Experteer Italy is seeking a Regulatory Affairs Specialist to manage CMC dossier preparations and submissions worldwide. This role involves working with cross-functional teams to translate technical reports into regulatory documents and ensuring compliance with GMP, ICH, EMA, and WHO guidelines.
The ideal candidate should have over 3 years of experience in regulatory CMC affairs, strong skills in crafting Module3 content, and a deep understanding of regulatory frameworks. Join us to make a meaningful impact in compliance and lifecycle management.
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📌 Module3 CMC Specialist — Global Submissions (Italia)
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📍 Italia