Drive regulatory success at Teva Pharmaceuticals in Scarborough as their Manager of Regulatory Affairs in a hybrid capacity. Oversee strategic planning and Health Canada submission processes for generics.
This role at Teva Pharmaceuticals involves leading Canadian regulatory affairs for various pharmaceutical products. You’ll be instrumental in managing ANDS submissions, ensuring compliance with Health Canada standards, and fostering communication with global teams to support drug launches. Your regulatory expertise will contribute to maintaining high standards of product safety and efficacy.
Key Responsibilities:
• Prepare and maintain ANDSs and sANDSs submissions
• Ensure compliance through timely labelling updates
• Manage response timelines for regulatory reviews
• Lead regulatory meetings for submission readiness
• Collaborate with local and global project teams
Requirements:
• Bachelor's in a science-related field; Master’s preferred
• Minimum 5 year...