Senior Regulatory Writer, Global Rare Diseases

01 ago - Italia
Biotecnologie - Farmacia - Chimica

Chiesi Farmaceutici S.p.A. seeks a Principal Regulatory Writer in Parma to author and manage regulatory documents for global health authorities such as FDA and EMA. The role involves collaboration with diverse teams to ensure compliance across the product lifecycle.
Candidates should have a relevant life science degree, experience in regulatory writing, and fluency in English. A strong understanding of regulatory frameworks and document structures is crucial. A competitive package including salary and benefits is offered.
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