Global Medical Device Labeling Specialist

Zimmer Biomet is seeking a Regulatory Affairs professional in Bogotá, Colombia, to lead medical device labeling projects ensuring compliance with global regulations. The candidate should have over 6 years of experience in Regulatory Affairs and a strong understanding of labeling requirements. Responsibilities include collaborating with cross-functional teams and providing regulatory guidance. A Bachelor’s degree in life sciences is preferred. The role offers opportunities for development in an inclusive environment.
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