Launch your career with Roche as a Regulatory Submission Intern in Mississauga. This hybrid internship emphasizes regulatory compliance and submission processes, making a real-world impact.
Join Roche for a 12-month internship focused on producing high-quality regulatory submissions for health authorities. Collaborate with cross-functional experts and learn essential skills in project management and data systems while contributing to lifesaving outcomes in healthcare. Your role will be integral to operational excellence in the pharmaceutical industry.
Key Responsibilities:
• Prepare CMC regulatory submissions including Module 3 documents
• Manage diverse regulatory submission documentation
• Create and monitor timelines for regulatory operations
• Utilize data quality practices and IT support
• Assist technical teams with clear regulatory direction
Requirements:
• Pursuing a Master's degree in Biotechnology or similar
• Familiarity with industry operations in drug development
• Detail-oriented with solid proofreading abilities
• Proficient in leveraging digital tools for efficiency
• Effective communicator and organized team player
Join Roche and be part of a global mission for better healthcare.
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