# Regulatory Affairs Intern at Roche

Roche is hiring a Regulatory Affairs Intern. Level rates it Little AI ●○○○; you can [apply on Roche](https://jobsbylevel.com/go/00ea0fc4-c9e4-49a6-a7be-3ad5007731bd?utm_medium=ai-agent).

AI Level 1, AI centrality 27 out of 100. Sant Cugat del Vallès.

## Details

- Company: [Roche](https://jobsbylevel.com/companies/roche)
- AI level: AI Level 1 (score 27 out of 100)
- Location: Sant Cugat del Vallès
- Posted: October 26, 2026
- Apply: https://jobsbylevel.com/go/00ea0fc4-c9e4-49a6-a7be-3ad5007731bd?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=regulatory-affairs-intern-at-roche-bf988e

## Prepare for this job

The job page lists 2 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/regulatory-affairs-intern-at-roche-bf988e

## Description

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 We are looking for a creative, innovative and open-minded intern to join the Global Regulatory Affairs team. As an Intern in Regulatory Affairs, you have the opportunity to support regulatory and product care activities, and get insights into the IVD/MD industry and the applicable regulations and standards for IVD/MD products. In Global Regulatory Affairs we work on specific challenges as a team within all areas of the diagnostic business around the globe, to grow together and to bring the best products to patients while building together a work environment that fits our life. As AI plays an increasing role in our daily lives we are also looking for colleagues who are keen in taking part in high-impact projects that leverage AI Tools to optimize how we navigate the complex landscape of global health regulations. In this intern role, you can clearly demonstrate your creativity and leave a footprint in our products’ lifecycle. You will directly contribute to Roche Diagnostics' vision: innovating diagnostics, shaping healthcare & changing lives. Your key responsibilities: After your onboarding program, you will be assigned to tasks or projects. You’ll be mostly spending your time in: Assisting in the worldwide registrations and activities for various IVD/MD products, at various stages of their development and lifecycle Supporting the preparation and maintenance of global documentation for our IVD/MD products Collaborating with other regulatory affairs teams, including local affiliates, for registrational activities Coordinating with global interdisciplinary project teams to provide regulatory input to development, submission planning, and documentation needed Supporting the global regulatory affairs team members in their non-registrational activities Assisting in the design, development, and testing of AI-powered tools and dashboards for regulatory tracking, document analysis, and automated reporting. Participating in the training and fine-tuning of AI Tools tailored for regulatory use cases, ensuring high accuracy and compliance with internal standards. Keep abreast of emerging AI technologies and changing regulatory guidelines regarding AI in the healthcare and pharmaceutical industries. Who you are: You have recently graduated (within the last 3 years) in the field of Biology, Life Sciences, Engineering or Data Science You are fluent in English (written and spoken) You possess facilitation and communications skills and the ability to deal with adversity in a multicultural and international environment You are a fast learner, have a proactive attitude to drive solutions, and have a high level of team orientation You are curious and attentive to detail with a strong problem-solving capability You have Familiarity with AI tools and prompt engineering What do we offer? Immerse yourself in the dynamic environment of the world’s leading biotech company, gaining hands-on experience with cutting-edge industry practices and shaping the future of global healthcare. Become a Regulatory Affairs professional for IVDs/MDs. Develop a Regulatory Mindset and understand the most important regulations and industry standards. Obtain a unique view of end-to-end IVD/MD development and other functions involved. Exposure to other functions and networks within the organization. Gain experience in a fast-paced, technological and international environment. Lots of learning and a great team to mentor and guide you. Hands-on experience with real-world AI applications in a highly regulated

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/regulatory-affairs-intern-at-roche-bf988e

Source: https://jobsbylevel.com/jobs/regulatory-affairs-intern-at-roche-bf988e

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Level. https://jobsbylevel.com/jobs/regulatory-affairs-intern-at-roche-bf988e.

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