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 regulations. The ideal candidate will have a degree in a relevant discipline, 2-3 years of experience in the medical device industry, and project management skills. Teleflex offers a dynamic work environment with opportunities for growth.#J-18808-Ljbffr
Senior Emea Regulatory Affairs Specialist
TELEFLEX
city of johannesburg metropolitan municipality, city of johannesburg metropolitan municipality
Published 27 days ago
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