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