Join Roche as an Associate Regulatory Program Director in Mississauga, Ontario, and contribute to meaningful health solutions. Your role will be pivotal in developing innovative regulatory strategies on a global scale.

In this full-time hybrid position, you will lead efforts to ensure timely product approvals by driving high-quality regulatory submissions and fostering relationships with Health Authorities. You will leverage your significant experience in technical regulatory practices to guide cross-functional teams effectively.

Key Responsibilities: • Oversee submissions of regulatory documents to global health authorities • Lead strategic pre-submission discussions for optimal pathways • Collaborate on the lifecycle management of complex products • Ensure compliance and quality in team deliverables • Respond strategically to regulatory inquiries from authorities

Requirements: • Bachelor’s degree in a relevant life science discipline • At least 5 years in r...