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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.
As a CMC Regulatory Affairs Intern, you will support the preparation and global filing of critical regulatory submissions to ensure compliance and timely patient access to medicines. Joining our dynamic regulatory affairs team, you will collaborate across functions to manage product lifecycles and uphold global manufacturing quality standards in an inclusive, innovative environment. This role offers a unique opportunity to gain hands-on experience in global commercial registration and post-approval regulatory strategies.
The Opportunity:
Generate and submit high-quality (CMC) regulatory documents to global health authorities.
Ensure strict adherence to current Good Manufacturing Practices (cGMP) and applicable health authority requirements.
Coordinate cross-functional deliverables to ensure regulatory assignments are completed accurately, compliantly, and on schedule.
Monitor project milestones, keeping team leads informed of progress, submission risks, and strategic impacts.
Identify operational efficiencies and contribute to continuous improvement initiatives across regulatory processes.
Support quality system maintenance, health authority commitments, and inspection readiness activities.
Who you are:
You are currently pursuing a Master’s program in Biotechnology, Biomedical Discovery and Commercialization, or a related field.
You possess a solid foundational understanding of the biotechnology/pharmaceutical industry and drug manufacturing processes.
You demonstrate strong written and verbal communication skills with an ability to present clear technical information.
You are a proactive problem solver with a structured, analytical approach to gathering data and making decisions.
You bring strong organizational abilities, learning agility, and a collaborative mindset to thrive in a team environment.
Additional Information:
Term & Location: 12-month full-time internship starting January 2027 in Mississauga, ON (Hybrid model: minimum 3 days in office)
Application: Please submit applications directly via our Workday Portal.
Relocation benefits are not provided.
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We use artificial intelligence to screen, assess or select applicants for this role.
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. 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.
