Bristol Myers Squibb · Giralda, NJ +5 more
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Bristol Myers Squibb seeks a Director of Regulatory CMC for cell therapy to oversee development and lifecycle management projects across multiple sites. The role involves preparing regulatory submissions, representing the company before health authorities, managing cross-functional teams, and directing strategic regulatory direction aligned with global guidelines. Requires a BA/BS degree, minimum 10 years pharmaceutical experience with 8+ years in regulatory CMC, and expertise in advanced therapies and cell therapy development.
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