Conversational German skills are considered an asset.

Additional Information:

  • Start Date & Duration: The preferred start date for the internship is in early 2027 with a duration of 12 months (or upon mutual agreement).

Application Process:

  • Please upload your CV (in English), a motivation letter with your application, and a certificate of enrollment (if you are currently studying) or your degree certificate (if you have already completed your studies).
  • Non-EU/Non-EFTA citizens must attach an official confirmation from your university stating that a mandatory internship is an integral part of your curriculum, and you must remain continuously enrolled throughout the entire duration of this internship.

Ready to take the next step? We look forward to receiving your application!

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.

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