Global CMC Regulatory Lead - Late-Stage Submissions

A leading pharmaceutical company is seeking an experienced professional in Regulatory Affairs CMC to develop and implement global strategies for small molecule products throughout their lifecycle. The role includes ensuring compliance with FDA, EMA, and ICH regulations, leading regulatory submissions, and engaging with Health Authorities. The ideal candidate has over 7 years of experience, a strong educational background in chemistry or pharmacy, and excellent analytical and communication skills.

This position requires some domestic and international travel, with a competitive salary range between $ to $.
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