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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