Regulatory Affairs Internship at Roche, Spain | Diagnostics and AI Projects
How do diagnostic products navigate different regulatory requirements around the world—and where can AI help? This Roche Regulatory Affairs Internship offers recent graduates experience in global product registrations, regulatory documentation, and AI-supported workflows. Based in Sant Cugat del Vallès, Barcelona, Spain, the 12-month opportunity combines diagnostics regulation with practical technology projects.
- Position: Regulatory Affairs Intern
- Location: Sant Cugat del Vallès, Barcelona, Spain
- Job ID: 202610-127493
- Team: Global Regulatory Affairs
- Category: Vocational & Development Programs
About The Company
Roche develops medicines and diagnostic products to advance healthcare. This position supports Roche Diagnostics, working with international teams involved in product development, regulatory activities, and lifecycle management.
Roche Regulatory Affairs Internship Description
The intern will support regulatory and product care activities for in vitro diagnostic (IVD) and medical device (MD) products. Following onboarding, assignments will provide insight into applicable regulations, industry standards, and different stages of the product lifecycle.
The Roche Regulatory Affairs Internship also includes projects using AI tools to improve regulatory tracking, document analysis, and reporting within a regulated environment.
Key Responsibilities
- Assist with worldwide registrations and regulatory activities for IVD/MD products across their development and lifecycle.
- Support the preparation and maintenance of global product documentation.
- Collaborate with regulatory teams and local affiliates on registration activities.
- Coordinate with interdisciplinary teams on regulatory input, submission planning, and documentation.
- Support non-registration activities within Global Regulatory Affairs.
- Assist with designing, developing, and testing AI-powered tools and dashboards for regulatory tracking, document analysis, and automated reporting.
- Participate in training and fine-tuning AI tools for regulatory applications, supporting accuracy and compliance with internal standards.
- Follow emerging AI technologies and changes in relevant healthcare and pharmaceutical regulatory guidance.
Educational Requirements and Eligibility
- Graduated within the last three years in Biology, Life Sciences, Engineering, or Data Science.
- Fluent in written and spoken English.
- Familiarity with AI tools and prompt engineering.
Skills and Qualifications
- Strong facilitation and communication skills.
- Ability to handle challenges within a multicultural, international environment.
- A proactive approach to learning and finding solutions.
- Strong teamwork and collaboration.
- Curiosity, attention to detail, and problem-solving abilities.
Learning and Development
The internship offers mentoring, exposure to end-to-end diagnostic and medical device development, and opportunities to build regulatory knowledge. Participants will also gain experience applying AI in a regulated setting, with flexible working arrangements and cross-functional networking.
Roche Regulatory Affairs Internship Application Details
- Duration: 12 months.
- Working Arrangement: Flexibility is mentioned, but specific onsite or remote expectations are not provided.
Interested in connecting your scientific background with regulatory strategy and technology? This Roche Regulatory Affairs Internship offers experience in diagnostic product registrations, global documentation, and AI-supported projects. If you graduated within the last three years and meet the requirements, consider applying for the Barcelona opportunity.
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