The incumbent provides strategic leadership and oversight of a regulatory affairs team responsible for the preparation and submission of applications for the assigned product portfolio across all dosage forms, for products developed and/or manufactured internally or through external partners, supporting the United States and Canadian markets. This role drives regulatory strategy, ensuring timely and compliant preparation, submission, and approval of dossiers to the FDA and Health Canada, while navigating complex regulatory frameworks and evolving guidance. The Director partners externally with development partners and internally, cross functionally with R&D, clinical, quality, manufacturing, and commercial teams to align regulatory objectives with business goals, proactively identify and mitigate regulatory risks, and support successful product submissions, approvals and launches, and subsequent transfer of the product to the product life cycle management (PLCM) department. In addition, the role is accountable for talent development, resource planning, and fostering a high performance regulatory organization that delivers high quality submissions on time and in compliance with applicable regulations.
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Job Type
Full-time
Career Level
Director