Join as a Regulatory Affairs Consultant focusing on lifecycle management for five marketed products in Canada. Your expertise will drive effective regulatory submissions and Health Authority interactions.As an experienced consultant, you will provide embedded Canadian Regulatory Affairs support across various products. This role emphasizes developing regulatory strategies, managing submissions, and liaising with Health Authorities for effective interactions.



Your experience with project management and regulatory submissions will be crucial in ensuring timelines and compliance.Key Responsibilities:Provide Canadian Regulatory Affairs support for five productsLead development and management of regulatory submissionsDevelop strategies for complex regulatory submissionsAct as liaison with Canadian Health AuthoritiesManage submission activities throughout the lifecycleRequirements:Robust experience in Canadian Regulatory AffairsFamiliarity with marketed pharmaceutical productsProven ability in submission development and managementExcellent project management and coordination skillsStrong communication and problem-solving capabilitiesUtilize your regulatory expertise to enhance lifecycle management for five key products in Canada.#J-18808-Ljbffr

📌 Lifecycle Management Consultant In Regulatory Affairs (Ottawa)
🏢 G&l Scientific
📍 Ottawa