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
We are excited to announce the Regulatory Affairs Internship Program, designed to give fresh graduates a comprehensive understanding of regulatory requirements within the pharmaceutical industry. This program offers hands-on experience, engagement in essential regulatory activities, and insights into regulatory frameworks that impact the sector.
As an intern, you will contribute to achieving operational excellence by providing support in the oversight and monitoring of regulatory activities, ensuring compliance with both local regulations and global standards through close collaboration with key stakeholders. You will assist in maintaining regulatory operations, ensuring compliance for Roche medicinal products and medical devices throughout their lifecycle, and enabling the company’s continued license to operate.
Duration: 6 Months
Key Responsibilities:
Execute day-to-day regulatory operations to ensure regulatory compliance of Roche products and medical devices.
Collaborate with local Health Authorities (HAs) and internal stakeholders to build trusted partnerships and effectively manage regulatory operations.
Support the development and maintenance of local product information and country-specific packaging compliant with local and global regulatory standards.
Maintain and oversee all Roche regulatory platforms/systems to ensure alignment with compliance matrices and continuously monitor and improve tracking/control systems.
Participate in the monitoring, preparation, and negotiation of regulatory submissions and responses as part of regulatory lifecycle management.
Who You Are:
A recent graduate with a degree in Pharmacy, Life Science or a related field.
Passionate and genuinely interested in pursuing a career in Regulatory Affairs.
Possess excellent written and verbal communication skills in English.
Demonstrate strong analytical and problem-solving abilities.
Detail-oriented with the ability to work independently and manage multiple tasks effectively.
Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
Behavioral Competencies:
Demonstrate high ethical standards and integrity in professional actions.
Possess the ability to handle sensitive information with confidentiality.
Strong interpersonal and teamwork skills, with the ability to collaborate effectively across teams.
Eager to learn and adapt quickly in a dynamic and fast-paced work environment.
Why Join Us?
At Roche, we endeavor to provide a meaningful and enriching experience that ensures our interns gain valuable industry insights, hands-on knowledge, and the opportunity to build a foundation for their career in regulatory affairs.
What we offer
Roche offers rewarding growth opportunities, a competitive remuneration package and a collaborative culture where people are united in purpose and will stretch you to be brave, speak up and think differently. Feel empowered to deliver meaningful outcomes, supported by accessible and inspiring leaders.
Roche encourages a high-performance culture where you are empowered and trusted to make decisions. We strive for excellence and extraordinary results and take a genuine interest in our people and their well-being, and our patients.
Take pride in knowing you can make a difference to millions of patients worldwide in developing diagnostics and treatments for oncology, neuroscience, inflammation, immunology, ophthalmology, rare diseases, respiratory disease and diabetes.
We are committed to providing an inclusive, safe, secure and healthy workplace, and to minimise any such impacts to our employees, customers and the community. We welcome applications from all people and encourage you to advise of any individual circumstances that may require consideration.
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 27 comparable Intern/Fellow/Postdoc Regulatory Affairs roles across 19 biopharma companies.
Salary context
None of this role's 27 tracked peers disclose a salary range yet.
Where these roles are based
Top locations among the 27 comparable roles
+ 10 more countries
Seniority mix
27 of 27 peers have a known seniority level
Therapeutic area mix
1 of 27 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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.
Open in 2 locations
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Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
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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.