Job Description
ASPHALION is seeking a Regulatory Affairs Consultant / Senior Consultant for its CMC unit. The ideal candidate should have over 5 years of experience in CMC for the pharmaceutical industry, primarily focusing on biologics. Key responsibilities include writing product-specific dossiers, responding to deficiency letters, and managing CMC projects. The role offers a permanent contract, remote work options throughout Spain, and opportunities for training and personal development within a diverse, high-performance environment.
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