Italfarmaco is seeking an experienced candidate in Alcobendas, Spain to author and review CMC sections for drug registration applications. The role focuses on ensuring regulatory compliance and supporting quality assessments throughout the product lifecycle.
Adecuado candidates will have at least 4 years of CMC experience, a degree in a relevant scientific discipline, and strong attention to detail. This position offers the opportunity to work in a dynamic environment with a focus on team collaboration and regulatory strategies.
📌 CMC Regulatory Writer - Global Submissions & Compliance (Madrid)
🏢 ITALFARMACO
📍 Madrid
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