A pharmaceutical company in Alcobendas is seeking a regulatory affairs professional with expertise in CMC documentation and a solid understanding of global regulatory guidelines.
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The idóneo candidate will have at least 4 years of experience, a relevant scientific degree, and skills in authoring registration applications.
Responsibilities include authoring and reviewing CMC sections, ensuring regulatory compliance, and supporting global registrations. xqysrnh
Strong English proficiency and familiarity with Microsoft Office are essential capabilities.