CMC Documentation Manager - Regulatory Submissions Lead
Bristol-Myers Squibb
Bristol-Myers Squibb is seeking a Manager for CMC Documentation in New Brunswick, NJ. The role involves compiling and authoring CMC sections of regulatory submissions, coordinating with various teams to ensure timely document delivery. Ideal candidates will have a degree in organic chemistry or related fields along with at least 5 years of experience in pharmaceutical development. Strong communication skills and familiarity with document preparation tools are essential. This position offers competitive compensation and a variety of benefits to support a flexible work-life balance. #J-18808-Ljbffr
Vacancy posted 1 day ago
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