Support Italian medical device manufacturers in obtaining MENA regulatory approvals (MOHAP UAE, SFDA Saudi, Egyptian Drug Authority). The role involves preparing technical dossiers, managing authority submissions, and monitoring post-market compliance.

Requirements

Degree in biomedical engineering, pharmacy, or life sciences. 3+ years in medical device regulatory affairs. Knowledge of MENA health authority processes. English required.

Benefits

Flexible hybrid work. Professional development. Annual bonus. Private health cover.

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Business Sectors

Healthcare, Biotechnology and Life Sciences

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