Regulatory Affairs Intern — Roche
- Location
- La Roche
- Contract
- full-time
- Posted
- 3 days ago
Role overview
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.
- 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.
Application process
- Our strategic focus is on building, submitting, and obtaining approvals for clinical trial applications, new drug submissions, and new indications.
- Additionally, we collaborate with external partners to shape regulatory policies that eliminate barriers, enabling faster access to medications and therapies for patients. The Opportunity
- Supports the Regulatory Affairs team in the preparation of various regulatory submissions to Health Canada (ie, Clinical Trial Applications and Amendments, Investigational Testing Authorizations, New Drug Submissions, Medical Device Applications, Supplemental New Drug Submissions, Notifiable Changes, and Level III Changes), publishing activities, and responses to Health Canada queries.
- Responsible for actively participating in cross-functional meetings for regulatory submissions, working closely with relevant local and global stakeholders (Product Development Regulatory, Pharma Technical Regulatory, Product Development Operations, GxP, etc.)
- Accountable for keeping up-to-date with evolving Canadian Regulations to facilitate decision-making and ensure regulatory compliance
- Contributes to the development and maintenance of Canadian Standard Operating Procedures (SOPs), process maps, and operating guides that are aligned to our Canadian regulatory requirements (Food and Drug Act and Regulations; Medical Device Regulations)
- Keeps up to date on relevant internal electronic document management systems used for regulatory projects to be able to efficiently execute day-to-day activities (eg.
- Regulatory Information Management System etc), and supports cross-functional processes
Additional details
- Join Roche, where every voice matters.
- Additionally, we collaborate with external partners to shape regulatory policies that eliminate barriers, enabling faster access to medications and therapies for patients.
- Contributes to the development and maintenance of Canadian Standard Operating Procedures (SOPs), process maps, and operating guides that are aligned to our Canadian regulatory requirements (Food and Drug Act and Regulations; Medical Device Regulations)
- Participates in departmental objectives pertaining to process optimization You hold a Bachelor’s Degree in Science
- Seneca College’s Pharmaceutical Regulatory Affairs & Quality Operations program)
- Basic understanding of automation and artificial intelligence (AI) concepts and applications (ie, OpenAI, Microsoft CoPilot, Notebook LM, Gemini) Additional Information:
- This posting is for an existing vacancy at Hoffmann-La Roche Ltd. 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.
Notes and original content
- The Position
- The Opportunity
- Contributes to the development and maintenance of Canadian Standard Operating Procedures (SOPs), process maps, and operating guides that are aligned to our Canadian regulatory requirements (Food and Drug Act and Regulations;
- Medical Device Regulations)
- Participates in departmental objectives pertaining to process optimization
- Who you are:
- You hold a Bachelor’s Degree in Science
- Basic understanding of automation and artificial intelligence (AI) concepts and applications (ie, OpenAI, Microsoft CoPilot, Notebook LM, Gemini)
- Additional Information:
- This posting is for an existing vacancy at Hoffmann-La Roche Ltd.
Questions about this listing
What salary does Roche offer for this role?
Roche lists CHF 52'000 - 78'500 gross per year for this position in La Roche. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Roche offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Roche during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Fribourg?
EU/EFTA residents living in the border zone of the country adjoining Canton Fribourg can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Fribourg's cantonal migration office or with HR during the application.
How do I apply for this position at Roche?
Use the "Apply now" button on this page — it links directly to Roche's original listing at roche.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
