Chiesi Farmaceutici S.p.A. is seeking a Principal Regulatory Writer for their Global Rare Diseases department in Parma, Italy. This role involves managing regulatory documents for global health authorities, ensuring compliance and quality throughout the drug development lifecycle.
The ideal candidate will possess a relevant advanced degree, fluency in English, and demonstrated experience in regulatory writing. Chiesi offers a comprehensive benefits package and remains committed to diversity and inclusion in the workplace.
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