Intern- Regulatory Affairs

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.

About Roche Diagnostics

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.

That’s what makes us Roche.

Roles

We are seeking an organized, meticulous and problem-solving skills individual to join the

Quality & Regulatory team at Roche Diagnostics. Successful applicants will assist in aspects of product registration change notifications and managing and optimizing our internal tracking databases, ensuring accurate and accessible data for all stakeholders.

This internship is your gateway to understanding Quality and Regulatory compliance within the medical device industry at a global leader like Roche. You will work directly with our internal tools and resources, building the kind of real-world experience that truly helps your resume stand out. Join us to develop your skills alongside experts and discover how we shape a healthier future.

Responsibilities

● Assist with preparing and submitting product registration updates to secure

approvals across our portfolio.

● Monitor, collect, and synthesize regulatory updates from official government

portals and industry sources.

● Learn and leverage internal digital tools to automate manual processes and

optimize team efficiency.

● Manage internal tracking databases to maintain high data integrity and accuracy.

● Communicate and collaborate with cross-functional partners, including local,

regional, and global stakeholders on regulatory and quality related projects.

● Support special Q&R tasks as needed.

Qualifications & Skills

● Currently pursuing a Degree in Biomedical Science, Pharmacy, Biomedical

Engineering, Life Sciences, or a related field, with a genuine curiosity about

medical device regulations and how they shape healthcare innovation.

● Exceptionally meticulous with a high sense of responsibility and personal

ownership over data accuracy, tracking databases, and regulatory compliance.

● A fast learner who takes initiative, manages time effectively, and thrives when

working independently with minimal supervision.

● Highly comfortable with technology, with a natural ability to quickly adapt to new software, internal digital tools, and workflow automation systems.

● Excellent verbal and written communication skills paired with an enthusiastic,

proactive attitude—able to collaborate seamlessly across local, regional, and

global cross-functional teams.

Prefer

● Able to commit for 4 to 6 months internship duration

● Please state your exact available commitment dates clearly at the top of your

resume.

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.