Hybrid CMC RA Lead — Biologics & Biosimilars

A leading consultancy in the pharmaceutical industry is seeking a Regulatory Affairs Senior Officer to join their CMC unit. The role involves managing global CMC writing, supporting responses to regulatory deficiency letters, and liaising with various teams during drug development. Ideal candidates will have at least 4 years of experience in Regulatory Affairs, specializing in biologics, and must be fluent in English and Spanish. This position offers a permanent contract and a hybrid work model across Spain.

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