EMEA Regulatory CMC Lead - Strategy & Submissions

A biotech company focused on rare diseases is seeking a Senior Manager, Regulatory Affairs CMC in Switzerland. You will lead the development of regulatory strategies and manage submissions for clinical and marketing applications in the EMEA region. Ideal candidates should have over 6 years of experience in Regulatory Affairs CMC, with a thorough understanding of drug development regulations and proven success in interacting with health authorities.

This is a full-time role requiring hybrid work model, emphasizing professional growth and patient impact.
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