Elevate your career as a Regulatory Affairs Consultant, offering lifecycle management expertise for five key products marketed in Canada. Engage deeply with regulatory submissions and Health Authority processes.In this embedded consultancy role, you will leverage your strong background in Canadian regulatory affairs to guide regulatory submissions and ensure successful Health Authority interactions. Your strategic approach and ability to coordinate complex activities will be pivotal in managing the regulatory lifecycle of marketed products.Key Responsibilities:Provide embedded support in Regulatory Affairs for five productsDevelop and manage submissions tailored to regulatory needsCoordinate interactions with the Canadian Health AuthorityManage timelines and cross-functional regulatory deliverablesOffer continuous regulatory advice for lifecycle managementRequirements:Deep experience in Canadian Regulatory AffairsExperience in pharmaceutical lifecycle managementProven submission management skillsExcellent project and stakeholder coordination capabilitiesStrong communication and problem-solving skillsJoin our endeavor to enhance compliance and regulatory strategies for significant pharmaceutical products.

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