Advance your skills at Roche as a Pharma Technical Regulatory Submission Intern in Mississauga. This role offers a hybrid work workplace with a focus on submissions and regulatory excellence.
This 12-month internship at Roche enables you to engage with critical submission processes while maintaining compliance in the pharmaceutical sector. Work alongside experts and refine your capabilities in project management and data systems, directly contributing to improved patient care outcomes. Your role will help ensure high-quality regulatory submissions on a global scale.
Key Responsibilities:
• Prepare global regulatory submissions and CTD dossiers • Coordinate documentation for various health authority submissions • Develop project timelines to enhance regulatory workflows • Implement data quality management in IT systems • Liaise with technical teams for regulatory support
Requirements: • Currently pursuing a Master's in Biotechnology or related field • Understanding of drug development and industry processes • Proven detail orientation and proofreading skills • Comfortable with digital tools for workflow efficiency • Strong organizational and communication skills
Contribute to Roche's mission of innovative healthcare solutions and build your expertise in regulatory operations. #J-18808-Ljbffr