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 i...