About the role#
This is a full-time, paid internship for the Winter 2027 term. You will support the Regulatory Affairs team in Mississauga, working on submissions to Health Canada and collaborating with local and global stakeholders to ensure regulatory compliance.
What you'll do#
- Prepare regulatory submissions including Clinical Trial Applications, New Drug Submissions, and Medical Device Applications.
- Participate in publishing activities and draft responses to Health Canada queries.
- Attend cross-functional meetings to support regulatory projects.
- Develop and maintain Canadian Standard Operating Procedures, process maps, and operating guides.
- Manage internal electronic document management systems and departmental information-sharing frameworks like gDrives, gSites, and OneArchive.
- Stay informed on Canadian regulations and contribute to process optimization objectives.
What you'll need#
- A Bachelor’s Degree in Science.
- Current enrollment in a post-graduate program, specifically Humber College’s Regulatory Affairs program or Seneca College’s Pharmaceutical Regulatory Affairs & Quality Operations program.
- A general understanding of Health Canada regulations and guidelines.
- Proficiency in Microsoft Office and Google Suite.
- A basic understanding of automation and artificial intelligence applications such as OpenAI, Microsoft CoPilot, Notebook LM, and Gemini.
- Strong skills in communication, problem-solving, project management, and planning.
Location & details#
- Location: Mississauga, Ontario.
- Modality: Hybrid, with a minimum of 3 days per week in the office.
- Term: 12 months, beginning in January 2027.
About Roche
Roche operates as a global pharmaceutical and diagnostics company. It focuses on oncology, immunology, infectious diseases, and ophthalmology. The company maintains a presence in the central nervous system disease space and diabetes management. It employs over 100,000 people and maintains its headquarters in Switzerland.
How to get in at Roche
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