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 authoritiesRequirements: • Bachelor’s degree in a relevant life science discipline • At least 5 years in regulatory, manufacturing, or quality sectors • Knowledge of biologics manufacturing is highly desired • Experience in regulatory strategy development • Strong leadership and organizational skillsMake an impact in global healthcare through your regulatory leadership at Roche. #J-18808-Ljbffr
Associate Director Of Regulatory Programs - Roche
F. HOFFMANN-LA ROCHE GRUPPE
mississauga, mississauga
Published 18 days ago
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