Regulatory Affairs IVDR - Contractor Côte d'Ivoire
IQVIA · Ivory Coast
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Role summary
IQVIA seeks an experienced regulatory contractor based in Côte d'Ivoire to support IVDR transition projects and regulatory activities across the EMEA region. The role involves managing product registrations, import notifications, change control projects, and regulatory compliance for in vitro diagnostics, working collaboratively with cross-functional teams. Candidates require minimum 2 years' medical device regulatory affairs experience, strong project management skills, fluent English, and knowledge of local regulatory environments.
Privacy & handoff
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