Intern- Regulatory Affairs
About this opportunity
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
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.
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.
Job details
How this role compares
Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.
We currently track 21 comparable Intern/Fellow/Postdoc Regulatory Affairs roles across 10 biopharma companies.
Salary context
2 of 21 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 21 comparable roles
+ 4 more countries
Seniority mix
21 of 21 peers have a known seniority level
Therapeutic area mix
0 of 21 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.