Enhance your career with Roche as a Pharma Technical Regulatory Submission Intern in Mississauga. This hybrid internship focuses on regulatory submissions and compliance, fostering expertise in vital processes.
At Roche, you will contribute to global regulatory submissions, joining a diverse team in a 12-month internship. Gain experience in project management, data systems, and regulatory operations while ensuring adherence to health authority standards. Your role is crucial for driving quality patient outcomes and cooperative work.
Key Responsibilities:
• Prepare global CMC regulatory submissions and CTD dossiers
• Manage regulatory documentation for health authority submissions
• Create and maintain project timelines for regulatory processes
• Apply data quality management practices in IT systems
• Collaborate with technical development teams for regulatory guidance
Requirements:
• Enrolled in a Master's degree in Biotechnology or related field
• Knowledge of pharmaceutical operations and drug development
• Strong attention to detail and proofreading skills
• Tech-savvy with a focus on digital tools for workflow
• Excellent organizational and communication skills
Develop your expertise in regulatory processes and support Roche's mission in creating a healthier future.
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