A global biopharmaceutical consulting firm is seeking an experienced CMC Regulatory Affairs Senior/Consultant to join their team in Augusta, ME. The role focuses on providing regulatory strategy and support for new and marketed small-molecule and biologic products. Responsibilities include preparing regulatory submissions, collaborating with cross-functional teams, and ensuring compliance with global regulatory standards. The ideal candidate has 4-6 years of regulatory experience, effective communication skills, and a strong understanding of drug development processes. This position offers opportunities for innovation in the regulatory field.
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