Roche Posted October 2, 2026

Internship – Agentic AI for Environmental Regulatory Compliance

Basel, Basel-City, Switzerland FULL_TIME
Regulatory Affairs Intern/Fellow/Postdoc
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Roche is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

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

Internship – Agentic AI for Environmental Regulatory Compliance

6 months | Starting December 2026 | Roche Diagnostics  | Location: Basel, Switzerland

Help shape the future of environmental regulatory compliance through Artificial Intelligence.

Are you passionate about Artificial Intelligence, sustainability and applying emerging technologies to real-world challenges?

Join Roche Diagnostics for a six-month internship exploring how agentic AI can transform the way we anticipate, assess and manage environmental regulations affecting medical devices worldwide.

You will be part of the Product Sustainability & Compliance (PS&C) team, working at the intersection of technology, environmental regulation and healthcare innovation. You will collaborate with experts across functions and geographies, gaining hands-on experience in an international, inclusive environment where your ideas and contributions matter.

The Opportunity

You will play an active role in evaluating and piloting an emerging agentic AI platform designed to support global environmental regulatory intelligence and product compliance.

Your impact: Your work will contribute to an evidence-based assessment of the agentic AI platform’s regulatory coverage, accuracy, traceability, reliability, integration potential and business value, helping shape recommendations for future adoption and scalability

Your key responsibilities will include:

Pilot an agentic AI platform: Evaluate its capabilities to identify, interpret and map global environmental regulations applicable to medical devices and in vitro diagnostics.

Develop evaluation criteria: Help define regulatory scope, product categories and relevant product attributes to assess the platform’s performance.

Benchmark AI solutions: Compare the platform with existing tools and selected third-party solutions, assessing regulatory coverage, accuracy, consistency, adaptability to user feedback and overall usability.

Assess business applicability: Evaluate how the platform could integrate with Roche’s existing processes and improve regulatory intelligence, efficiency and compliance readiness.

Translate insights into recommendations: Document key findings, limitations and opportunities, and develop evidence-based recommendations on the platform’s potential value and future adoption.

Who You Are

You are currently enrolled in a Master’s program, preferably in Environmental Engineering, Chemical Engineering, Computational Science or a related discipline.

You bring:

Proficiency with AI tools, data analysis technologies with the ability to critically evaluate their accuracy, reliability and practical applications

Curiosity about environmental regulations, sustainability and healthcare innovation.

An analytical mindset and enthusiasm for solving complex challenges.

The ability to work independently while collaborating effectively with diverse teams.

Strong communication skills and fluency in English.

Prior experience in sustainability, environmental regulatory compliance is an advantage. Curiosity, initiative and willingness to learn are what matter most.

What You Will Gain

Hands-on experience evaluating emerging AI technologies in a global healthcare company.

Exposure to environmental regulations affecting medical devices and diagnostics.

Opportunities to collaborate with regulatory, sustainability, digital and business experts as well as external technology partners

Experience translating technical findings into practical business recommendations.

The opportunity to contribute to how Roche explores AI-enabled regulatory intelligence and compliance.

Application deadline: End of October

We are looking forward to your application!

 

 

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

Seniority
Intern/Fellow/Postdoc
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Basel, Basel-City, Switzerland
Employment type
FULL_TIME

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 37 comparable Intern/Fellow/Postdoc Regulatory Affairs roles across 20 biopharma companies.

37Comparable roles tracked
35Currently active
20Companies hiring similar roles
16Countries represented

Salary context

None of this role's 37 tracked peers disclose a salary range yet.

Where these roles are based

Top locations among the 37 comparable roles

United States11
France5
Germany5
India4
Bulgaria1
Portugal1

+ 10 more countries

Seniority mix

37 of 37 peers have a known seniority level

Intern/Fellow/Postdoc24
Associate13

Therapeutic area mix

2 of 37 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology1
Rare Disease1

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.

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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.

Or follow a whole field: get every new Regulatory Affairs job in Switzerland, and choose locations and companies.

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.

45%
Pharmaziepraktikant*in im Bereich Medical & Scientific Affairs /Regulatory Classics & Compliance für Mai 2028
Sanofi-Aventis Deutschland GmbH · Berlin, Germany · Intern/Fellow/Postdoc
Function Therapeutic area Seniority Country
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Boehringer Ingelheim · Ridgefield, Connecticut, United States · Intern/Fellow/Postdoc
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Unmatched or unknown dimensions score exactly the same: 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.