Senior Regulatory Cmc Consultant Veeva Rim

Apply senior regulatory CMC expertise to small-molecule pharmaceuticals using Veeva RIM in a Canada-based consulting assignment. Support compliance, reporting, and surveillance.This senior consultant supports regulatory affairs for small-molecule products throughout their lifecycle. You will interpret North American requirements, assess guidelines, and apply drug development knowledge. The work includes organized project execution, clear communication, and collaboration with cross-functional teams.Key Responsibilities:
Support small-molecule regulatory affairs and CMC activitiesApply North American requirements to product complianceContribute to reporting and ongoing market surveillanceInterpret guidelines and provide practical recommendationsCommunicate findings across technical and non-technical stakeholdersRequirements:
Degree in a life sciences discipline preferredTypically eight years pharmaceutical or biotechnology experienceStrong North American regulatory affairs knowledgePractical Veeva RIM experience specifically requiredExcellent communication and organizational skillsBring Veeva RIM, small-molecule CMC, and North American regulatory expertise to senior consulting projects in Canada.
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