Regulatory Affairs Intern
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
The role:
We are looking for 1 intern who wants to be part of our Medical Affairs & License to Operate chapter in the regulatory affairs department. The Regulatory Affairs intern performs the coordination and preparation of document packages for regulatory submissions to ensure alignment and compliance with local and regional registration requirements as well as with company policies, SOPs, internal audits, and inspections. Compiles all materials required in submissions, license renewal, and annual registrations.
Your main responsibilities:
Analyze and communicate internal and external regulatory intelligence
Provide regulatory input into cross-functional Affiliate business meeting
Filing: Adapt global product dossiers to local requirements, prepare and manage regulatory registration filings across product life cycles, monitor and communicate all regulatory filing status
Perform affiliate regulatory activities on relevant Roche systems
Ensure regulatory inspection-readiness for the Affiliate
Ensure regulatory compliance for products released to market according to marketing authorizations
Review promotional and non-promotional material
Who are we looking for?
You, as an ideal candidate, will have the following experience, education, and knowledge:
Recent graduate with no more than 2 years of experience
University Degree in Pharmacy / Medicine or other relevant Pharmaceutical or Biological Disciplines.
Pharm D preferred
You, as an ideal candidate, will have the following skills:
Fluence in French
Basic knowledge of English (written & spoken) with clear commitment on improving your language skills
Eager to learn, self-managed & directed, bold, and being able to prioritize
The ability to work with cross-functional teams is a must
Ability to understand and leverage digital means and tools
Ability to deeply listen, question & understand, and communicate smoothly
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.