Global CMC Regulatory Director

A clinical-stage biopharmaceutical company is looking for an experienced regulatory CMC professional to manage submissions and oversee compliance with global regulatory guidelines. The ideal candidate will have a Ph.D. and significant experience in CMC lifecycle management within the biotech/pharma sector. This role involves leading FDA meetings, ensuring timely submissions, and collaborating with project teams to achieve corporate goals. Strong communication and project management skills are essential. Attractive compensation package offered.
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