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Teleflex is seeking a Regulatory Affairs Specialist based in Johannesburg to support regulatory activities for medical products in the EMEA region. Responsibilities include managing regulatory submissions, providing timely regulatory inputs for projects, and ensuring compliance with international
Overview Support the regulatory activities which lead to and maintain regulatory compliance and approval for Teleflex Medical products in the EMEA region. Principal Responsibilities Coordination and management of regulatory and product registration activities for the EMEA region
